Patent Application
20230097883
L-ergothioneine (ERGO) is a food-derived hydrophilic antioxidant available in fungi and various bacteria, but not in animals or higher plants. It has been known as an antioxidant since its discovery a century ago from fungi of the genus Claviceps purpurea. Chemically, this rare betaine-based amino acid has a similar chemical structure to histidine but with the presence of a sulfhydryl moiety on the imidazole ring. The molecule exists as a tautomeric form between thioketone and thiol derivatives (
ERGO is also implicated in a number of neurological pathways. Substantial research data indicate that ERGO is a physiological antioxidant cytoprotectant. Protection against cytotoxicity elicited by Cu (II), hydrogen peroxide, iron, and sodium nitrite is derived from the conspicuous affinity of ERGO for metal cations, such as Fe and Cu, permitting capture and neutralization of associated radicals. It has been demonstrated that ERGO concentration decreases significantly with age, and markedly lower levels were found in individuals with mild cognitive impairment compared to the controls, supporting the potential for ERGO deficiency to act as a risk factor for neurodegeneration. It is worthwhile to mention that ERGO does not permeate the blood-brain barrier (BBB); its uptake in cells is mediated by an OCTN1 (organic cation transporter novel, type 1) receptor. Other studies have shown that ERGO can protect neurons both in vitro and in vivo against a spectrum of stressors. Taken altogether, these data strongly suggest that ERGO is involved in healthy aging, serving as a “longevity vitamin”. The term “vitamin” is used in here since ERGO is a micronutrient, that the body does not need a lot of to function, but the material needs to be constantly available by uptake from an external source such as foods or supplements and it therefore does fit into that category.
To date, all preclinical studies had relied solely on in vitro analysis of ERGO using analytical and bioassay methods for analyzing the ERGO distribution from extracted tissues. The same holds true for clinical studies to validate the benefit of ERGO consumption in the diet; serum samples were collected for assessing the ERGO levels.
Embodiments of the present disclosure relates to ergothioneine PET compounds and methods of use thereof. In particular, the presently disclosed subject matter relates to ergothioneine PET analogs and imaging methods using these compounds.
The present disclosure provides for an ergothioneine (ERGO) based positron emission tomography (PET) probe having the following structure:
wherein n is 1, 2, or 3, wherein R1 is an alkyl group.
The present disclosure provides for a pharmaceutical composition, comprising: a pharmaceutical carrier and an effective dose of ergothioneine (ERGO) based positron emission tomography (PET), wherein the ERGO PET probe has the following structure:
where n is 1, 2, or 3, where R1 is an alkyl group.
The present disclosure provides for a precursor compound for ergothioneine (ERGO) based positron emission tomography (PET) probe having the following structure:
wherein n is 1, 2, or 3, wherein R1 is an alkyl group. The present disclosure also includes a kit comprising the precursor compound for ERGO PET probe
The present disclosure provides for a method of imaging an inflammatory disease in a subject comprising: administering to a subject a labeled probe in a detectably effective amount, wherein the labeled probe is ergothioneine (ERGO) based positron emission tomography (PET) probe having the following structure:
wherein n is 1, 2, or 3, wherein R1 is an alkyl group; imaging at least a portion of the subject; and detecting the labeled probe, wherein the location of the labeled probe corresponds to inflammation corresponding to the inflammatory disease.
The present disclosure provides for a composition, comprising:
wherein n is 1, 2, or 3, wherein R1 is an alkyl group.
The present disclosure provides for a pharmaceutical composition, comprising: a pharmaceutical carrier and an effective dose of
wherein n is 1, 2, or 3, wherein R1 is an alkyl group.
The presently disclosed subject matter will be better understood, and features, aspects and advantages other than those set forth above will become apparent when consideration is given to the following detailed description thereof. Such detailed description makes reference to the following drawings, wherein:
While the disclosure is susceptible to various modifications and alternative forms, specific embodiments thereof have been shown by way of example in the drawings and are herein described below in detail. It should be understood, however, that the description of specific embodiments is not intended to limit the disclosure to cover all modifications, equivalents and alternatives falling within the spirit and scope of the disclosure as defined by the appended claims.
In general, the present disclosure relates to ergothioneine PET compounds and methods of use thereof. In particular, the presently disclosed subject matter relates to ergothioneine PET analogs and imaging methods using these compounds.
This disclosure is not limited to particular embodiments described, and as such may, of course, vary. The terminology used herein serves the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present disclosure will be limited only by the appended claims.
Where a range of values is provided, each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the disclosure. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges and are also encompassed within the disclosure, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure.
As will be apparent to those of skill in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several embodiments without departing from the scope or spirit of the present disclosure. Any recited method may be carried out in the order of events recited or in any other order that is logically possible.
Embodiments of the present disclosure will employ, unless otherwise indicated, techniques of chemistry, medical imaging, biochemistry, pharmacology, medicine, and the like, which are within the skill of the art. Such techniques are explained fully in the literature.
Prior to describing the various embodiments, the following definitions are provided and should be used unless otherwise indicated.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art of microbiology, molecular biology, medicinal chemistry, physical chemistry, and/or organic chemistry. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present disclosure, suitable methods and materials are described herein.
As used in the specification and the appended claims, the singular forms “a,” “an,” and “the” may include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a support” includes a plurality of supports. In this specification and in the claims that follow, reference will be made to a number of terms that shall be defined to have the following meanings unless a contrary intention is apparent.
In describing and claiming the disclosed subject matter, the following terminology will be used in accordance with the definitions set forth below.
By “administration” or “administering” is meant introducing an ergothioneine (ERGO) based positron emission tomography (PET) probe (or compound), analogs thereof, compositions and pharmaceutical compositions including the ERGO PET probe of the present disclosure into a subject. The preferred route of administration of the compounds is intravenous. However, any route of administration, such as oral, topical, subcutaneous, peritoneal, intraarterial, inhalation, vaginal, rectal, nasal, introduction into the cerebrospinal fluid (e.g., intrathecal), or instillation into body compartments can be used.
As used herein, “alkyl” or “alkyl group” refers to a saturated aliphatic hydrocarbon radical which can be straight or branched and/or substituted or unsubstituted, having 1 to 6 carbon atoms (C1-C6) or 1 to 4 carbon atoms (C1-C4), wherein the stated range of carbon atoms includes each intervening integer individually, as well as sub-ranges. Examples of alkyl include, but are not limited to methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, n-pentyl, and sec-pentyl, and the like.
In accordance with the present disclosure, “a detectably effective amount” of the ERGO PET probe or compositions (e.g., pharmaceutical compositions) including the ERGO PET probe of the present disclosure is defined as an amount sufficient to yield an acceptable image using equipment that is available for clinical use. A detectably effective amount of the ERGO PET probe or compositions including the ERGO PET probe of the present disclosure may be administered in more than one injection. The detectably effective amount of the ERGO PET probe or compositions including the ERGO PET probe of the present disclosure can vary according to factors such as the degree of susceptibility of the individual, the age, sex, and weight of the individual, idiosyncratic responses of the individual, and the like. Detectably effective amounts of the ERGO PET probe or compositions including the ERGO PET probe of the present disclosure can also vary according to instrument and film-related factors. Optimization of such factors is well within the level of skill in the art.
As used herein, the term “subject” includes vertebrates such as humans and mammals (e.g., cats, dogs, horses, etc.). Typical subjects to which embodiments of the present disclosure may be administered will be mammals, particularly primates, especially humans. For veterinary applications, a wide variety of subjects will be suitable, e.g., livestock such as cattle, sheep, goats, cows, swine, and the like; poultry such as chickens, ducks, geese, turkeys, and the like; and domesticated animals particularly pets such as dogs and cats. For diagnostic or research applications, a wide variety of mammals will be suitable subjects, including rodents (e.g., mice, rats, hamsters), rabbits, primates, and swine such as inbred pigs and the like. Additionally, for in vitro applications, such as in vitro diagnostic and research applications, body fluids and cell samples of the above subjects will be suitable for use, such as mammalian (particularly primate such as human) blood, urine, or tissue samples, or blood, urine, or tissue samples of the animals mentioned for veterinary applications. In some embodiments, a system includes a sample and a subject. The term “living subject” refers to a subject noted above that is alive and is not dead. The term “living subject” refers to the entire subject and not just a part excised (e.g., a liver or other organ) from the living subject.
The term “detectable” refers to the ability to detect a signal over the background signal.
The term “detectable signal” is a signal derived from non-invasive imaging techniques such as, but not limited to, positron emission tomography (PET). The detectable signal is detectable and distinguishable from other background signals that may be generated from the subject. In other words, there is a measurable and statistically significant difference (e.g., a statistically significant difference is enough of a difference to distinguish among the detectable signal and the background, such as about 0.1%, 1%, 3%, 5%, 10%, 15%, 20%, 25%, 30%, or 40% or more difference between the detectable signal and the background) between the detectable signal and the background. Standards and/or calibration curves can be used to determine the relative intensity of the detectable signal and/or the background.
The term “pharmaceutically acceptable carrier” as used herein refers to a diluent, adjuvant, excipient, or vehicle with which the ERGO PET probe or compositions including the ERGO PET probe of the disclosure is administered and which is approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans. Such pharmaceutical carriers can be liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like. The pharmaceutical carriers can be saline, gum acacia, gelatin, starch paste, talc, keratin, colloidal silica, urea, and the like. When administered to a patient, the ERGO PET probe or compositions including the ERGO PET probe of the disclosure and pharmaceutically acceptable carriers preferably should be sterile. Water is a useful carrier when the ERGO PET probe or compositions including the ERGO PET probe of the disclosure is administered intravenously. Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers, particularly for injectable solutions. Suitable pharmaceutical carriers also include excipients such as glucose, lactose, sucrose, glycerol monostearate, sodium chloride, glycerol, propylene, glycol, water, ethanol and the like. The present compositions, if desired, can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents. The present compositions advantageously may take the form of solutions, emulsion, sustained-release formulations, or any other form suitable for use.
The disclosure encompasses compositions and dosage forms of the compositions of the disclosure that can include one or more compounds that reduce the rate by which an active ingredient will decompose. Such compounds, which are referred to herein as “stabilizers,” include, but are not limited to, antioxidants such as ascorbic acid, pH buffers, or salt buffers. In addition, pharmaceutical compositions or dosage forms of the disclosure may contain one or more solubility modulators, such as sodium chloride, sodium sulfate, sodium or potassium phosphate, or organic acids. An exemplary solubility modulator is tartaric acid.
“Pharmaceutically acceptable salt” refers to those salts that retain the biological effectiveness and properties of the free bases and that are obtained by reaction with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, malic acid, maleic acid, succinic acid, tartaric acid, citric acid, and the like.
Embodiments of the present disclosure include pharmaceutical compositions that include the ERGO PET probe, pharmaceutically acceptable salts thereof, with other chemical components, such as physiologically acceptable carriers and excipients. One purpose of a pharmaceutical composition is to facilitate administration of the ERGO PET probe to a subject (e.g., human).
Embodiments of the present disclosure may be salts and these salts are within the scope of the present disclosure. Reference to a compound of any of the formulas herein is understood to include reference to salts thereof, unless otherwise indicated. The term “salt(s)”, as employed herein, denotes acidic and/or basic salts formed with inorganic and/or organic acids and bases. In addition, when an embodiment of the present disclosure contains both a basic moiety and an acidic moiety, zwitterions (“inner salts”) may be formed and are included within the term “salt(s)” as used herein. Pharmaceutically acceptable (e.g., non-toxic, physiologically acceptable) salts are preferred, although other salts are also useful, e.g., in isolation or purification steps which may be employed during preparation. Salts of the compounds may be formed, for example, by reacting an active compound with an amount of acid or base, such as an equivalent amount, in a medium such as one in which the salt precipitates or in an aqueous medium followed by lyophilization.
Embodiments of the present disclosure that contain a basic moiety may form salts with a variety of organic and inorganic acids. Exemplary acid addition salts include acetates (such as those formed with acetic acid or trihaloacetic acid, for example, trifluoroacetic acid), adipates, alginates, ascorbates, aspartates, benzoates, benzenesulfonates, bisulfates, borates, butyrates, citrates, camphorates, camphorsulfonates, cyclopentanepropionates, digluconates, dodecylsulfates, ethanesulfonates, fumarates, glucoheptanoates, glycerophosphates, hemisulfates, heptanoates, hexanoates, hydrochlorides (formed with hydrochloric acid), hydrobromides (formed with hydrogen bromide), hydroiodides, 2-hydroxyethanesulfonates, lactates, maleates (formed with maleic acid), methanesulfonates (formed with methanesulfonic acid), 2-naphthalenesulfonates, nicotinates, nitrates, oxalates, pectinates, persulfates, 3-phenylpropionates, phosphates, picrates, pivalates, propionates, salicylates, succinates, sulfates (such as those formed with sulfuric acid), sulfonates (such as those mentioned herein), tartrates, thiocyanates, toluenesulfonates such as tosylates, undecanoates, and the like.
Embodiments of the present disclosure that contain an acidic moiety may form salts with a variety of organic and inorganic bases. Exemplary basic salts include ammonium salts, alkali metal salts such as sodium, lithium, and potassium salts, alkaline earth metal salts such as calcium and magnesium salts, salts with organic bases (for example, organic amines) such as benzathines, dicyclohexylamines, hydrabamines (formed with N,N-bis(dehydroabietyl)ethylenediamine), N-methyl-D-glucamines, N-methyl-D-glucamides, t-butyl amines, and salts with amino acids such as arginine, lysine, and the like.
Basic nitrogen-containing groups may be quaternized with agents such as lower alkyl halides (e.g., methyl, ethyl, propyl, and butyl chlorides, bromides and iodides), dialkyl sulfates (e.g., dimethyl, diethyl, dibutyl, and diamyl sulfates), long chain halides (e.g., decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides), aralkyl halides (e.g., benzyl and phenethyl bromides), and others.
