Patent Application
20080039513
Organic solvent extracts, in particular the isopropanolic extract, of the marine sponges Aplysina cavernicola and a mixture of Aplysina fulva and Oceanapia showed VDCC blocker activity and some additionally showed AChE and BuChE enzymes inhibition.
Those compounds that exhibited a neuroprotective effect were selected and further assayed in SH-SY5Y cells loaded with Fluo-4 to measure their effects on changes in intracellular Ca2+in response to depolarization with KCl . The AChE and BuChE inhibitory activities of some of the compounds have also been evaluated following the Ellman's method (Ellman's et al., 1961, Biochem Pharmacol, 7, 88-95). All of them showed inhibition of these enzymatic activities in the 10−5 M range.
After careful investigations, the authors of the invention have found that a family of compounds, some of them present in the marine sponges Aplysina cavernicola, Aplysina Fulva and Oceanapia, block VDCC; some of the compounds additionally inhibit AChE and BuChE. The property of blocking VDCC could be a good approach in the treatment of AD and some other cognitive and neurodegenerative diseases. The combination of this property with the inhibition of AchE and BuChE could be even a better approach.
The present invention provides, as stated above, the use of a structurally distinct family of compounds of formula I, some of them present in the marine sponges Aplysina cavernicola, Aplysina Fulva and Oceanapia, which block VDCC and some additionally show AChE and BuChE inhibition, in the manufacture of a medicament for the treatment of cognitive, neurodegenerative and prion diseases.
Cognitive, neurodegenerative and prion diseases within the meaning of the present invention are, but not limited to, cognitive disorders as senile dementia, cerebrovascular dementia, mild recognition impairment, attention deficit disorder, and/or neurodegenerative dementing disease with aberrant protein aggregations as specially Alzheimer's disease or condition, stroke or prion disease as Creutzfeld-Jakob disease or Gerstmann-Straussler-Scheinker disease.
Characteristic of the compounds is the presence of a heterocyclic unit comprising a spiro ring connected to another spiro ring, an imidazole ring or an amide group through a linker of a length between a certain range. The compounds are represented by formula I:
wherein
L is a linker, consisting of a lineal sequence of 3-20 units selected from the group formed by —CR6R7—, —CR6=,=CR6—, —CO—, —C=NR8, —O—, —S—, substituted or unsubstituted arylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocyclylene, or —NR8—, in any order;
the dotted line represents one or two optional double bonds;
R1 to R5, R10 and R11 are independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclyl, —CORa, —C(O)ORa, —OC(O)Ra, —C(O)NRaRb, —C=NRa, —CN, —ORa, —S(O)t—Ra, —NRaRb, —NRaC(O)Rb, —NO2, —N=CRaRb or halogen;
R6, R7 and R8 are independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted aryl, substituted or unsubstituted aralkyl, substituted or unsubstituted heterocyclyl, —CORa, —C(O)ORa, —OC(O)Ra, —C(O)NRaRb, —C=NRa, —CN, —ORa, —S(O)t—Ra, —NRaRb, —NRaC(O)Rb, —NO2, —N=CRaRb or halogen;
Ra and Rb are each independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted aryl, substituted or unsubstituted aralkyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted alkoxy, substituted or unsubstituted aryloxy or halogen;
t is 0, 1, 2 or 3;
or a tautomer, enantiomer, a pharmaceutically acceptable salt, a prodrug or a solvate thereof.
Preferably the linker contains one or more amide units of the type —CONRa— or —NRaCO—, more preferably there are two units. Even more preferably the linker L means —CO—NH—(L')y—NH—CO—, wherein y is selected from 2, 3, 4, 5, 6, 7, 8, 9 or 10 and L' in between the amide units is formed by units as above defined.
In a preferred embodiment, R2 and R4 are —Br, R3 is —OCH3 and R1 is OH.
In the above definition of compounds of formula (I) the following terms have the meaning indicated:
“Alkyl” refers to a straight or branched hydrocarbon chain radical consisting of carbon and hydrogen atoms, containing no saturation, having one to eight carbon atoms, and which is attached to the rest of the molecule by a single bond, e.g., methyl, ethyl, n-propyl, i-propyl, n-butyl, t-butyl, n-pentyl, etc. Alkyl radicals may be optionally substituted by one or more substituents such as a halo, hydroxy, alkoxy, carboxy, cyano, carbonyl, acyl, alkoxycarbonyl, amino, nitro, mercapto and alkylthio.