Solvates of the compounds of the disclosure are also contemplated herein. Solvates of the compounds are preferably hydrates.
The amounts and a specific type of active ingredient (e.g., the ERGO PET probe or compositions including the ERGO PET probe) in a dosage form may differ depending on various factors. It will be understood, however, that the total daily usage of the ERGO PET probe or compositions including the ERGO PET probe of the present disclosure will be decided by the attending physician or other attending professional within the scope of sound medical judgment. The specific effective dose level for any particular subject will depend upon a variety of factors, including for example, the activity of the specific composition employed; the specific composition employed; the age, body weight, general health, sex, and diet of the subject; the time of administration; the route of administration; the rate of excretion of the specific compound employed; the duration of the treatment; the existence of other drugs used in combination or coincidental with the specific composition employed; and like factors well known in the medical arts. For example, it is well within the skill of the art to start doses of the ERGO PET probe or compositions including the ERGO PET probe at levels lower than those required to achieve the desired effect and to gradually increase the dosage until the desired effect is achieved.
The term “positron emission tomography” as used herein refers to a nuclear medicine imaging technique that produces a three-dimensional image or map of functional/molecular processes in the body. The system detects pairs of gamma rays emitted indirectly by a positron-emitting radioisotope, which is introduced into the body via a molecule specific for a target/process of interest. Images of the target/process of interest in space are then reconstructed by computer analysis. Using statistics collected from tens-of-thousands of coincidence events, a set of simultaneous equations for the total activity of each parcel of tissue can be solved by a number of techniques, and a map of radioactivities as a function of location for parcels or bits of tissue may be constructed and plotted. The resulting map shows the tissues in which the molecular probe has become concentrated. PET technology can be used to trace the biologic pathway of any compound in living humans (and many other species as well), provided it can be radiolabeled with a PET isotope.
The term “label” as used herein refers to any moiety that may be linked (e.g. bonded or otherwise associated with) to the agent (e.g., antibody of TREM-1) of the present disclosure and which may be used to provide a detectable image including, but not limited to, a radiolabel such as a PET probe.
The term “in vivo imaging” as used herein refers to methods or processes in which the structural, functional, molecular, or physiological state of a living being is examinable without the need for a life-ending sacrifice.
The term “non-invasive in vivo imaging” as used herein refers to methods or processes in which the structural, functional, molecular, or physiological state of being is examinable by remote physical probing without the need for breaching the physical integrity of the outer (skin) or inner (accessible orifices) surfaces of the body.
Embodiments of the present disclosure include compounds and probes such as ergothioneine (ERGO) based positron emission tomography (PET) (ERGO PET) probes or compounds or compositions including the ERGO PET probe such as pharmaceutical compositions, methods of making the ERGO PET probes or compositions, methods of imaging using the ERGO PET probes or compositions, and the like. The present disclosure provides for ERGO PET probes or compositions that can be used for imaging, diagnosing, localizing, monitoring, and/or assessing neurodegenerative diseases and inflammatory diseases or related biological conditions, to monitor the progression (or regression) of the inflammatory diseases, or to assess the response of the inflammatory diseases to treatment, and the like. In an aspect, the neurodegenerative diseases and inflammatory diseases can include, but not limited to, Alzheimer's disease (AD), sepsis, sepsis induced encephalopathy (SIE), multiple sclerosis, epilepsy, traumatic brain injury, cancer, arthritis, inflammatory bowel diseases (e.g., colitis), Huntington's disease, Amytrophic Lateral Sclerosis (ALS), Parkinson's disease, infectious diseases, pain, stroke, chronic fatigue syndrome, depression, schizophrenia, other central nervous system and peripheral inflammatory diseases, or related biological events.
Embodiments of the present disclosure include methods for imaging a sample (e.g., tissue or cell(s)) or a subject, that includes contacting a sample with or administering to a subject ERGO PET probes or compositions and imaging the sample with a PET imaging system. Imaging can be performed in vivo, ex vivo, and/or in vitro. In particular, embodiments of the present disclosure can be used to image neurodegenerative diseases and inflammatory diseases or related biological events. In this regard, the sample or subject can be tested to determine if the sample or subject includes inflammation or related biological conditions, to monitor the progression (or regression) of the inflammation, or to assess the response of the inflammation to treatment, and the like. In an embodiment, the tissue or cells can be within a subject or can have been removed from a subject. In particular, the present disclosure includes methods relating to non-invasive imaging (e.g., using positron emission tomography (PET) imaging system) using the ERGO PET probes or compositions in vivo.
In an embodiment, the ERGO PET probes or compositions can be imaged using imaging systems such as a positron emission tomography (PET) imaging systems (and combined PET/CT and PET/MR systems) or an ex vivo/in vitro phosphor imager. In an embodiment, PET imaging is a preferred embodiment.
In contrast to many other compounds that cannot enter the brain, ERGO PET probes or compositions of the present disclosure are actively transported into the brain by OCTN1 receptors. Since the ERGO PET probes or compositions are actively transported by the OCTN1 receptors, in some embodiments, the method includes mapping OCTN1 receptors within the subject. Additionally or alternatively, in some embodiments, the method includes monitoring concentration in specific regions of the brain and/or body through administration to the subject and imaging of the ERGO PET probes or compositions. For example, in one embodiment, the method includes monitoring concentration of the ERGO PET probes or compositions in the cortex and cerebellum of the subject. In another embodiment, the method includes monitoring concentration of the ERGO PET probes or compositions in the eyes of the subject. In a further embodiment, the method includes monitoring concentration of the ERGO PET probes or compositions in the small intestine.
In addition to being actively transported through the OCTN1 receptors, the ERGO PET compounds disclosed herein bind to and/or react with oxidants and/or amyloid plaques. Accordingly, in some embodiments, the method includes detecting inflammation and/or amyloid plaques using methods as provided herein. As amyloid plaques are implicated in various neurodegenerative diseases, such as Alzheimer's disease, in some embodiments, the method includes detecting and/or diagnosing a subject with a neurodegenerative disease. In such embodiments, the method includes administering the ERGO PET probes or compositions to a subject, monitoring the distribution of the ERGO PET probes or compositions following administration, and diagnosing the subject with a neurodegenerative disease based upon the identification of amyloid plaques. Similarly, the method may include monitoring response to therapy by detecting changes in the presence of amyloid plaques (e.g., increase or decrease in the number or size of plaques).
Furthermore, as ERGO PET probes or compositions disclosed herein may remove oxidants and/or amyloid plaques, in some embodiments, the method includes treating a neurodegenerative disease by administering ERGO PET probes or compositions to a subject in need thereof of a pharmaceutically acceptable dose. In some embodiments, removing the oxidants decreases or prevents the formation of amyloid plaques, thus preventing or slowing the progression of a neurodegenerative disease. Although described herein primarily with respect to neurodegenerative diseases, the disclosure is not so limited and includes other conditions involving oxidants, such as, but not limited to, cancer, cardiovascular disease, and other suitable diseases where antioxidants are beneficial.
Additional details regarding methods of use are provided in Examples 1-3.
The present disclosure provides for ERGO PET probes as well as analogs thereof. The ERGO PET probes or compositions are labeled with a suitable radioisotope, such as, but not limited to, 11C, but optionally substituting H with 18F, 125I, 124I, 131I, 123I, 32Cl, 33Cl, 34Cl, 74Br, 75Br, 76Br, 77Br, 78Br) (e.g., where 11C is not used). In an aspect, the ERGO PET probe is presented by the following structure:
The present disclosure also provides for precursor(s) to the ERGO PET probe(s). In some embodiments, the precursor includes a thiol-histidine molecule with a dimethylamine site available for labeling. For example, in some embodiments, the precursor includes the following structure:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group. In some embodiments, the functional groups of the thiol-histidine molecule, other than the dimethylamine site, are uniformly blocked with acid-labile protecting groups (e.g., tert-Butyloxycarbonyl protecting group (Bop)).
The present disclosure provides for methods of forming the ERGO PET probe. In some embodiments, as illustrated in
In another aspect, the ERGO PET probe is presented by the following structure:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3. TsO− is a tosylate group. In other aspect, the 18F can be substituted with 125I, 124I, 131I, 123I, 32Cl, 33Cl, 34Cl, 74Br, 75Br, 76Br, 77Br, or 78Br.
In another aspect, the present disclosure also provides for precursor(s) to the ERGO PET probe(s). In some embodiments, the precursor includes the following structure:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3.
One method for making the ERGO PET probe including 18F can include the following:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3. R2 can include halogens such as I or Br. Using dimethylamine derivative as a starting material, where the quaternary amine can be generated by an alkylation reaction using either bromo- or iodoalcohol. The resulting alcohol products enable the creation of a tosylate group, which is a great leaving group for [18F] labeling. Since the tosylate salt is a very stable solid, this precursor can be handled and stored with convenience (e.g., in a kit of the present disclosure).
Another method for making the precursor(s) to the ERGO PET probe(s) including 18F is as follows:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3. Another chemical method can be employed for making the tosylate precursor. This work focuses on the alkylation of dimethylamine with di-tosylate derivatives. Since the reaction is very robust, slight heating in anhydrous solvents would suffice (e.g., this precursor can be in a kit of the present disclosure).
For either method of making the precursor above, the following reaction can be used to add the 18F group:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3. For [18F] labeling, the tosylate precursor can be dissolved in an anhydrous and polar aprotic solvent, such as DMF or acetonitrile, before dispensing [18F] fluoride along with potassium carbonate and Kryptofix®222. The temperature of the stirring reaction mixture can be elevated to about 80 to 120° C. for about 20-30 minutes. After labeling, the Boc groups can be removed with trifluoroacetic acid at room temperature in a 5-minute operation to provide the [18F]ERGO PET radioligand.
In another aspect, the present disclosure also provides compounds having the following structure:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3. In other embodiments, F is substituted with Br, I, or Cl.
The following provides for a method of making the compound above:
In an aspect, R1 can be a C1-C4 alkyl group such as a methyl group or butyl group and n is 1, 2, or 3. It may be important to develop “cold” compounds, which will assist with the characterization and purification of the [18F]ERGO PET radioligand. The chemistry for making these compounds can be achieved with the alkylation of dimethylamine starting material with either iodo- or bromofluoromethane or 1-bromo-2-fluoroethane or 1-bromo-3-fluoropropane to afford the corresponding [19F]“cold” compounds.
In general, the ERGO PET probes or compositions can be used in imaging, diagnosing, localizing, monitoring, and/or assessing neurodegenerative disease or inflammatory disease and related biological events as well as tracking response to therapy. Embodiments of the present disclosure can be used to image, detect, study, monitor, evaluate, assess, and/or screen, neurodegenerative disease or inflammatory disease or related biological conditions in vivo or in vitro using the ERGO PET probes or compositions. For example, the ERGO PET probes or compositions provide a detectable signal is emitted that is significantly different from the background signal (e.g., non-inflamed areas) above a certain threshold, indicating the presence of neurodegenerative disease or inflammatory disease, where the threshold depends upon various variables such as the individual subject, the neurodegenerative disease or inflammatory disease, and the like.
In general, the ERGO PET probes or compositions can be used in imaging neurodegenerative disease or inflammatory disease. For example, the ERGO PET probes or compositions is provided or administered to a subject in an amount effective to result in association of ERGO PET probes or compositions with the cells, tissue, or the like associated with the neurodegenerative disease or inflammatory disease. The subject is then introduced to an appropriate imaging system (e.g., PET system) for a certain amount of time (e.g., this depends on radioisotope being used). The ERGO PET probes or compositions becomes associated with cells, tissue, or the like associated with the neurodegenerative disease or inflammatory disease and is detected using the imaging system. The location of the detected signal from the ERGO PET probes or compositions can be correlated with the location of the inflammation associated with the neurodegenerative disease or inflammatory disease. In an embodiment, the dimensions of the location can be determined as well.
In an embodiment, the steps of this method can be repeated at determined intervals so that the location and/or size/stage of the neurodegenerative disease or inflammatory disease can be monitored as a function of time and/or treatment. In particular, the ERGO PET probes or compositions can find use in a subject undergoing treatment (e.g., using a drug, etc.), to aid in visualizing the response of the neurodegenerative disease or inflammatory disease to the treatment. In this embodiment, the ERGO PET probes or compositions is typically visualized and the imaging signal is quantified prior to treatment, and periodically (e.g., daily, weekly, monthly, intervals in between these, and the like) during treatment, and the like, to monitor the regions and extent of the neurodegenerative disease or inflammatory disease.
An embodiment of the present disclosure can include a method for diagnosing the presence of neurodegenerative disease or inflammatory disease that includes: administering to a subject a ERGO PET probes or compositions in a detectably effective amount, wherein the ERGO PET probes or compositions are described herein; imaging at least a portion of the subject; and detecting the ERGO PET probes or compositions, wherein the location of the ERGO PET probes or compositions corresponds to neurodegenerative disease or inflammatory disease corresponding to the neurodegenerative disease or inflammatory disease, where detection of the ERGO PET probes or compositions in a location above a threshold is an indication of presence of the neurodegenerative disease or inflammatory disease at the location.
In an embodiment, the method can be used to select appropriate patients to receive therapy. For example, a patient can be given a selected drug, and the neurodegenerative disease or inflammatory disease can be measured to determine if the drug is having the desired results in the patient.
It should be noted that the amount effective to result in uptake or association of the ERGO PET probes or compositions into the cells or tissue of interest may depend upon a variety of factors, including for example, the age, body weight, general health, sex, and diet of the subject; the time of administration; the route of administration; the rate of excretion of the specific probe employed; the duration of the treatment; the existence of other drugs used in combination or coincidental with the specific composition employed; and like factors, well known in the medical arts.