“Aryl” refers to a phenyl, naphthyl, indenyl, fenanthryl or anthracyl radical, preferably phenyl or naphthyl radical. The aryl radical may be optionally substituted by one or more substituents such as hydroxy, mercapto, halo, alkyl, phenyl, alkoxy, haloalkyl, nitro, cyano, dialkylamino, aminoalkyl, acyl and alkoxycarbonyl, as defined herein.
“Aralkyl” refers to an aryl group linked to an alkyl group. Preferred examples include benzyl and phenethyl.
“Cycloalkyl” refers to a stable 3- to 10-membered monocyclic or bicyclic radical which is saturated or partially saturated, and which consist solely of carbon and hydrogen atoms. Unless otherwise stated specifically in the specification, the term “cycloalkyl” is meant to include cycloalkyl radicals which are optionally substituted by one or more substituents such as alkyl, halo, hydroxy, amino, cyano, nitro, alkoxy, carboxy and alkoxycarbonyl.
“Halogen” refers to bromo, chloro, iodo or fluoro.
“Heterocyclyl” refers to a stable 3- to 15 membered ring radical which consists of carbon atoms and from one to five heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, preferably a 4- to 8-membered ring with one or more heteroatoms, more preferably a 5- or 6-membered ring with one or more heteroatoms. For the purposes of this invention, the heterocycle may be a monocyclic, bicyclic or tricyclic ring system, which may include fused ring systems; and the nitrogen, carbon or sulfur atoms in the heterocyclyl radical may be optionally oxidised; the nitrogen atom may be optionally quaternized; and the heterocyclyl radical may be partially or fully saturated or aromatic. Examples of such heterocycles include, but are not limited to, azepines, benzimidazole, benzothiazole, furan, isothiazole, imidazole, indole, piperidine, piperazine, purine, quinoline, thiadiazole, tetrahydrofuran.
The terms “arylene”, “cycloalkylene” and “heterocyclylene” refer to aryl, cycloalkyl and cycloalkyl groups having two free radicals.
The dotted line in the ring means that two double bonds can be present in the underlined part of said ring.
References herein to substituted groups in the compounds of the present invention refer to the specified moiety that may be substituted at one or more available positions by one or more suitable groups, e.g., halogen such as fluoro, chloro, bromo and iodo; cyano; hydroxyl; nitro; azido; alkanoyl such as a Cl-6 alkanoyl group such as acyl and the like; carboxamido; alkyl groups including those groups having 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms and more preferably 1-3 carbon atoms; alkenyl and alkynyl groups including groups having one or more unsaturated linkages and from 2 to about 12 carbon or from 2 to about 6 carbon atoms; alkoxy groups having one or more oxygen linkages and from 1 to about 12 carbon atoms or 1 to about 6 carbon atoms; aryloxy such as phenoxy; alkylthio groups including those moieties having one or more. thioether linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; alkylsulfinyl groups including those moieties having one or more sulfinyl linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; alkylsulfonyl groups including those moieties having one or more sulfonyl linkages and from 1 to about 12 carbon atoms or from I to about 6 carbon atoms; aminoalkyl groups such as groups having one or more N atoms and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; carbocylic aryl having 6 or more carbons, particularly phenyl or naphthyl and aralkyl such as benzyl. Unless otherwise indicated, an optionally substituted group may have a substituent at each substitutable position of the group, and each substitution is independent of the other.
The term “pharmaceutically acceptable salts, derivatives, solvates, prodrugs” refers to any pharmaceutically acceptable salt, ester, solvate, or any other compound which, upon administration to the recipient is capable of providing (directly or indirectly) a compound as described herein. However, it will be appreciated that non-pharmaceutically acceptable salts also fall within the scope of the invention since those may be useful in the preparation of pharmaceutically acceptable salts. The preparation of salts, prodrugs and derivatives can be carried out by methods known in the art.
For instance, pharmaceutically acceptable salts of compounds provided herein are synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts are, for example, prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent or in a mixture of the two. Generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol or acetonitrile are preferred. Examples of the acid addition salts include mineral acid addition salts such as, for example, hydrochloride, hydrobromide, hydroiodide, sulphate, nitrate, phosphate, and organic acid addition salts such as, for example, acetate, maleate, fumarate, citrate, oxalate, succinate, tartrate, malate, mandelate, methanesulphonate and p-toluenesulphonate. Examples of the alkali addition salts include inorganic salts such as, for example, sodium, potassium, calcium, ammonium, magnesium, aluminium and lithium salts, and organic alkali salts such as, for example, ethylenediamine, ethanolamine, N,N-dialkylenethanolamine, triethanolamine, glucamine and basic aminoacids salts.