The present disclosure also provides packaged compositions or pharmaceutical compositions comprising a pharmaceutically acceptable carrier and precursor compounds and/or probes (e.g., precursor compounds for the ERGO PET probes of the disclosure). In certain embodiments, the packaged compositions or pharmaceutical composition includes the reaction precursors and precursor compounds, as provided herein, to be used to generate the ERGO PET probes or compositions according to the present disclosure. Other packaged compositions or pharmaceutical compositions provided by the present disclosure further include materials including at least one of: instructions for making the ERGO PET probes from the precursor compounds, instructions for using the ERGO PET probes or compositions to image a subject, or subject samples (e.g., cells or tissues), which can be used as an indicator of relevant conditions, diseases, and/or biological related conditions as well as other uses described herein.
Embodiments of the present disclosure can be included in one or more of the dosage forms mentioned herein. Unit dosage forms of the pharmaceutical compositions (the “composition” includes at least ERGO PET probes or compositions of the present disclosure) of this disclosure may be suitable for oral, mucosal (e.g., nasal, sublingual, vaginal, buccal, or rectal), parenteral (e.g., intramuscular, subcutaneous, intravenous, intra-arterial, or bolus injection), topical, or transdermal administration to a patient. Examples of dosage forms include, but are not limited to: tablets; caplets; capsules, such as hard gelatin capsules and soft elastic gelatin capsules; cachets; troches; lozenges; dispersions; suppositories; ointments; cataplasms (poultices); pastes; powders; dressings; creams; plasters; solutions; patches; aerosols (e.g., nasal sprays or inhalers); gels; liquid dosage forms suitable for oral or mucosal administration to a patient, including suspensions (e.g., aqueous or non-aqueous liquid suspensions, oil-in-water emulsions, or water-in-oil liquid emulsions), solutions, and elixirs; liquid dosage forms suitable for parenteral administration to a patient; and sterile solids (e.g., crystalline or amorphous solids) that can be reconstituted to provide liquid dosage forms suitable for parenteral administration to a patient.
The composition, shape, and type of dosage forms of the compositions of the disclosure typically vary depending on their use. For example, a parenteral dosage form may contain smaller amounts of the active ingredient than an oral dosage form used to treat the same condition or disorder. These and other ways in which specific dosage forms encompassed by this disclosure vary from one another will be readily apparent to those skilled in the art (See, e.g., Remington's Pharmaceutical Sciences, 18th ed., Mack Publishing, Easton, Pa. (1990)).
Typical compositions and dosage forms of the compositions of the disclosure can include one or more excipients. Suitable excipients are well known to those skilled in the art of pharmacy or pharmaceutics, and non-limiting examples of suitable excipients are provided herein. Whether a particular excipient is suitable for incorporation into a composition or dosage form depends on a variety of factors well known in the art including, but not limited to, the way in which the dosage form will be administered to a patient. For example, oral dosage forms, such as tablets or capsules, may contain excipients not suited for use in parenteral dosage forms. The suitability of a particular excipient may also depend on the specific active ingredients in the dosage form. For example, the decomposition of some active ingredients can be accelerated by some excipients, such as lactose, or by exposure to water. Active ingredients that include primary or secondary amines are particularly susceptible to such accelerated decomposition.
The disclosure encompasses compositions and dosage forms of the compositions of the disclosure that can include one or more compounds that reduce the rate by which an active ingredient will decompose. Such compounds, which are referred to herein as “stabilizers,” include, but are not limited to, antioxidants such as ascorbic acid, pH buffers, or salt buffers. In addition, pharmaceutical compositions or dosage forms of the disclosure may contain one or more solubility modulators, such as sodium chloride, sodium sulfate, sodium or potassium phosphate, or organic acids. An exemplary solubility modulator is tartaric acid.
“Pharmaceutically acceptable salt” refers to those salts that retain the biological effectiveness and properties of the free bases and that are obtained by reaction with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, malic acid, maleic acid, succinic acid, tartaric acid, citric acid, and the like.
Embodiments of the present disclosure include pharmaceutical compositions that include the ERGO PET probes or compositions, pharmaceutically acceptable salts thereof, with other chemical components, such as physiologically acceptable carriers and excipients. One purpose of a pharmaceutical composition is to facilitate administration of the ERGO PET probes or compositions to a subject (e.g., human).
Embodiments of the present disclosure may be salts and these salts are within the scope of the present disclosure. Reference to a compound of any of the formulas herein is understood to include reference to salts thereof, unless otherwise indicated. The term “salt(s)”, as employed herein, denotes acidic and/or basic salts formed with inorganic and/or organic acids and bases. In addition, when an embodiment of the present disclosure contains both a basic moiety and an acidic moiety, zwitterions (“inner salts”) may be formed and are included within the term “salt(s)” as used herein. Pharmaceutically acceptable (e.g., non-toxic, physiologically acceptable) salts are preferred, although other salts are also useful, e.g., in isolation or purification steps which may be employed during preparation. Salts of the compounds of an active compound may be formed, for example, by reacting an active compound with an amount of acid or base, such as an equivalent amount, in a medium such as one in which the salt precipitates or in an aqueous medium followed by lyophilization.
Embodiments of the present disclosure that contain a basic moiety may form salts with a variety of organic and inorganic acids. Exemplary acid addition salts include acetates (such as those formed with acetic acid or trihaloacetic acid, for example, trifluoroacetic acid), adipates, alginates, ascorbates, aspartates, benzoates, benzenesulfonates, bisulfates, borates, butyrates, citrates, camphorates, camphorsulfonates, cyclopentanepropionates, digluconates, dodecylsulfates, ethanesulfonates, fumarates, glucoheptanoates, glycerophosphates, hemisulfates, heptanoates, hexanoates, hydrochlorides (formed with hydrochloric acid), hydrobromides (formed with hydrogen bromide), hydroiodides, 2-hydroxyethanesulfonates, lactates, maleates (formed with maleic acid), methanesulfonates (formed with methanesulfonic acid), 2-naphthalenesulfonates, nicotinates, nitrates, oxalates, pectinates, persulfates, 3-phenylpropionates, phosphates, picrates, pivalates, propionates, salicylates, succinates, sulfates (such as those formed with sulfuric acid), sulfonates (such as those mentioned herein), tartrates, thiocyanates, toluenesulfonates such as tosylates, undecanoates, and the like.
Embodiments of the present disclosure that contain an acidic moiety may form salts with a variety of organic and inorganic bases. Exemplary basic salts include ammonium salts, alkali metal salts such as sodium, lithium, and potassium salts, alkaline earth metal salts such as calcium and magnesium salts, salts with organic bases (for example, organic amines) such as benzathines, dicyclohexylamines, hydrabamines (formed with N,N-bis(dehydroabietyl)ethylenediamine), N-methyl-D-glucamines, N-methyl-D-glucamides, t-butyl amines, and salts with amino acids such as arginine, lysine, and the like.
Basic nitrogen-containing groups may be quaternized with agents such as lower alkyl halides (e.g., methyl, ethyl, propyl, and butyl chlorides, bromides and iodides), dialkyl sulfates (e.g., dimethyl, diethyl, dibutyl, and diamyl sulfates), long chain halides (e.g., decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides), aralkyl halides (e.g., benzyl and phenethyl bromides), and others.
Solvates of the compounds of the disclosure are also contemplated herein. Solvates of the compounds are preferably hydrates.
The amounts and a specific type of active ingredient (e.g., ERGO PET probes or compositions) in a dosage form may differ depending on various factors. It will be understood, however, that the total daily usage of the compositions of the present disclosure will be decided by the attending physician or other attending professional within the scope of sound medical judgment. The specific effective dose level for any particular subject will depend upon a variety of factors, including for example, the activity of the specific composition employed; the specific composition employed; the age, body weight, general health, sex, and diet of the subject; the time of administration; the route of administration; the rate of excretion of the specific compound employed; the duration of the treatment; the existence of other drugs used in combination or coincidental with the specific composition employed; and like factors well known in the medical arts. For example, it is well within the skill of the art to start doses of the composition at levels lower than those required to achieve the desired effect and to gradually increase the dosage until the desired effect is achieved.
The presently-disclosed subject matter is further illustrated by the following specific but non-limiting examples. The following examples may include compilations of data that are representative of data gathered at various times during the course of development and experimentation related to the presently-disclosed subject matter.
This Example discusses the development and validation of Ergothioneine (ERGO) PET radioligands. ERGO is a rare amino acid mostly found in fungi, including mushrooms, with recognized antioxidant activity to protect tissues from damage by reactive oxygen species (ROS) components. The biodistribution of ERGO has previously been performed solely in vitro using extracted tissues. This Example discusses the development of a feasible chemistry for the synthesis of an ERGO PET radioligand, [11C]ERGO, to facilitate in vivo study. The radioligand probe was synthesized with identical structure to ERGO by employing an orthogonal protection/deprotection approach. [11C]methylation of the precursor was performed via [11C]CH3OTf to provide [11C]ERGO radioligand. The [11C]ERGO was isolated by RP-HPLC with a molar activity of 690 TBq/mmol.
To demonstrate the biodistribution of the radioligand, approximately 37 MBq/0.1 mL was administered in 5XFAD mice, a mouse model of Alzheimer's disease, via the tail vein. The distribution of ERGO in the brain was monitored using 90-minute dynamic PET scans. The delivery and specific retention of [11C]ERGO in an LPS-mediated neuroinflammation mouse model was also demonstrated. For the pharmacokinetic study, the concentration of the compound in the serum started to decrease 10 min after injection while starting to distribute in other peripheral tissues. In particular, a significant amount of the compound was found in the eyes and small intestine. The radioligand was also distributed in several regions of the brain of 5XFAD mice, and the signal remained strong 30 min post-injection. This is the first time the biodistribution of this antioxidant and rare amino acid has been demonstrated in a preclinical mouse model in a highly sensitive and non-invasive manner.
L-ergothioneine (ERGO) is a food-derived hydrophilic antioxidant available in fungi and various bacteria, but not in animals or higher plants. It has been known as an antioxidant since its discovery a century ago from fungi of the genus Claviceps purpurea. Chemically, this rare betaine-based amino acid has a similar chemical structure to histidine but with the presence of a sulfhydryl moiety on the imidazole ring. The molecule exists as a tautomeric form between thioketone and thiol derivatives (
ERGO is also implicated in a number of neurological pathways. Substantial research data indicate that ERGO is a physiological antioxidant cytoprotectant. Protection against cytotoxicity elicited by Cu (II), hydrogen peroxide, iron, and sodium nitrite is derived from the conspicuous affinity of ERGO for metal cations, such as Fe and Cu, permitting capture and neutralization of associated radicals. It has been demonstrated that ERGO concentration decreases significantly with age, and markedly lower levels were found in individuals with mild cognitive impairment compared to the controls, supporting the potential for ERGO deficiency to act as a risk factor for neurodegeneration. It is worthwhile to mention that ERGO does not permeate the blood-brain barrier (BBB); its uptake in cells is mediated by an OCTN1 (organic cation transporter novel, type 1) receptor. Other studies have shown that ERGO can protect neurons both in vitro and in vivo against a spectrum of stressors. Taken altogether, these data strongly suggest that ERGO is involved in healthy aging, serving as a “longevity vitamin”. The term “vitamin” is used in here since ERGO is a micronutrient, that the body does not need a lot of to function, but the material needs to be constantly available by uptake from an external source such as foods or supplements and it therefore does fit into that category.
To date, all preclinical studies had relied solely on in vitro analysis of ERGO using analytical and bioassay methods for analyzing the ERGO distribution from extracted tissues. The same holds true for clinical studies to validate the benefit of ERGO consumption in the diet; serum samples were collected for assessing the ERGO levels. This necessitated the development of an ERGO probe to facilitate non-invasive, real-time, and repeated imaging of ERGO distribution and pharmacokinetics in preclinical and clinical settings. To this end, report herein for the first time is the development of a [11C]ERGO radioligand. Further, this Example demonstrates that this antioxidant could be distributed and retained in the brain of a mouse model of Alzheimer's disease. This observation was further confirmed using a mouse model of LPS-induced neuroinflammation. The proof-of-principle PET imaging in this Example showed that ERGO is distributed across several subregions in the brains, albeit with much higher retention in pathological brains than normal counterparts. Interestingly, the whole-body biodistribution study showed that ERGO is also distributed significantly in the eyes and small intestine.
TEMPOL was acquired from Tocris Bioscience (Fisher Scientific). Animal experiments were conducted per the guidelines established by the Vanderbilt University's Institutional Animal Care and Use Committee (IACUC) and the Division of Animal Care. The performed work was approved by Vanderbilt IACUC with an extended protocol, M1700044-01. In addition, all of the works involving live animals were compliant with the ARRIVE guidelines. In a typical imaging procedure, anesthetized mice received 2% of isoflurane via inhalation, supplied with oxygen using a precision vaporizer.
All commercially available reagents and solvents were used as received. L-(+)-Ergothionene was purchased from Cayman Chemicals. Reactions were monitored by a Agilent LC/MS 1260 Infinity II. Products were purified using a Telodyne Combiflash Rf automated purification instrument using normal phase or reverse phase. NMR spectra were recorded on a 400 MHz Bruker AVANCE 400 equipped with a 9.3 T Oxford Magnet or 600 MHz Bruker AVIII console equipped with a 14.1 T Bruker Magnet. 1H NMR chemical shifts were referenced to the residual solvent signal; 13C NMR chemical shifts were referenced to the deuterated solvent signal. Data are presented as follows: chemical shift d (ppm), multiplicity (s=singlet, d=doublet, dd=doublet of doublet, t=triplet, m=multiplet).