Particularly favoured derivatives or prodrugs are those that increase the bioavailability of the compounds of this invention when such compounds are administered to a patient (e.g., by allowing an orally administered compound to be more readily absorbed into the blood) or which enhance delivery of the parent compound to a biological compartment (e.g., the brain or lymphatic system) relative to the parent species.
Any compound that is a prodrug of a compound of formula (I) is within the scope of the invention. The term “prodrug” is used in its broadest sense and encompasses those derivatives that are converted in vivo to the compounds of the invention. Such derivatives would readily occur to those skilled in the art, and include, depending on the functional groups present in the molecule and without limitation, the following derivatives of the present compounds: esters, amino acid esters, phosphate esters, metal salts sulfonate esters, carbamates, and amides. Examples of well known methods of producing a prodrug of a given active compound are known to those skilled in the art and can be found e.g. in Krogsgaard-Larsen et al. “Textbook of Drug Design and Discovery” Taylor & Francis (April 2002).
The compounds of the invention may be in crystalline form either as free compounds or as solvates and it is intended that both forms are within the scope of the present invention. Methods of solvation are generally known within the art. Suitable solvates are pharmaceutically acceptable solvates. In a particular embodiment the solvate is a hydrate.
The compounds of formula (I) or their salts or solvates are preferably in pharmaceutically acceptable or substantially pure form. By pharmaceutically acceptable form is meant, inter alia, having a pharmaceutically acceptable level of purity excluding normal pharmaceutical additives such as diluents and carriers, and including no material considered toxic at normal dosage levels. Purity levels for the drug substance are preferably above 50%, more preferably above 70%, most preferably above 90%. In a preferred embodiment it is above 95% of the compound of formula (I), or of its salts, solvates or prodrugs.
The compounds of the present invention represented by the above described formula (I) may include enantiomers depending on the presence of chiral centres or isomers depending on the presence of multiple bonds (e.g. Z, E). The single isomers, enantiomers or diastereoisomers and mixtures thereof fall within the scope of the present invention. When a compound is drawn with explicit stereochemistry, it is intended to represent the racemic structure with relative stereochemistry as well as the enantiomers in different degrees of purity. In any case, the enantiomers and diastereoisomers of compounds represented with a particular stereochemistry form also part of the compounds of the invention.
The compounds Aerothionin, Homoaerothionin and 11,19-dideoxyfistularin, isolated from Aplysina cavernicola, are represented by formulae “Compound 3”, “Compound 4” and “Compound 5”:
The compound 3 was described by L. Minale and G. Sodano. J. in J. Chem.Soc.Chem. Commun, 0, 1970, 751-753; whereas compound 4 was described in J.Chem.Soc.Perkin Trans, 0 ,18-24, 1972 and the compound 5 was described by M. R. Kernan, R. C. Camhie in J. Nat. Prod. 1990,53,615-622. None of these documents discloses or suggests that these compounds presented VDCC blocker activity with eventually additional AChE and butyrylcholinesterase (BuChE) inhibitory activities.
From the mixture of Aplysina fulva and Oceanapia the following compounds have been isolated:
Compound 6 was firstly described by Cimino and G. Sodano, in Tetrahedron Letters, 24, 1983, 3029-3032 and compound 7 by Morris and Andersen, Canadian Journal Chemistry, 67, 1989, 677-681.
Compounds 7 and 8 were isolated by subjecting the isopropanolic fraction of the mixture of Aplysina fulva and Oceanopia to a VLC (vaccum-liquid chromatography), eluting with MeOH 100%, and subsequently performing a semi-preparative HPLC. It was isolated as its formic salt, in the form of a pale yellow syrup. Compound 8 is a new compound, and the experimental data which have allowed the elucidation of its structure are the following:
1H δ
13C δ
The present invention further provides a compound of formula:
and pharmaceutical compositions comprising such a compound, or a pharmaceutically acceptable salt, derivative, prodrug or stereoisomers thereof together with a pharmaceutically acceptable carrier, adjuvant, or vehicle, for administration to a patient. Although represented as the formiate salt, other pharmaceutically acceptable salts are also possible and are within the scope of the present invention.