1. NT-M9H-fluoren-9-yl)methoxy)carbonyl)-Nα-(tert-butoxycarbonyl)-L-histidine 2. To a stirring solution of histidine amino acid 1 (1.0 g, 3.9 mmol), FMOC-succinimide (1.45 g, 4.3 mmol), and DIPEA (0.605 g, 4.7 mmol) in methylene chloride (50 mL) and stirred overnight. Reaction was diluted with water and methylene chloride. The product was extracted 3× with methylene chloride. The organic layers were combined, washed with 1M HCl, saturated sodium bicarbonate, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide a desired product with 60% yield.
1H CDCl3 (400.13 mHz): 8.26 (d, J=1.2 Hz, 1H); 7.79 (d, J=7.6 Hz, 2H); 7.56 (d, J=7.6 Hz, 2H); 7.43, (t, J=7.2 Hz, 2H); 7.34 (t, J=7.2 Hz, 2H); 7.24 (s, 1H); 5.51 (d, J=6.0 Hz, 1H); 4.70 (dd, J1=7.2 Hz, J2=1.6 Hz, 2H); 4.56 (t, J=7.6 Hz, 1H); 4.35 (t, J=6.8 Hz, 1H); 3.32 (dd, J1=14.8 Hz, J2=2.8 Hz, 1H); 3.20 (dd, J1=14.4 Hz, J2=5.2 Hz, 1H); 1.47 (s, 9H). 13C CDCl3 (100.6 mHz): 172.9, 168.6, 155.4, 148.1, 142.7, 141.5, 137.5, 128.4, 127.6, 124.9, 120.5, 115.6, 80.0, 70.6, 53.6, 52.8, 46.6, 29.9, 28.5.
2. (9H-fluoren-9-yl)methyl(S)-4-(3-(tert-butoxy)-2-((tert-butoxycarbonyl)amino)-3-oxopropyl)-1H-imidazole-1-carboxylate 3. To a stirring solution of 2 (3.90 mmol) in methylene chloride (50 mL) and tert-butanol (10 mL) at 0 C was added: EDC-HCl (744 mg, 3.9 mmol), and DMAP (95 mg, 0.78 mmol. This solution was allowed to warm up to r.t. and stirred overnight. Reaction was diluted with water and methylene chloride. The product was extracted 3× with methylene chloride. The organic layers were combined, washed with 1M HCl, saturated sodium bicarbonate, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide the desired product (12% yield).
1H CDCl3 (400.13 mHz): 7.99 (s, 1H); 7.81 (d, J=7.6 Hz, 2H); 7.58 (d, J=7.6 Hz, 2H); 7.48, (t, J=7.2 Hz, 2H); 7.35 (t, J=7.2 Hz, 2H); 7.17 (s, 1H); 5.03 (m, 1H); 4.72 (dd, J1=6.4 Hz, J2=2.0 Hz, 2H); 4.20 (m, 1H); 3.03 (m, 2H); 1.44 (s, 9H).
3. (9H-fluoren-9-yl)methyl (S)-4-(2-amino-3-(tert-butoxy)-3-oxopropyl)-1H-imidazole-1-carboxylate 4. To a stirring solution of 3 (3.90 mmol) in methylene chloride at −78° C. was added TFA (5 mL) dropwise. This solution was allowed to warm up to 0° C. and stirred until completion. The solution was then neutralized with sodium bicarbonate and diluted with water and methylene chloride. The product was extracted 3× with methylene chloride. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide the desired product with 63% yield.
1H CDCl3 (400.13 mHz): 7.99 (s, 1H); 7.77 (d, J=7.6 Hz, 2H); 7.57 (d, J=6.8 Hz, 2H); 7.41, (t, J=6.0 Hz, 2H); 7.33 (t, J=7.6 Hz, 2H); 7.14 (s, 1H); 5.03 (m, 1H); 4.59 (m, 2H); 4.18 (m, 1H); 3.05 (m, 2H); 1.38 (s, 9H).
4. tert-butyl NαNα-dimethyl-L-histidinate 5. To a stirring solution of 4 in MeOH (20 mL) was added NaBH3CN (362 mg, 5.8 mmol) and CH2O (37% in H2O, 702 mg, 23.4 mmol). The reaction was capped and stirred for 2 hrs. The resulting solution was then concentrated via rotovap. The crude oil was purified by reverse phase chromatography. The product was verified by LC/MS and used as is in the next step with a 82% yield. The Fmoc group was removed in this step through interaction with the NaBH3CN to provide the desired product.
1H D20 (400.13 mHz): 7.47 (s, 1H); 6.83 (s, 1H); 4.79 (m, 1H); 4.29 (m, 2H); 2.58 (s, 6H); 1.24 (s, 9H).
5. tert-butyl (S)-2-(dimethylamino)-3-(2-thioxo-2,3-dihydro-1H-imidazol-4-yl)propanoate 6. To a stirring solution of 5 (31.5 mg, 0.13 mmol) in water (2 mL) and diethyl ether (2 mL) was added sodium bicarbonate (65 mg, 0.78 mmol), and phenylchloro thionoformate (24.7 mg, 0.14 mmol) and stirred overnight. Reaction was diluted with water and diethyl ether. The product was extracted 3× with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The resulting oil was then redissolved in MeOH (5 mL) and triethylamine (55 uL) was added. This solution was stirred overnight. The resulting solution was then concentrated under reduced pressure. Product was purified by reverse phase chromatography to provide a final product (16.0 mg) 45% yield. And the product was immediately used for the next step.
6. tert-butyl (S)-4-(3-(tert-butoxy)-2-(dimethylamino)-3-oxopropyl)-2-((tert-butoxycarbonyl)thio)-1H-imidazole-1-carboxylate 7. To a stirring solution of 6 (16.0 mg, 0.066 mmol) in methylene chloride (10 mL) was added: Boc anhydride (32 mg, 0.145 mmol), and DIPEA (19 mg, 0.145 mmol) and stirred over the course of 48 h. The resulting solution was concentrated and purified by flash chromatography (0-50% CH2Cl2/(20% MeOH/CH2Cl2)) to afford the precursor 7 (15.0 mg) with 48% yield.
1H CDCl3 (600.13 mHz): 7.16 (s, 1H); 3.40 (m, 1H); 2.86 (dd, J1=14.4 Hz, J2=8.4 Hz, 1H); 2.72 (dd, J1=14.4 Hz, J2=6.6 Hz, 1H); 2.28 (s, 6H); 1.48 (s, 9H); 1.37 (s, 9H); 1.32 (s, 9H). 13C CDCl3 (150.9 mHz): 170.9, 165.3, 146.7, 139.9, 135.1, 119.8, 86.8, 85.8, 81.2, 67.3, 41.8, 29.8, 28.6, 28.3, 28.2, 27.9, 22.3, 22.0.
MS: calculated: 471.2403, detected: 471.1845.
The [11C]CO2 was made by irradiating a target filled with nitrogen and 1% oxygen gas with protons. The [11C]CO2 was then trapped on nickel Shimalite with molecular sieves at room temperature. The [11C]CO2 was then converted to [11C]CH4 by heating the trapped [11C]CO2 to 400° C. in the presence of hydrogen gas. The [11C]CH4 was then released from the nickel Shimalite at 400° C. and isolated on molecular sieves at −75° C. The [11C]CH4 was then converted to [11C]MeI via a recirculation through gaseous iodine at ˜720° C., with the [11C]MeI being trapped on Porapak N with each cycle. The [11C]MeI was then released from the Porapak N by heating with a gentle flow of helium that is passed through an AgOTf impregnated column at ˜200° C. to convert the [11C]MeI to [11C]MeOTf. This [11C]MeOTf was bubbled into a solution of precursor in 250 μl acetonitrile at −10° C. After the activity transfer was complete, the reaction mixture was heated to 80° C. for 2 minutes. At this time, hydrochloric acid (6M, 250 μl) was added, and the reaction mixture was heated at 70° C. for 5 minutes, cooled to room temperature, and diluted with water (1 mL). The reaction mixture was passed through an ion-retardation resin (Ag11-A8, 3 g) into the product vial, and the resin was rinsed with water (5 mL) into the product vial. The product was then transferred to the final vial, and an aliquot was removed for quality control analysis.
The radiochemical purity and the identity of the [11C]ERGO were characterized using an analytical HPLC system, equipped with a UV absorption detector (λ=254 nm) and a radio-detector (Bioscan Flow-Count). The chromatography setup included a SeQuant ZIC-HILIC 150×4.6 mm with a typical mobile phase of acetonitrile (75%) in water at a flow rate of 1 mL/min. The identity of the [11C]ERGO was confirmed by comparing the retention time with co-injected and unlabeled ERGO along with the gamma peak. The molar activity of the radioligand is 690 TBq/mmol.
The dynamic acquisition was divided into twelve 5 sec frames, four 60 sec frames, five 120 sec frames, three 5 min frames, and six 10 min scans. The data from all possible lines of response (LOR) were saved in the list mode raw data format. The raw data were then binned into 3D sinograms with a span of 3 and ring difference of 47. The images were reconstructed into transaxial slices (128×128×159) with voxel sizes of 0.0815×0.0815×0.0796 cm3, using the MAP algorithm with 16 subsets, 4 iterations, and a beta of 0.0468. For anatomical co-registration, immediately following the PET scans, the mice received a CT scan in a NanoSPECT/CT (Mediso, Wash. D.C.) at an X-ray beam intensity of 90 mAs and x-ray peak voltage of 45 kVp. The CT images were reconstructed into 170×170×186 voxels at a voxel size of 0.4×0.4×0.4 mm3. The PET/CT images were uploaded into Amide software (www.sourceforge.com), co-registered to an MRI template made in-house, and volumetric regions-of-interest were drawn around the cortex, hippocampus, striatum, thalamus, and cerebellum in addition to the whole brain. The PET images were normalized to the injected dose, and the time-activity-curves (TACs) of the mean activity within the ROIs were estimated for the entire duration of the scans.
The mice were injected with ˜20 MBq/0.1 ml 11C-ERGO via the tail vein and returned to their cages for 10 min. Then they were anesthetized with 2% isofluorane and imaged in an Inveon microPET (Siemens Pre-clinical, Knoxville, Tenn., USA) for 30 min in static mode followed by a CT scan using a NanoSPECT/CT (Mediso, Wash. D.C.) at an x-ray beam intensity of 90 ms and x-ray voltage of 45 kVp. PET images were reconstructed using the iterative MAP reconstruction algorithm with 18 iterations and a beta smoothing value of 0.001 into 128×128×95 slices with a voxel size of 0.388 mm×0.388 mm×0.796 mm. The CT images were reconstructed into 170×170×126 slices at a voxel size of 0.4×0.4×0.4 mm{circumflex over ( )}3. The PET and CT images were co-registered using the imaging tool AMIDE.
At 5 or 10 min post injection, anesthetized mice were laid on the shallow tray filled with crushed ice and the thoracic cavity was accessed using a scalpel after making 5-6 cm mid-line incision from the abdominal area. After careful separation of the liver from the diaphragm, the thoracic opening was stabilized with a retractor. Perfusion was performed as we described in the past. Following removal of air bubbles, approximately 30 mL (pH7.4) of ice-cold PBS buffer is slowly injected in the left ventricle toward the ascending aorta using a 25-G syringe while the right atrium was snipped off using a curved point squeeze snip scissors to facilitate drainage of the systemic venous return. Then, 30 mL of 4% paraformaldehyde (PFA, pH 7.4) was perfused. When completed, tissues were harvested and weighed before counting using the automatic gamma counter (Hidex).
5XFAD and control C57BL/6J mice were maintained at Vanderbilt University under standard conditions, in a 12-h light/dark cycle, and with free access to food and water. The 5XFAD mice over express both mutant human amyloid precursor protein (APP) and presenilin 1 (PS1), correlating with high burden and accelerated accumulation of the A13. A colony of 5XFAD transgenic mice obtained from Jackson Laboratories was maintained by crossing 5XFAD mice with a WT C57BL/6J strain. The 5XFAD mice were maintained as heterozygous.
The mouse model of LPS-induced neuroinflammation was developed based on past reports. The LPS derived from Escherichia coli 0111:64 (Sigma Aldrich, St Louis, Mo.) was formulated in sterilized dd. water and given a high dose of LPS formulation (5 mg/Kg) through intraperitoneal injection 24 h before PET imaging. This high dose would result in approximately 12-13% body weight loss over the course of 24 h. After PET imaging, animals were sacrificed, and the brains were collected for histology analysis.
Brains embedded in OCT were cut into sagittal sections (10 μm) using a Tissue-Tek cryostat and mounted onto charged glass slides. Prior to staining, slides were washed with PBS (10 min); then, they were treated with blocking buffer (5% normal goat serum, 0.2% Triton X-100, 0.5% bovine albumin in PBS) for 1 h at room temperature. The treated sections were then incubated overnight at 4° C. with primary anti-GFAP antibody (1:100 dilution, Biolegend San Diego, Calif., USA). Slides were washed with PBS (3×) for 10 min each, the sections were subsequently incubated with secondary antibody goat anti-mouse Alexa Fluor 488 (1:200 dilution, Thermo Fisher Scientific, Carlsbad, Calif., USA) for 30 min at room temperature. The sections were then washed with PBS twice for 10 minutes and once for 30 minutes, and cover slipped with an antifade mounting medium (Vector Laboratories, Burlingame, Calif.) before observation under a fluorescence microscope.
Unpaired t-test was used to compare the mean signal (% ID/g) difference between two independent subjects. A P value of ≤0.05 was considered as a statistically significant difference.