Examples of pharmaceutical compositions include any solid (tablets, pills, capsules, granules etc.) or liquid (solutions, suspensions or emulsions) composition for oral, topical or parenteral administration.
In a preferred embodiment the pharmaceutical compositions are in oral form, either solid or liquid. Suitable dose forms for oral administration may be tablets, capsules, syrops or solutions and may contain conventional excipients known in the art such as binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, or polyvinylpyrrolidone; fillers, for example lactose, sugar, maize starch, calcium phosphate, sorbitol or glycine; tabletting lubricants, for example magnesium stearate; disintegrants, for example starch, polyvinylpyrrolidone, sodium starch glycollate or microcrystalline cellulose; or pharmaceutically acceptable wetting agents such as sodium lauryl sulfate.
The solid oral compositions may be prepared by conventional methods of blending, filling or tabletting. Repeated blending operations may be used to distribute the active agent throughout those compositions employing large quantities of fillers. Such operations are conventional in the art. The tablets may for example be prepared by wet or dry granulation and optionally coated according to methods well known in normal pharmaceutical practice, in particular with an enteric coating.
The pharmaceutical compositons may also be adapted for parenteral administration, such as sterile solutions, suspensions or lyophilized products in the apropriate unit dosage form. Adequate excipients can be used, such as bulking agents, buffering agents or surfactants.
The mentioned formulations will be prepared using standard methods such as those described or referred to in the Spanish and US Pharmacopoeias and similar reference texts.
Administration of the compounds or compositions of the present invention may be by any suitable method, such as intravenous infusion, oral preparations, and intraperitoneal and intravenous administration. Oral administration is preferred because of the convenience for the patient and the chronic character of the diseases to be treated.
Generally an effective administered amount of a compound of the invention will depend on the relative efficacy of the compound chosen, the severity of the disorder being treated and the weight of the sufferer. However, active compounds will typically be administered once or more times a day for example 1, 2, 3 or 4 times daily, with typical total daily doses in the range of from 0.1 to 1000 mg/kg/day. It will be appreciated that it may be necessary to make routine variations to the dosage, depending on the age and condition of the patient, and the route of administration.
The compounds and compositions of this invention may be used with other drugs to provide a combination therapy. The other drugs may form part of the same composition, or be provided as a separate composition for administration at the same time or at different time.
The compounds of formula (I) defined above can be obtained by a convergent pathway strategy by coupling the two heterocyclic moieties which contain part of the linker. Synthetic procedures for preparing the compounds of formula (I) are described by Wasserman, H. et al. in J. Org. Chem. 1998, 63,5581-5586, and by Nishiyama S. et al. in Tetrahedron Letters, Vol.24, No. 32, pp. 3351-3352, 1983. The person skilled in the art of organic synthesis will readily design the process for each compound depending on the desired functionality of the heterocycles, the substituents and the nature of the linker to be obtained.
The reaction products may, if desired, be purified by conventional methods, such as crystallisation or chromatography. Where the above described processes for the preparation of compounds of the invention give rise to mixtures of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. If there are chiral centers the compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution.
One preferred pharmaceutically acceptable form is the crystalline form, including such form in a pharmaceutical composition. In the case of salts and solvates the additional ionic and solvent moieties must also be non-toxic. The compounds of the invention may present different polymorphic forms, it is intended that the invention encompasses all such forms.
The compounds of formulas 1 to 5 defined above can also be obtained by isolation of the compound from the marine sponge Aplysina cavernicola, according to the following process which comprises the following steps:
a) effecting an extraction of a previously triturated Aplysina cavernicola with an organic solvent, in particular isopropanol
b) optionally concentrating the organic solvent extract and effecting a water/ether extraction of the product obtained in step a), and
c) effecting a column chromatography of the product obtained in the previous step in order to isolate the individual compounds.
The compounds of formulas 6 to 8 defined above may be obtained by isolation of the compound from a mixture of marine sponges Aplysina fulva and Oceanapia; in the case of Compound 6, it may be isolated according to the following process comprising the steps of:
a) effecting an extraction of a previously triturated mixture of Aplysina fulva and oceanopia with an organic solvent, in particular isopropanol
b) subjecting the isopropanol extract to a vacuum-liquid chromatography eluting with H2O-MeOH 1:1; and
c) performing a semipreparative High Performance Liquid Chromatography.
Compounds 7 and 8 may be isolated by the following steps:
a) effecting an extraction of a previously triturated mixture of Aplysina fulva and oceanopia with an organic solvent, in particular isopropanol
b) subjecting the isopropanol extract to a vacuum-liquid chromatography eluting with MeOH 100%; and
c) performing a semipreparative High Performance Liquid Chromatography.
The invention is also directed to organic solvent extracts of Aplysina cavernicola and Aplysina fulva and Oceanapia; to said extracts for use as medicaments, in particular for the treatment of cognitive disorders as senile dementia, cerebrovascular dementia, mild recognition impairment, attention deficit disorder, and/or neurodegenerative dementing disease with aberrant protein aggregations as specially Alzheimers's disease or condition, stroke or prion disease as Creutzfeld-Jakob disease or Gerstmann-Straussler-Scheinker disease; to the use of said extracts in the manufacture of a medicament, in particular for the manufacture of a medicament for the treatment of brain ischemia, stroke, cognitive disorders as senile dementia, cerebrovascular dementia, mild recognition impairment, attention deficit disorder, and/or neurodegenerative dementing disease with aberrant protein aggregations as specially Alzheimer's disease or condition, or prion disease as reutzfeld-Jakob disease or Gerstmann-Straussler-Scheinker disease; and, finally, to a process for obtaining said extracts from Aplysina cavernicola and a mixture of Aplysina fulva and Oceanapia, as indicated above.
The following examples are given as further illustration of the invention, they should not be taken as a definition of the limits of the invention.
The general procedures for the preparation of the compounds of the invention have been described above.
a) Aplysina cavernicola was collected in 2001 at Ibiza sea (Spain). The sponge forms irregular straplike branches, the surface is conculose with fine protruding fibers, and it is flexible and very difficult to tear. The sponge is deep brownish-yellow in life and cream in preservative.
b) The mixture of Aplysina fulva and Oceanapia (minority) was collected in 2002 at 12 meters depth in Izabal, Guatemala. A voucher specimen (ORMA 006265) is deposited at PharmaMar, Colmenar Viejo, Madrid.
a) A sample of frozen Aplysina cavernicola (600 gr wet weight) was cut into small pieces (2 cm) and triturated, the marine material was extracted with isopropanol (3 L×2). After decantation, the combined extracts were concentrated to give a brown solid (12 gr) and partitioned between diethyleter and water. The organic layer was concentrated to give a brown oil (1.67 gr). The oil was chromatographed on silica gel with a stepwise gradient solvent system: DCM/MeOH (100:1), DCM/MeOH (75:1), DCM/MeOH (50:1), DCM/MeOH (25:1). After this chromatography purification we isolated five compounds and all of them were described as Aeroplysinin-2 (compound 1), Aeroplysinin-1 (compound 2), Aerothionin (compound 3), Homoaerothionin (compound 4), and 11,19-dideoxyfistularin (compound 5).
The compound 1 was described by L. Minale and G. Sodano. J. Chem.Soc.Chem. Commun, 0, 1972, 674-675, the Compounds 2 and 3 were described by the same authors in J. Chem.Soc. Chem. Commun, 0, 1970, 751-753. The Compound 4 was described in J. Chem.Soc.Perkin Trans, 0 ,1 8-24, 1972 and the compound 5 was described in M. R. Kernan, R. C. Camhie. J. Nat. Prod. 1990,53,615-622.
b) The mixture of Aplysina fulva and minority Oceanapia (158 g) was diced and extracted with 2-propanol ( 3×400 ml). The combined extracts were concentrated to yield a crude of 6.42 g. This material was subjected to VLC (vacuum-liquid chromatography) on Lichooprep RP-18, with a stepped gradient from H2O to MeOH.
14 mg of Compound 6 were isolated from the fraction eluting with H2O-MeOH 1:1, followed by a subsequent semipreparative HPLC (High Performance Liquid Chromatography) (AtlantisSemiprep C-18, 10×150 mm, gradient H2O—AcN+0.1% formic acid from 20 to 50% AcN in 30 min UV detection at 254 nm); this compound was disclosed by Cimino and G. Sodano., Tetrahedron Letters, 24, 1983, 3029-3032. 17.33 mg of Compound 7 and 48.77 mg of compound 8 were isolated from the same fraction, eluting with MeOH 100%, followed by a subsequent semipreparative HPLC (SymmetryPrep C-18, 19×300 mm, gradient H2O—AcN+0.1% formic acid from 20 to 100% AcN in 30 min UV detection at 254 nm). Compound 7 was disclosed by Morris and Andersen, Canadian Journal Chemistry, 67, 1989, 677-681. Compound 8 is novel, and has been isolated as its formic salt, in the form of a yellow pail syrup. Experimental data:
a) HPLC was perform with a symmetry C18 (4.6×150 mm, 3.5 μm) column using a Waters Alliance 2695 with a 2996 photodiode array detector and Waters ZQ2000 mass spectrometer used for the analytical separation and for UV and mass determination. The gradient used for the elution was 0-5 min 80% A: 20% B; 5-40 min 100% B; 40-45 min 100% B; 45-46 min 80% A: 20% B (A=H2O 0.1% HF; B=AcN 0.1% HF).