Retrosynthetic analysis of [11C]CH3 labeled ERGO suggests the precursor should have the thiol-histidine molecule with the dimethylamine site available for labeling, while the rest of other functional groups should be uniformly blocked with acid-labile protection groups (
With the precursor available, next, we labeled the ERGO precursor 7 with [11C]CH3 using a commercial automated radiosynthesis module (GE TRACERlab FXc-Pro). The [11C]CO2 was converted to [11C]MeOTf using the standard reaction conditions, reacted with precursor 7 at 80° C., and subsequently deprotected under acidic conditions to yield [11C]ERGO 8 (Supplementary data,
To test the distribution of ERGO non-invasively in vivo, approximately 37 MBq/0.1 mL of [11C]ERGO probe was given to anesthetized 5XFAD mice (8-month-old, n=4) in single bolus intravenous (I.V.) injection via the lateral tail vein. The administration of the probe was simultaneous with the start of a 90-minute dynamic PET imaging, followed by subsequent CT scan. The PET images were normalized to the injected dose, and the time-activity-curves (TACs) of the mean activity within the ROIs were estimated for the entire duration of the scans. Within 5 min post I.V. injection, [11C]ERGO can be detected in the brain parenchyma (
The reported LPS mouse model of neuroinflammation in the past [40] was reproduced for the validation of the specificity of the probe. Approximately 24 h after injection of WT mouse with LPS (5 mg/Kg) via intraperitoneal injection, the animals showed signs of withdrawing and lacked grooming. The animals experienced noted body weight loss over 10% within a day after treatment. Further, histological analysis of the brain sections at the hippocampal region showed a significant upregulation of GFAP in the LPS-treated mice (
Cohorts of WT mice were injected with [11C]ERGO probe, followed by cardiac perfusion 5 (n=5), 10 (n=5) and 30 (n=6) minutes after injection before tissues were collected for activity counting. The data in
One of the objectives of this probe development was to assess a number of synthetic pathways to ensure the probe would be designed in a way that minimized the potential alternation of the intrinsic chemical structure. Ideally, we sought to maintain an identical structure to ERGO. In this respect, the most logical approach focuses on the quaternary amine, which presents a convenient opportunity to insert the [11C]CH3 radioisotope through the use of an [11C]CH3 electrophile. Since ERGO comprises four distinct functional groups and each can be activated as a strong nucleophile at their respective pKa, so it is conceivable that each step of the chemistry may require prior protection and deprotection using orthogonal strategy. Further, incorporating these protecting groups is crucial to enhance the hydrophobicity of this water-soluble zwitterion molecule for organic solvents. Given that ERGO and histidine share an overall structural similarity; therefore, taking all of these observations into an account, the design suggests the adoption of either N- or C-terminal protected histidine as the starting material.
Multiple attempts were tried to synthesize the precursor 7; in almost every attempt, two major issues were encountered. First, the product was so polarized that it proved to be challenging for purification using flash chromatography. Second, the protecting groups were sometimes so bulky that they obscured the next step in the process, or they were cleaved off. Therefore, a protecting group must be carefully selected for the successful synthesis. As in this case, using an orthogonal strategy, the Fmoc group can be removed without affecting the Boc group in the following steps. Aside from protection, the Fmoc helps to enhance hydrophobicity and its UV active nature, enables reaction monitoring. After three functional groups were protected, the Boc from the N-terminal region was selectively removed using TFA in methylene chloride at −78° C. to afford 4 (
ERGO has multiple advantages when it comes to studying oxidative stress in the brain, given the molecule is very water soluble, ideal for the clinical formulation whether it is for I.V. injection or for oral usage. But the paradox is that hydrophilic molecules cannot cross the blood-brain barrier (BBB). A unique feature of ERGO compared to other antioxidants is that its distribution to the brain parenchyma is independent of the BBB, but rather mediated by OCTN1 receptors. In clinical trials, either pure ERGO or mushrooms have been given to testing subjects for examining its effect on biomarkers of oxidative damage and inflammation. So far, all ERGO biodistribution and pharmacokinetics analysis rely on the indirect analysis of blood and urine samples.
The availability of the probe enables dynamic imaging to assess the biodistribution and kinetics of ERGO at any target of interest. Further, it also provides information for mapping OCTN1 receptors. For instance, the data in
The retention of the [11C]ERGO probe depicted by strong signal in the brains of 5XFAD mice during PET scans (
Similar to the brain study, data from the whole-body biodistribution showed that 5 minutes post-injection, ERGO started to present in the peripheral tissues, as the levels in the blood reduced significantly (
Different from the in vivo PET imaging information, the biodistribution data showed that over the thirty minutes after administration, the ERGO continues to accumulate in most of the tissues, including the brain (
In summary, a new [11C]ERGO PET radioligand has been synthesized to facilitate in vivo, non-invasive and real-time imaging of the biodistribution of ERGO. The development of a probe with an identical structure of ERGO is a significant advantage to our design. As such, all pharmacokinetics and biodistribution shown in this work are expected to reflect those of native compounds. Further, the availability of the PET radioligand enables the performance of longitudinal investigations in the same animals. Thus, differences between animals due to inter-individual variations can be controlled for. Overall, we anticipate that this probe will pave the way for the integration of molecular imaging with food biomarkers and biomedical research. The probe provides an emerging capability that will benefit the ERGO research community.
Transporter. Drug Metab Dispos. 2018; 46:779-85. doi:10.1124/dmd.118.080440.
L-ergothioneine (ERGO) is a potent antioxidant synthesized by actinomycetes, cyanobacteria, methylbacteria, and some fungi, like mushrooms [1]. It has been reported that ERGO can prevent cell and tissue damage, a key contributor to aging, by protecting against free radicals and oxidative stress [2-4]. The chemical structure of ERGO is similar to that of histidine but with the presence of a thione group on the imidazole ring [5]. It is reported that ERGO protects against cytotoxicity by scavenging singlet oxygen, hydroxyl radicals [6-8], hypochlorous acid (HOCl), peroxyl radicals [8, 9], and acting as an inhibitor of iron or copper ion-dependent generation of hydroxyl radicals from hydrogen peroxide [6]. This protection is derived from its conspicuous affinity for metal cations, such as Fe and Cu, permitting capture and neutralization of associated radicals [10]. Thus, ERGO is considered a potent antioxidant with potential therapeutic implications. In particular, this antioxidant might play essential roles in the central nervous system [11-13], given the substantial research data indicating that ERGO can be distributed to the brain via the OCTN1 transporter [10].
Our group recently reported the synthesis of an [11C]ERGO PET radioligand to facilitate in vivo imaging of the biodistribution and pharmacokinetics using preclinical mouse models [5]. The work also demonstrated the specificity of the probe for the detection of LPS-induced inflammation and oxidative stress. In the previous synthesis, the carboxylic group of histidine was protected as a t-butyl ester for the synthesis of the precursor. After labeling with a [11C]CH3 positron emitter, all of the acidic-labile protecting groups, including the t-butyl ester, were cleaved by treating with hydrochloric acid at 80° C. The advantage of using t-butyl ester is its sensitivity to an acidic condition, albeit with sufficient stability to survive very mild acidic conditions at low temperature. This feature serves best when robust deprotection conditions are required. The t-butyl ester's strength, however, is also its shortcoming. Its sensitivity in an acidic condition made reaction workup harder than usual, and thus, low reaction yield is inevitable.
The issue mentioned above is further compounded by the reproducibility problem pertaining to the presence of the t-butyl ester. To overcome these drawbacks, we switched the t-butyl ester group to a more stable methyl ester counterpart, although this new chemistry needs one additional step during radioisotope labeling. The reproducibility of this design is the real impetus behind this work. This article describes an improved synthesis with an overall yield of 24% starting from the methyl ester to the precursor, compared to 14% as reported in the past [5].
Given the apparent implications of reactive oxygen species (ROS) in mitochondrial dysfunction related to the pathogenesis of AD [14], we used the resultant [11C]ERGO PET radioligand to test the incipient hypothesis that oxidative stress could potentially serve as a biomarker for AD [15-18]. Here, we present the data demonstrating that the probe can detect oxidative stress in the brains of a common mouse model for Alzheimer's disease (AD) neuropathology 5XFAD mice. The in vivo PET imaging showed the probe was retained in the brain of 5XFAD mice with a higher concentration than wild-type (WT) counterparts. As expected, this is due to the trapping of the probe, given its high affinity for ROS products and oxidized metals associated with AD [19-23]. Overall, the [11C]ERGO PET radioligand enables us to observe, for the first time, the dynamics of this antioxidant in action noninvasively in a live subject.
Development of a precursor. The carboxylic group of protected histidine 1 was capped as a methyl ester by a routine procedure using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) with a trace 4-dimethylaminopyridine (DMAP) as a catalyst in methanolic dichloromethane (
Radiosynthesis of [11C]ERGO PET radioligand. Direct methylation of precursor 6 was achieved using [11C]MeOTf in acetonitrile (ACN) (
Dynamic uptake and retention of [11C]ERGO radioligand. Two cohorts of age-matched mice (10-month-old, n=4, each), including 5XFAD and WT animals, were injected with a consistent amount of 14.8 MBq of [11C]ERGO in 0.1 mL via the tail vein prior to acquiring dynamic imaging. Our previous PET imaging data indicated that ERGO started to present in the brain 5 min post-injection, and it continued to accumulate until 30 min before saturation [5]. In this work, we decided to run 20-min dynamic scans to test, as a proof-of-concept, whether the affinity of ERGO for radicals and/or metals, which are integrated in or very closely associated with Abeta aggregates [24-29], would trap the probe. As shown in a representative set of dynamic scans along with the corresponding time-activity curves (TAC) (
All solvents and chemicals were purchased from common vendors at reagent grade and were used without further purifications. 1H- and 13C-NMR spectra were obtained using a Bruker 600-MHz NMR spectrometer equipped with cryogenic radio frequency probe.
Compound 2. To a stirring solution of 1 (535 mg, 1.12 mmol) in CH2Cl2 (10 mL) and methanol (5 mL) at 0° C. was added with EDC-HCl (257 mg, 1.3 mmol), and DMAP (25 mg, 0.22 mmol. This solution was allowed to warm up to room temperature (r.t.) and stirred overnight. The reaction was diluted with H2O and CH2Cl2. The product was extracted 3× with CH2Cl2. The organic layers were combined, washed with 1M HCl, saturated sodium bicarbonate, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. Purified by flash chromatography (0-50% CH2Cl2/(20% MeOH/CH2Cl2)), (241 mg, 45% yield). 1H CDCl3 (600.13 mHz): 7.97 (d, J=0.6 Hz, 1H); 7.80 (d, J=7.2 Hz, 2H); 7.57 (d, J=7.8 Hz, 2H); 7.44, (t, J=7.2 Hz, 2H); 7.35 (t, J=7.8 Hz, 2H); 7.16 (s, 1H); 5.66 (d, J=7.8 Hz, 1H); 4.72 (d, J1=6.6 Hz, 2H); 4.60 (m, 1H); 4.35 (t, J=6.6 Hz, 1H); 3.72 (s, 3H); 3.09 (dd, J1=15.0 Hz, J2=5.4 Hz, 1H); 3.04 (dd, J1=15.0 Hz, J2=4.8 Hz, 1H); 1.44 (s, 9H). 13C CDCl3 (150.9 mHz): 172.3, 155.6, 148.5, 142.8, 141.5, 139.5, 137.0, 128.4, 127.6, 124.9, 120.5, 114.6, 80.0, 69.9, 53.2, 52.5, 46.7, 30.4, 28.5.
Compound 3. To a stirring solution of 2 (241 mg, 0.50 mmol) in CH2Cl2 (20 mL) at −78° C. was added TFA (2 mL) dropwise. This solution was allowed to warm up to 0° C. and stirred until completion. The solution was then neutralized with sodium bicarbonate and diluted with H2O and CH2Cl2. The product was extracted 3× with CH2Cl2. The organic layers were combined, washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The product was purified by flash chromatography (0-50% CH2Cl2/(20% MeOH/CH2Cl2)), (172 mg, 88% yield). 1H CDCl3 (600.13 mHz): 8.24 (s, 1H); 7.79 (d, J=7.2 Hz, 2H); 7.54 (d, J=7.8 Hz, 2H); 7.43, (t, J=7.2 Hz, 2H); 7.40, (s, 1H); 7.33 (t, J=7.2 Hz, 2H); 4.78 (dd, J1=6.6 Hz, J2=1.8 Hz, 2H); 4.43 (br.s, 1H); 4.35 (t, J=6.6 Hz, 1H); 3.79 (s, 3H); 3.38 (d, J=13.8 Hz, 1H); 3.30 (dd, J1=15.6 Hz, J2=6.6 Hz, 1H). 13C CDCl3 (150.9 mHz): 168.4, 147.3, 142.4, 141.5, 136.9, 134.8, 128.5, 127.6, 124.8, 120.5, 116.6, 71.1, 53.8, 52.9, 46.6, 26.4.
Compound 4. To a stirring solution of 3 (172 mg, 0.44 mmol) in MeOH (10 mL) was added NaBH3CN (63 mg, 1.0 mmol) and CH2O (37% in H20, 90 mg, 3.0 mmol). The reaction was capped and stirred overnight. The resulting solution was then concentrated via rotovap. Purified by reverse phase flash chromatography (0-50% H2O/ACN), (68 mg, 79% yield). The FMOC group was removed in this step through interaction with the NaBH3CN. 1H CDCl3 (400.13 mHz): 7.47 (s, 1H); 6.75 (s, 1H); 3.61 (s, 3H); 3.48 (t, J=7.6 Hz, 1H); 3.01 (dd, J1=14.8 Hz, J2=8.0 Hz, 1H); 2.88 (dd, J1=14.8 Hz, J2=6.8 Hz, 1H); 2.33 (s, 6H). 13C CDCl3 (100.6 mHz): 172.0, 134.8, 133.1, 118.5, 67.6, 51.3, 41.7, 26.5.
Compound 5. To a stirring solution of 4 (68 mg, 0.34 mmol) in H2O (2 mL) and diethyl ether (2 mL) was added NaHCO3 (211 mg, 2.5 mmol), and phenyl chlorothionoformate (158 mg, 0.42 mmol) and stirred overnight. Reaction was diluted with H2O and diethyl ether. The product was extracted 3× with diethyl ether. The organic layers were combined, washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting oil was then redissolved in MeOH (5 mL) and triethylamine (174 μL) was added. This solution was stirred overnight. The resulting solution was then concentrated under reduced pressure. The final product was purified by flash chromatography (0-50% CH2Cl2/(20% MeOH/CH2Cl2)), (50 mg, 64% yield).
Compound 6. To a stirring solution of 5 (50 mg, 0.218 mmol) in CH2Cl2 (6 mL) was added: Boc anhydride (190 mg, 0.873 mmol), and DIPEA (113 mg, 0.873 mmol) was heated to 37° C. overnight. The reaction was cooled to r.t. and diluted with CH2Cl2 and H2O. The product was extracted 3× with CH2Cl2. The organic layers were combined, washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. Purified by flash chromatography (0-50% CH2Cl2/(20% MeOH/CH2Cl2)), (50 mg, 54% yield). 1H CDCl3 (400.13 mHz): 7.36 (s, 1H); 3.65 (s, 3H); 3.63 (m, 1H); 2.88 (dd, J1=14.4 Hz, J2=8.4 Hz, 1H); 2.86 (dd, J1=14.4 Hz, J2=6.0 Hz, 1H); 2.35 (s, 6H); 1.58 (s, 9H), 1.46 (s, 9H). 13C CDCl3 (100.6 mHz): 171.9, 165.3, 146.7, 139.7, 135.2, 119.8, 86.8, 85.9, 66.7, 51.3, 41.8, 29.8, 28.2, 27.9.
The [11C]ERGO radioligand was prepared using the GE Healthcare Tracerlab FXC-Pro, a commercially supplied reaction platform, modified to directly connect V7nc to V11no. The [11C]CO2 is made by irradiating a target filled with nitrogen and 1% oxygen gas with protons. The [11C]CO2 is then trapped on nickel Shimalite with molecular sieves at room temperature. The [11C]CO2 is then converted to [11C]CH4 by heating the trapped [11C]CO2 to 400° C. in the presence of hydrogen gas. The [11C]CH4 is then released from the nickel Shimalite at 400° C. and isolated on molecular sieves at −75° C. The [11C]CH4 is then converted to [11C]MeI via a recirculation through gaseous iodine at ˜720° C., with the [11C]MeI being trapped on Porapak N with each cycle. The [11C]MeI is then released from the Porapak N by heating with a gentle flow of helium that is passed through an AgOTf impregnated column at ˜200° C. to convert the [11C]MeI to [11C]MeOTf; this [11C]MeOTf is bubbled into a solution of precursor in 250 μI acetonitrile at −10° C. After the activity transfer is complete the reaction mixture was heated to 80° C. for 2 minutes. At this time trifluoroacetic acid (250 μl) was added, the reaction mixture heated at 70° C. for 3 minutes, 5M of aqueous NaOH (1 mL) added and heated at 70° C. for 4 minutes. The reaction mixture was cooled to room temperature, passed through an ion-retardation resin (Ag11-A8, 3 g) into the product vial and the resin was rinsed with water (5 mL) into the final product vial.
We labeled the precursor 6 with [11C]CH3OTf using a commercial automated radiosynthesis module (GE TRACERlab FXc Pro). [11C]CO2 was converted to [11C]MeOTf using the standard reaction conditions, reacted with precursor 6 at 80° C. to give the protected intermediate. The Boc-groups were removed under acidic conditions followed by the use of 5M aqueous sodium hydroxide both to neutralize the TFA, and for the saponification of the methyl ester to provide an [11C]ERGO radioligand. The [11C]ERGO was passed through an ion-retardation resin, the pH was adjusted with aqueous HCl before use.
All animal experiments performed complied with institutional guidelines and were conducted according to the protocol approved by the Vanderbilt Institutional Animal Care and Use Committee. The 5XFAD mice were maintained at Vanderbilt University under standard conditions, in a 12-h light/dark cycle and with free access to food and water. The 5XFAD mice over express both mutant human APP and PS1 genes and it correlates with high APP levels correlating with high burden and accelerated accumulation of β-amyloid (Abeta). A colony of 5XFAD transgenic mice obtained from Jackson Laboratories was maintained by crossing 5XFAD mice with a wild-type (WT) C57BL/6J strain. The 5XFAD mice were maintained as heterozygous.
Dynamic PET imaging. The dynamic acquisition was divided into twelve 5 sec frames, four 60 sec frames, five 120 sec frames, three 5 min frames, and six 10 min scans. The data from all possible lines of response (LOR) were saved in the list mode raw data format. The raw data were then binned into 3D sinograms with a span of 3 and ring difference of 47. The images were reconstructed into transaxial slices (128×128×159) with voxel sizes of 0.0815×0.0815×0.0796 cm3, using the MAP algorithm with 16 subsets, 4 iterations, and a beta of 0.0468. For anatomical co-registration, immediately following the PET scans, the mice received a CT scan in a NanoSPECT/CT (Mediso, Wash. D.C.) at an X-ray beam intensity of 90 mAs and x-ray peak voltage of 45 kVp. The CT images were reconstructed into 170×170×186 voxels at a voxel size of 0.4×0.4×0.4 mm3. The PET/CT images were uploaded into Amide software (www.sourceforge.com), co-registered to an MRI template made in-house, and volumetric regions-of-interest were drawn around the cortex, hippocampus, striatum, thalamus, and cerebellum in addition to the whole brain. The PET images were normalized to the injected dose, and the time-activity-curves (TACs) of the mean activity within the ROIs were estimated for the entire duration of the scans.
Cardiac perfusion procedure and tissue collection. A sharp incision into the abdomen of the anesthetized mouse was made, followed by a longitudinal cut with a scalpel to open the thoracic cavity, which then was stabilized with a retractor. Perfusion began with a 20-gauge syringe containing ice cold PBS (30 ml, pH 7.4) in the left ventricle while the atrium was snipped off. This was followed by injection of paraformaldehyde (PFA) solution (4%). Once the perfusion was completed, the animals were decapitated, and the brains were quickly removed and fixed in PFA overnight at 4° C. followed by sucrose precipitation (30%) overnight at 4° C. The brains were then embedded in Cryo-OCT compound (Fisher Scientific) before sectioning.
Ex vivo brain cross-sections processed for GFAP and IBA1 Immunohistochemistry. The embedded brains in OCT were cut into coronal sections (10 μm) using a Tissue-Tek cryostat and mounted onto charged glass slides. Prior to staining, slides were washed with PBS (3×, 5,5, and 10 min); then, they were treated with blocking buffer (5% normal goat serum, 0.2% Triton X-100, 0.5% bovine albumin in PBS) for 1 h at room temperature. The treated sections were then incubated overnight at 4° C. with primary anti-GFAP antibody (1:100 dilution, Biolegend San Diego, Calif., USA) or anti-IBA1 antibody (1:250 dilution, FUJIFILM Wako Chemicals U.S.A Corporation Richmond, Va., USA). Slides were washed with PBS (3×) for 10 min each, the sections stained for GFAP were subsequently incubated with secondary antibody goat anti-mouse Alexa Fluor 488 (1:200 dilution, Thermo Fisher Scientific, Carlsbad, Calif., USA). Sections stained for IBA1 were incubated with secondary antibody goat anti-rabbit Alexa Fluor 680 (1:200 dilution, Thermo Fisher Scientific, Carlsbad, Calif., USA) for 30 min at room temperature. The sections were then washed with PBS twice for 10 minutes and once for 30 minutes, and cover slipped with an antifade mounting medium with DAPI (Vector Laboratories, Burlingame, Calif.) before observation under a fluorescence microscope.
Statistical analysis. Data were converted to 8-bit grayscale and thresholding using Otsu's method; the pixels were quantified using ImageJ software (version 1.53). The data were then imported to GraphPad software (GraphPad Prism version 9.2.0 for Mac) for statistical analysis. The results are presented as mean±SEM. Differences were analyzed with student's t-test, and the results were considered significant at p values<0.05. For the IBA1 data, since the pixels are small due low expression, the RGB channels were separated, and the red channel, which indicates IBA1-positive signal were thresholded and analyzed as described.
ERGO possesses a unique chemical structure, which contains multiple functional groups. Thus, extensive protection and deprotection maneuvers are necessary to generate a precursor for [11C]CH3 labeling. In that case, many potential combinations of protecting groups have been explored to identify the most compatible deployment of these groups and their order. After several attempts, we reported a successful sequential order to reach to the dimethyl amine precursor 6. Basically, to set the stage for the crucial incorporation of the thiol group onto imidazole, the amino and carboxyl groups of histidine were blocked with acidic labile moieties, while the imidazole amine was protected with an Fmoc group. We previously reported that the amine-protecting Boc groups could be removed using TFA in the presence the t-butyl ester at −78° C. [5]. This reaction confers good yield, albeit only with stringent operations and attention to detail. And thus, the reproducibility is moderate in this case, which should come as no surprise since both the Boc and t-butyl ester share a similar acid-catalyzed hydrolysis mechanism (
When the carboxylic group was protected as a methyl ester, the stability of this ester contributes to better overall reaction yield, 24% versus 14% in the case of tert-butyl ester starting from compounds 2 to 6. But that is only a part of the motivation for this development. We found that this new chemistry is more reliable and reproducible, a main feature necessary for any radiopharmaceutical development. It is certain that this improved and robust chemistry will foster more translational value of the probe for in vivo imaging applications.
We have also demonstrated the specificity of the probe for in vivo detection of oxidative stress using an acute inflammatory LPS mouse model [5]. To further understand the implications of oxidative stress in the context of Abeta cascade mechanism, we want to assess whether this probe could report specific activity relevant to a disease that manifests chronic presentation of an array of ROS-induced inflammation like AD [30-34]. As shown in
In corroboration with the PET data, the immunohistochemistry staining of the brain sections showed that the hippocampus of 5XFAD mice exhibit higher expression levels of activated astrocytes and microglia compared to WT mice. The background level of GFAP-positive astrocytes in WT mice was low, but it could be detected; while IBA1-positive microglia (resting state) in WT mice were barely detectable at high resolution (data not shown). The upregulation of activated microglia and astrocytes support the hypothesis that neuroinflammation could be one of the mechanisms by which AD pathology, including Abeta, leads to neuronal death and dysfunction [35]. Particularly, the pro-inflammatory GFAP marker of the reactive astrocytes, those expression has been linked to Abeta plaque load [36-38]. Furthermore, accumulated data in the past showed that GFAP could serve as an early marker associated with brain Abeta pathology [39]. The detection of oxidative stress using the [11C]ERGO radioligand confirms a past report, which showed that the formation of Abeta plaques trigger a proinflammatory response from microglia and astrocytes [40]. Taken together the data obtained from this work suggest that neuroinflammation reflected in activated microglia and astrocytes in this Abeta accumulating model may trap the [11C]ERGO radioligand contributing to the enhanced PET signal in the 5XFAD mice.
In summary, we report an improved synthesis for the robust and reliable production of [11C]ERGO PET radioligand. Further, the in vivo imaging of an AD phenotype using this probe provides a proof-of-principle to demonstrate for the first time that the neuroinflammation associated with AD could be detected non-invasively, and thereby establishes a novel platform for additional work in the future.
Alzheimer's disease (AD) is the most common cause of dementia among elderly people, but the precise factors contributing to its etiology have not yet been determined [1]. In an aging population, dementia will present one of the greatest challenges to society in this century. The mechanisms that regulate neuronal degeneration in AD remain unclear. However, the cytopathological hallmarks of AD appear to be the deposition of extracellular amyloid-β (Abeta) plaques between neurons and the intracellular accumulation of phosphorylated (p)-Tau, which lead ultimately to profound neuronal toxicity and atrophy [2]. As Abeta plaque formation is one of the underlying mechanisms implicated in AD, prevention of such formation, particularly at early disease onset, would be an important goal to eradicate this disease.
Despite decades of research, the pathogenetic mechanisms that initiate Abeta aggregation are still largely unknown. Postmortem studies of AD human brains showed that there is a huge imbalance of oxidant-antioxidant status that leads to cell death and tissue damage [3]. Reactive oxygen species (ROS) play a pivotal role in normal cellular and signaling pathways, albeit excessive generation of ROS leads to harmful effects, including cellular and protein damage [4-6]. Oxidative stress and damage due to ROS have been implicated in the pathogenesis of AD [7]. Extensive studies have highlighted in particular the role of superoxide anion (∘O2−), hydroxyl radical (∘OH), hydrogen peroxide (H2O2), and nitric oxide (NO∘) in the oxidative stress-mediated neurodegeneration of AD [8,9]. The brain is more vulnerable to oxidative stress than any other organs since components of neurons, such as lipids, proteins, and nucleic acids, can be oxidized in AD. These changes in oxidative stress are associated with increased metal levels, inflammation, and Abeta peptides [10]. Postmortem analysis of human AD brains showed that iron (Fe), zinc (Zn), and copper (Cu) are associated with oxidative stress, and they accumulate in the Abeta plaques of these AD patients [11,12]. Others have also demonstrated that these metals have a very high affinity for Abeta42, a major component of amyloid plaques [13]. Notably, these three metals are cofactors in redox reactions, and they can switch between oxidation states through the Fenton mechanism to generate radicals, which catalyze the conversion of inert peptide side chains into very reactive species. For example, Cu+, Fe2+, and Zn+ could (i) act as cofactors with enzymes to convert inert peptide side chains to active and unstable species; (ii) react with H2O2 under stress conditions to generate ∘OH, which in turn induces particular aggregation, ultimately leading to the formation of annular protofibrils and fibrillar Abeta aggregation [14]. This formation of structural aggregates with biophysical properties is associated with high neurotoxicity and neurodegeneration. Control or suppression of these reactions may therefore provide a valid method to slow down disease onset or Abeta accumulation and associated damage.
Mushrooms are a rich source of four bioactive compounds essential to human health, including selenium [15,16], vitamin D [17,18], glutathione [19], and ergothioneine (ERGO) [20,21]. Except for Vitamin D, the remaining compounds are antioxidant agents. Accumulating evidence indicates that ERGO in particular is a physiological antioxidant cytoprotectant [22-25], existing in the body as a water-soluble zwitterion (
To test the biodistribution and pharmacokinetics of ERGO in vivo, we recently reported the development of an [11C]ERGO PET radioligand [32]. Our study suggested that this zwitterion molecule is very easy to formulate for oral administration since it is very polar. Based on our in vivo PET imaging data, we hypothesized that ERGO could serve as an ideal antioxidant for AD since it can be distributed to the brain by an oral route. ERGO uptake is very high in the small intestine, suggesting that there are abundant receptors (OCTN1 (novel organic cation transporter 1)) in the gut that would shuttle the compound to the circulation where it will be distributed to the brain mediated by OCTN1 receptors expressed in the brain parenchyma.
Since ROS and metal products have a profound impact on downstream Abeta pathology, in this work, we investigated whether consumption of ERGO benefits the brain of 5XFAD mice. Our working hypothesis is that this dual ROS/metal scavenging antioxidant will serve as a potent radical inhibitor to prevent Abeta aggregation (
To demonstrate that ERGO has a high affinity for metals, we developed an assay utilizing 2D-HPLC equipped with a nickel column. In principle, nickel is a transition metal like Fe, Cu and Zn. The nickel column can immobilize hexahistidine-tag (His-tag) recombinant proteins, such as recombinant antibodies harboring a His tag (His-Abs). In our experimental design, nickel forms a substantial coordination equilibrium with histidines via the imidazole ring structures to form a stable metal/ligand complex. This assay uses two different buffer reservoirs, a wash buffer (PBS) and an elution buffer (PBS containing 50 mM imidazole). To remove the His-Abs (14 KDa) from the nickel column, the washing buffer was switched to the elution buffer and the His-Abs dislodged from the column were detected by the 2D-HPLC (
We also assessed ERGO's transition metal scavenging using cupric ion chelating (CIC) and ferrous ion chelating (FIC) assays. In these experiments, pyrocatechol violet or ferrozine forms a complex with free Cu(II) or Fe(II), respectively, resulting in a chromophore with a strong absorbance signal. The pyrocatechol violet-COI) complex has an absorbance lambda max (λmax) at 630 nm, and ferrozine-Fe(II) has a λmax at 562 nm. In the presence of ERGO, fewer free metals are available to form these complexes, resulting in less absorbance. Data in
We used a commercially available DCFH-DA (2′,7′-dichlorodihydrofluorescein diacetate) probe to assess the ROS scavenging power of ERGO in HeLa and neuroblastoma SH-SY5Y cells. Upon penetrating the cytoplasm, DCFH-DA is deacetylated by endogenous esterases to a non-fluorescent intermediate, followed by oxidation by free radicals. This generates a continuous and extended conjugation system, resulting in the production of highly fluorescent DCF (2′ 7′-dichlorofluorescein). In an aqueous condition, DCF has a maximal excitation and emission of 495 nm and 529 nm, respectively. Well-adhered HeLa or SH-SY5Y cells previously incubated with DCFH-DA were exposed to a commercial ROS initializer and ERGO concentrations ranging from 0-100 mM. The data in
To address our primary question whether longitudinal consumption of ERGO as a potent antioxidant benefit the brain, three cohorts of animals (n=12 non-treated WT control, n=12 non-treated 5XFAD, and n=18 ERGO-treated 5XFAD) were used (
At the end of the ERGO treatment, mice were transferred to the animal neurobehavior facility to acclimate for at least three days before behavioral assessment. Cognition of WT (n=12), non-treated 5XFAD (n=12) and ERGO-treated 5XFAD (n=18) mice was assessed using a variety of different assays.
We first confirmed that ERGO treatment had no adverse effects on activity or anxiety-like behavior in the animals that could potentially impact the efficacy and translatability of ERGO as an interventional strategy or that would impact interpretation of cognitive behavioral tasks. We used the elevated zero maze (EZM) to assess anxiety-like behaviors of 5XFAD mice following ERGO treatment. All mice had equivalent exploration in the maze as assessed by total distance travelled (F(2, 39)=0.82, p=0.45). Anxiety-like behavior in this task is indexed via exploration of brighter, open areas of the maze compared to darker, enclosed regions, perceived as “safe zones” [33]. Each group spent close to 60% of their time exploring the closed zones suggesting normal exploratory activity (F(2, 39)=0.19, p=0.82) (
Mice were then trained to associate a series of three small (0.5 mV, 1 second) electric shocks with the termination of a 30-second auditory cue in the conditioned fear task. Recall of the shocks was tested by indexing time spent freezing (a fear response) when mice were exposed to the same testing context, or to the previously-paired tone within a novel testing context, 24 and 25 hours following training, respectively. All mice showed a strong memory of the testing environment as evidenced by similar levels of freezing when returned to the original testing chambers (Kruskal-Wallis statistic=0.54, p=0.77) (
Non-invasive, in vivo, and robust assessment of Abeta levels in the brains of treated and non-treated 5XFAD mice were performed using the [11C]PIB PET probe, the chemical structure of which has been described elsewhere [34]. All animals were injected via the tail vein with the same radioisotope dose (˜15 MBq of [11C]PIB) and volume (100 μL/mouse). To test the preventive effect of ERGO, we treated 5XFAD mice starting at the age of 2-month-old. The idea of this work is based on the premise that young 5XFAD mice do not develop Abeta deposits/plaques in the brains until 2-month-old [35]. We found a steady increase of PET signal in non-treated 5XFAD mice (n=5), at the age of 4-month-old (
To confirm the in vivo observations, animals were perfused, and the brain sections were stained with anti-Abeta antibody, 6E10. Our staining data showed that in non-treated 5XFAD mice, Abeta was highly expressed in the brain regions typically susceptible to AD, including the hippocampus, cortex, and the thalamus (
[11C]ERGO PET radioligand detects oxidative stress reduction in ERGO-treated 5XFAD mice Recently, our [11C]ERGO PET radioligand has been demonstrated as an imaging biomarker for oxidative stress in a mouse model of lipopolysaccharides (LPS) [32] and 5XFAD mice [36]. Thus, in this study, [11C]ERGO PET radioligand was used to assess the fluctuation in oxidative stress with respect to ERGO therapy. We observed very modest reduction in PET signal in a 20-min dynamic scan after intravenous (IV) injection, pertaining to oxidative stress in the brains of treated mice (
We also found that other key inflammation-related protein markers were positively correlated with [11C]ERGO PET imaging data, supporting [11C]ERGO PET radioligand as a robust marker for neuroinflammation in AD. In this study, after the PET imaging, animals (non-treated 5XFAD (n=3) and ERGO-treated 5XFAD mice (n=5)) were perfused, and the brain sections were stained with antibodies against GFAP and IBA1 for neuroinflammatory markers astrocytes and microglia, respectively. Data in
The brain consumes a significant amount of glucose, approximately 25% of the body's glucose [37]. It is well known that glucose metabolism is diminished in the early onset of AD. Therefore, [18F]FDG PET imaging to assess glucose levels could be used for AD diagnosis. For this purpose, three cohorts of age-matched mice (6-month-old, n=3 for each cohort), including WT, non-treated 5XFAD and ERGO-treated 5XFAD (6 doses, each 50 mg/Kg during the course of 2 weeks) were studied. Afterward, animals were injected with [18F]FDG probe (15 MBq, 100 μL/mouse) and underwent 20-min dynamic PET scans and CT scans. The data in
There is convincing evidence demonstrating that free radical damage and oxidative stress play a pivotal role in the early onset of AD [38]. Postmortem brain tissues from AD patients have significant extent of oxidative damage associated with extracellular Abeta plaques and intracellular neurofibrillary tangles [39]. Further, metals have been described to be involved in different pathophysiological mechanisms associated with neurodegenerative diseases, including AD [40]. With the availability of magnetic resonance imaging, iron has been mapped in the brain regions usually associated with Abeta deposits in AD [41,42]. Iron accumulation in the Abeta plaques has also been detected by MRI [43]. Another factor that makes the brain more susceptible to oxidation in AD is the presence of transition metals [44], such as Fe, Zn and Cu [45,46]. These metals serve as a catalyst for the redox-generated free radicals, such as hydroxyl radicals, which have been proposed to initiate Abeta aggregation [47]. Free metal ions have been detected with abnormally high concentration in the ageing brain, as well as during several neurodegenerative disorders [11,48-50]. In AD brains, endogenous metals like Fe, Zn, Cu and Fe are found at a higher concentration in Abeta plaques compared to healthy brains [51]. For example, high levels of Cu (400 μM) and Zn (1 mM) were reported in AD brain compared to 70 μM and 350 μM, respectively in healthy brain [11,52].
Taking all these factors into account, it is apparent that reducing levels of ROS levels and/or neutralizing transitions metals which are catalysts for ROS production, would benefit the brain. ROS- and transition metal-chelating therapy [53,54] have been tested in clinical trials for the treatment of AD using antioxidants and chelators, respectively. These trials show that dietary uptake of antioxidant supplements, like vitamin E or both vitamins C and E may lower the risk of AD [55,56]. Likewise, clinical trials using clioquinone derivatives as metal chelators showed reduced cerebrospinal fluid (CSF) Abeta-42 concentration [57]. Despite some initial success, there have been several issues associated with such antioxidants and chelators which have become the subject of debate, including toxicity and the overall limited ability to cross the blood-brain barrier (BBB) [58]. In that regard, ERGO has more advantage given it is a dual ROS/metal scavengers, which can be distributed to the brain independent of the BBB. In this project, we show that treating 5XFAD mice with high doses of ERGO resulted in reduced Abeta burden, oxidative stress and rescue glucose metabolism, and with some modest improved cognition.
This study shows that imaging biomarkers associated with AD pathogenesis may offer a distinct opportunity for monitoring the response to therapy. Interestingly, we observed both cognitive and molecular benefits of ERGO treatment in 4-month-old 5XFAD mice prior to the onset of significant behavioral deficits, and at least 2 weeks after ERGO treatment had been stopped. This suggests either a lasting benefit of the compound, or at least a delay in onset of genotype-associated behavioral and molecular changes. Importantly, ERGO did not have any detrimental impact on activity levels, anxiety-like behaviors or motor learning which would limit its utility as a therapeutic intervention. All three groups of mice were able to learn the cue-context-shock associations as evidenced by increased freezing behaviors during the two test trials. However, learning was weaker in the non-treated 5XFAD mice which appeared to freeze at approximately half of the rate of WT and ERGO-treated 5XFAD animals during the presentation of the cue (tone) in the novel context. This task requires functional connections between hippocampus, frontal cortex, cingulate cortex as well as the amygdala, which may be particularly important in cue retrieval which was preserved by ERGO treatment [59]. Context retrieval is thought to be more directly dependent on hippocampal inputs. While we did not demonstrate a role for ERGO treatment in context retrieval, it should be noted that at this age there were also no deficits in the non-treated 5XFAD mice on this portion of the task. Similarly, we detected no clear deficits in the 5XFAD mice on the novel object recognition task which is also thought to be highly dependent on intact hippocampal function. However, we used a protocol in which the exposure and test trials were separated by approximately 2 minutes. It is possible that had we imposed a longer delay that recall would have been impaired in the 5XFAD mice which would then have allowed a clearer evaluation of any potential beneficial effects of ERGO treatment. It will therefore be important to further assess potential impacts of short- or longer-term ERGO treatment in more cognitively demanding tasks, or in older animals in which cognitive deficits are more widespread.
L-ERGO was purchased from Cayman Chemical (Ann Arbor, Mich.) and used without any further purification, albeit the material was authenticated and confirmed via mass spectrometry and spectrophotometry before use. The compound was diluted in dd. water at room temperature at a concentration of 50 mg/Kg as a fresh stock solution for every gavage treatment.
Liquid Chromatography Mass Spectrometry (LC-MS) was performed on the sample using a Waters Aquity HPLC and a Thermo Fisher LTQ-Orbitrap XL. The MS was operated in FT mode in positive ion mode with 60 k resolution scanning between 200 and 2000. About 10 μL of the sample were injected onto a symmetry 300 C18 3.5 μm, 2.1×100 mm column, and mobile phases A) 0.2% formic acid and 0.05% TFA in water/acetonitrile (9/1) and B) 0.2% and 0.05% TFA in acetonitrile/water/isopropanol (4/1/5) with a flow rate of 300 μL/min. The gradient held steady at 100% phase A for 1 min before changing to 100% phase B at 10 min and holding for 1 min before returning to the starting conditions and re-equilibrating for 3 min. The data collected was examined using Qual Browser software.
On day 1, HeLa cells or SH-SY5Y cells were seeded into a 96-well plate with a density of 10,000 cells/mL. On day 2, the DCFH-DA probe (Cell Biolabs, Inc., San Diego, USA) was formulated in cell culture media (Gibco Dulbecco's Modified Eagle Medium (DMEM) and dispensed to allocated wells at a final concentration of 1×, as recommended by the manufacturer. The plate was then incubated in the dark for 1 h at 37° C. before excess probe was removed, and the cells were washed repeatedly 3 times with Dulbecco's Phosphate-Buffered Saline (DPBS). Then, ERGO solution was added to the designated wells at concentrations ranging from 5 to 100 mM. The free radical initiator solution was prepared at a concentration of 1× as per manufacturer's recommendation and added to all wells. Immediately afterwards, fluorescence measurement began using a microplate reader (Biotek Industries, Agilent Technologies, Winooski, Vt., USA) with an excitation and emission wavelength of 485 nm and 528 nm, respectively. Each ERGO concentration was measured in pentaplicate.
ERGO's metal-binding affinity was tested via a 2D-HPLC equipped with a nickel-based HisTrap HP column (Cytiva, Marlborough, Mass., USA). The 2D-HPLC was performed with a Hitachi LaChrom Elite L-2455 Diode Array Detector linked to a Hitachi L-2130 pump (Hitachi High-Technologies, Corp., Tokyo, Japan). Two reservoirs of the mobile phase, including PBS and PBS with 50 mM imidazole were programmed so that the first 15 min of the run will be covered with 100% PBS, followed by switching to 100% of the eluting buffer which is comprised of PBS with 50 mM imidazole. In a typical experiment, histidine-containing camelid antibodies (250 ng, MW 14 KDa) dissolved in 200 μL PBS were first injected into the HPLC system. In this setup, the histidine-containing camelid antibodies were immobilized in the nickel column exclusively during the first 15 min with PBS buffer. However, when the mobile phase was changed to PBS with large concentration of imidazole, which will compete and displace His-tag from camelid antibodies resulted in the antibody elution. In another experiment, the antibody was injected as described above but with the addition of ERGO (50 nM). Right at the beginning of the run, His-tag camelid antibodies were eluted, indicating that ERGO competes with the His tag for nickel resulting in an early washout of the antibodies. All analyses were performed via the EZChrom Elite software package (Agilent Technologies, Winooski, Vt., USA).
The iron chelating activity of ERGO was determined using a FIC assay, which was obtained from Zen-Bio Inc. (Durham, N.C.). The assay was done on a 96-well plate with triplicated samples, standards, background, and max absorbance wells. All of the assay absorbance values were subtracted from the average background absorbance, comprising of water and assay buffer (1:1). Maximal absorbance was measured by averaging the absorbance values of 3 wells containing only FeSO4 and assay buffer. For the testing wells, each contained FeSO4 (50 μL) and ERGO samples at different concentrations, including 0, 5, 25, 50, and 100 mM. Control wells contained EDTA standards and a solution of FeSO4 (50 μL), except for the background wells. The assays were started by adding ferrozine solution (100 μL, 1×) to each well using a multichannel pipet, with the final volume of each well being 200 μL. The assaying plate was incubated at room temperature for 10 minutes then the plate was read at 562 nm using a Biotek Synergy 4 plate reader. Absorbances were averaged, and the background absorbance was subtracted from the sample and maximum averages (Abstest and Absmax). The ferrous iron chelating percentage was then calculated using the following equation: Ferrous ion chelating (%)=100×(Absmax−Abstest)/Absmax.
The copper chelating activity of ERGO was determined using a CIC assay (Zen-Bio Inc., Durham, N.C.). Assays contained triplicated samples, standards, background, and max absorbance wells. All the assay absorbance values were subtracted from the average background absorbance, comprising of water and assay buffer (1:1). Maximal absorbance was measured by averaging the absorbance values of 3 wells containing only CuSO4 and assay buffer. For the testing wells, each contained CuSO4 (30 μL) and ERGO samples at different concentrations, including 0, 16, 31, 62, 125, 250, 500, and 1000 mM. Control wells contained EDTA standards and a solution of CuSO4 (30 μL), except for the background wells. The plate was incubated at room temperature for 5 minutes. Assays were started by adding pyrocatechol violet solution (8.5 μL, 1×) to each well, with the final volume of each well being 268.5 μL. The assaying plate was incubated at room temperature on a shaker for 10 minutes, followed by an additional 10-minute incubation at room temperature without shaking. The plate was then read at 632 nm using a Biotek Synergy 4 plate reader. Absorbances were averaged, and the background absorbance was subtracted from the sample and maximum averages (Abstest and Absmax). Cupric ion chelating percentage was then calculated using the following equation: Cupric ion chelating (%)=100×(Absmax−Abstest)/Absmax.
A colony of 5XFAD mice obtained from Jackson Laboratories was maintained by crossing with WT C57BL/6J as we reported in the past [60]. The animals were genotyped by polymerase chain reaction (PCR) using DNA obtained from tail or ear tissue samples. After PCR amplification, DNA product was analyzed using a 1% agarose gel; amyloid precursor protein (APP) transgene=377 bp, and presenilin 1 (PSEN1) transgene=608 bp. 5XFAD mice were maintained as heterozygous. Animals were treated with ERGO formula beginning at the age of 2-month-old. Animal experiments were conducted in accordance with the guidelines established by the Vanderbilt University's Institutional Animal Care and Use Committee (IACUC) and the Division of Animal Care and approved by Vanderbilt IACUC.
Mice (2-month-old) were dosed (50 mg/Kg, less than 100 μL) by means of oral gavage. The procedure involves passing a reusable oral gavage needle through the mouth and placing it atop of the esophagus of an awake animal in the way to encourage the animal to swallow the formulation voluntarily. The curvature of the syringe along with the extra smooth round ball stainless steel tip ensured minimal discomfort to the treated animals. Since the gavage procedure involved restraining of the animal, it might cause stress [61], which is a potential confounding experimental endpoint in behavioral assessments. To ameliorate the potential discrepancy between treated and non-treated cohorts, the later underwent the same oral gavage process, but were given only the vehicle, sterilized water (100 μL).
The primary objective of this work was to answer whether ERGO treatment benefits the brain and improves cognition. At the end of ERGO-based therapy, animals were transferred to the Vanderbilt Neurobehavioral Laboratory to acclimate for at least 3 days before testing.
We recorded exploratory activity in open versus closed zones of a standard EZM during a 5-min trial. At the start of the trial, mice were placed in an open zone of the maze and allowed to explore freely while being videotaped from above. The floor of the maze is 5 cm wide. Closed zones had walls of approximately 30 cm height and light levels of 215-280 lux depending on where they were measured. Open zones had a small lip of ˜0.5 cm and light levels of 349-469 lux. Trials were observed by an experimenter in an adjacent room.
All behavioral apparatus were cleaned with 10% ethanol solution between trials to sanitize the equipment and minimize odor trails lefts by previous animals. The animal's location within the maze and distance traveled were analyzed using AnyMaze (Stoelting Co.).
Exploratory locomotor activity was measured in specially designed chambers measuring 27×27 cm (Med Associates), housed in sound-attenuating cases over a 30-min period. Horizontal and vertical activity within the chambers were automatically recorded via the breaking of infrared beams.
Neuromuscular ability and motor learning were assessed using a standard rotarod (Ugo Basile). Mice were placed on a 6-cm wide section of a ridged rod that rotated slowly. The rod began rotating at 4 rpm and ramped up to a maximum speed of 40 rpm by 4 min (total test time 5 min, max speed for final minute). Mice were allowed to complete 3 trials per day on 3 consecutive days. Time to fall was recorded automatically when mice fell from the rod onto a base plate.
Mice were first allowed to habituate to an open arena for 5 min (white acrylic box, approximately 40 cm2) located under a camera to record position and movement during trials. Immediately following this acclimatization phase, each mouse was removed from the arena which was cleaned with 10% ethanol, and two identical objects were placed in the arena in the center of each arena half. Mice were returned to the arena and allowed to freely explore the objects for 6 min. Mice were then once again removed from the arena, which was again cleaned with 10% ethanol. A third identical exemplar of the familiar object was then added to the arena with one novel object. Position of the novel object was balanced across groups. Exploration of the two objects was permitted for 6 min until the trial was terminated. Preference for either object was inferred from exploratory proximity which was recorded automatically using AnyMaze using a target area comprising a circle with diameter 2-cm larger than the target objects. A recognition index was calculated to assess preference for the novel versus the familiar object as time in proximity to the novel object (TN) divided by time spent in proximity to either novel or familiar (TF) objects (TN/(TN+TF)).
Mice were placed in a sound-attenuating chamber with a wire grid floor capable of transmitting an electric shock. All movements were monitored by cameras fixed to the inside of the doors. Training trials were 8 min during which time a 30-second tone was played three times, that co-terminated with a small shock delivered through the metal floor (1 s, 0.5 mA). Following training mice were transferred to a holding cage in a second ante-chamber and were not reintroduced to (naïve) cage-mates until all the mice had undergone training trials. Twenty-four hours following the training trial the mice were exposed to the same chamber to assess memory for the testing context (4-min trial, no tone, no shock). Mice were tested in the same chambers, in the same test order and under the same lighting and other experimental conditions as training. One hour following the context retrieval trial, the mice were tested again in a novel context for which a second identical chamber was used but it was altered by using a white plexiglass wall and floor insert and a 10% vanilla scent placed in a weigh dish within the outer chamber (not accessible to the mouse). During this 4-min trial the previously exposed tone was played during the final 2 min but there was no shock administered. Freezing behavior was monitored automatically.
The dynamic acquisition was divided into twelve 5-second frames, four 60-second frames, five 120-second frames, three 5-min frames, and six 10-min scans. The data from all possible lines of response (LOR) were saved in the list mode raw data format. The raw data were then binned into 3D sinograms with a span of 3 and ring difference of 47. The images were reconstructed into transaxial slices (128×128×159) with voxel sizes of 0.0815×0.0815×0.0796 cm3, using the MAP algorithm with 16 subsets, 4 iterations, and a beta of 0.0468. For anatomical co-registration, immediately following the PET scans, the mice received a CT scan in a NanoSPECT/CT (Mediso, Wash. D.C.) at an X-ray beam intensity of 90 mAs and x-ray peak voltage of 45 kVp. The CT images were reconstructed into 170×170×186 voxels at a voxel size of 0.4×0.4×0.4 mm3. The PET/CT images were uploaded into Amide software (www.sourceforge.com), co-registered to an MRI template made in-house, and volumetric regions-of-interest were drawn around the cortex, hippocampus, striatum, thalamus, and cerebellum in addition to the whole brain. The PET images were normalized to the injected dose, and the time-activity-curves (TACs) of the mean activity within the ROIs were estimated for the entire duration of the scans.
Brains embedded in OCT were cut into sagittal sections (10 μm) using a Tissue-Tek cryostat and mounted onto charged glass slides. Prior to staining, slides were washed with PBS (10 min); then, they were treated with blocking buffer (5% normal goat serum, 0.2% Triton X-100, 0.5% bovine albumin in PBS) for 1 h at room temperature. The treated sections were then incubated overnight at 4° C. with primary anti-GFAP antibody (1:100 dilution, Biolegend San Diego, Calif., USA). Slides were washed with PBS (3×) for 10 min each, the sections were subsequently incubated with secondary antibody goat anti-mouse Alexa Fluor 488 (1:200 dilution, Thermo Fisher Scientific, Carlsbad, Calif., USA) for 30 min at room temperature. The sections were then washed with PBS twice for 10 min and once for 30 min, and coverslipped with an antifade mounting medium (Vector Laboratories, Burlingame, Calif.) before observation under a fluorescence microscope.
Quantitative analysis of the PET imaging and IHC data was performed using imageJ software. The data was imported to GraphPad Prism version 9 for Mac (GraphPad Software, San Diego, Calif., USA) for statistical analysis. Differences between groups were tested using unpaired t-test.
Behavioral data were analyzed using Prism 9 for Mac OS. Single outcome measures for elevated zero maze (EZM) and locomotor activity chambers were analyzed using Univariate ANOVA with Tukey's multiple comparisons post hoc tests following significant omnibus ANOVA. Fear conditioning data were analyzed using non-parametric approaches because data were not normally distributed (Brown-Forsythe test p<0.05). We therefore used Kruskal-Wallis test for single dependent variable (freezing in familiar context). Data were first assessed for significant effects of sex on all outcomes. Since there were no differences observed, data for male and female animals were combined.
Data are given as mean±standard error of the mean (SEM). Different levels of significance were described as *p<0.05, **p<0.01, and ***p<0.0001.
The data obtained from this work demonstrated the potential use of ERGO for treating AD. It is worth noting that the concentration of ERGO used in this therapy and the assay for scavenging ROS is relatively high. Since ERGO is a natural product, it does not have therapeutic efficacy on the same par as pharmaceutical drugs. Two approaches we envision for future applications. One of those would be focusing on prevention. With a high concentration of ERGO in dietary sources, such as in mushrooms, it is anticipated that consumption of mushroom, in the long term, benefits the brain, and it could be helpful for the prevention of AD. Another approach perhaps focuses on converting this natural antioxidant into therapeutic drugs. A general structure-activity relationship (SAR) study conducted by modifying the chemical genetics surrounding ERGO could lead to a potent agent with improved efficacy.
It should be noted that ratios, concentrations, amounts, and other numerical data may be expressed herein in a range format. It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a concentration range of “about 0.1% to about 5%” should be interpreted to include not only the explicitly recited concentration of about 0.1 wt % to about 5 wt %, but also include individual concentrations (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%) within the indicated range. In an embodiment, the term “about” can include traditional rounding according to significant figures of the numerical value. In addition, the phrase “about ‘x’ to ‘y’” includes “about ‘x’ to about ‘y’”.
Many variations and modifications may be made to the above-described embodiments. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims.
This application claims the benefit of and priority to U.S. Provisional Application Ser. No. 63/239,875, having the title “ERGOTHIONEINE PET COMPOUNDS AND METHODS OF USE THEREOF” filed Sep. 1, 2021, the disclosure of which is incorporated herein in by reference in its entirety.
This invention was made with government support under grant number R01AG061138 awarded by the National Institutes of Health (NIH). The government has certain rights in the invention.
| Number | Date | Country | |
|---|---|---|---|
| 63239875 | Sep 2021 | US |