1H, 13C, NMR spectra were recorded on a Varian Mercury 400 MHz spectrometer in CD3OD using the solvent as a reference standard (1H, 4.87, 3.31, and 13C, 49.1). 1H, 13C, COSY, HSQC, HMBC, NOE and DEPT spectra were obtained using standard Varian pulse sequences.
b) Mass spectral analyses were accomplished on a ZQ2000 single quadrupole mass spectrometer (Micromass) fitted with an ESI source and operated in the positive ionization mode.IR Spectra were recorded on a Bruker Tensor 27 FT-IR spectrometer.
1H, 13C, NMR spectra were recorded on a Varian Mercury 400 MHz spectrometer in CD3OD using the solvent as a reference standard (1H, 4.87, 3.31, and 13C, 49.1). 1H, 13C, COSY, HSQC, HMBC, NOE and DEPT spectra were obtained using standard Varian pulse sequences.
In order to find new marine compounds with VDCC blocker activity, we have performed a screening on SH-SY5Y neuroblastoma cells exposed to KCl 120 mM, The ability to block calcium channels is evaluated measuring cellular viability, using the LDH assay. Previously to the depolarization these cells were pretreated for 1 hour with the marine extracts at different concentrations (50, 15 and 5 μg/ml), 24 hours later survival is tested. Those compounds that exhibited a neuroprotective effect were selected and further assayed in SH-SY5Y cells loaded with Fluo-4 (Molecular probes) to measure their effects on changes in intracellular Ca2+in response to depolarization with 60 mM KCl.
SH-SY5Y cells were plated at 5×105 cells per well into Black/Clear Bottom 96-well culture plate, 48 hours before treatment. Cells were loaded with Fluo-4, 5 μM and pluronic acid, 0.1%, for 30 min at 37° C., 5% CO2, following a incubation of 15 min at RT in Krebs-HEPES solution. Immediately cells are exposed to the samples at different concentrations for 10 min. The marine extracts were tested, in Krebs-HEPES, at final concentrations of 50 μg/ml, 15 μg/ml and 5 μg/ml, and the isolated compounds at 10−5, 10−6 and 5×10−8 M. After the treatment, the fluorescence is measured in a Fluostar Optima plate reader (BMG) in response to depolarization with 60 mM KCl. The excitation wavelength was 485 nm, and that of emission 520 nm.
The marine extract from the sponge Aplysina cavernicola showed neuroprotective activity and VDCC blocker activity. Three compounds isolated from this extract have shown calcium channel blocking properties in SH-SY5Y neuroblastoma cells. Results are showed in table 2.
AChE inhibitory activity was evaluated at 30° C. by the colorimetric method reported by Ellman (Ellman, G. L. et al., 1961, Biochem Pharmacol, 7, 88-95). The assay solution consisted of 0.1 M phosphate buffer pH 8, 0.3 mM 5,5′-dithiobis (2-nitrobenzoic acid) (DTNB, Ellman's reagent), 0.02 units AChE (Sigma Chemical Co. from bovine erythrocytes), and 0.5 mM acetylthiocholine iodide as the substrate of the enzymatic reaction. The compounds tested were added to the assay solution and pre incubated with the enzyme for 5 min at 30° C. After that period, the substrate was added. The absorbance changes at 405 nm were recorded for 5 min with a microplate reader Digiscan 340T, the reaction rates were compared, and the percent inhibition due to the presence of test compounds was calculated. The reaction rate was calculated with, at least, triplicate measurements, and the percent inhibition due to the presence of test compound was calculated relative to the compound-free control. The results are shown in table 1.
BuChE inhibitory activity was evaluated at 30° C. by the colorimetric method reported by Ellman (Ellman, G. L. et al., 1961, Biochem Pharmacol, 7, 88-95). The assay solution consisted of 0.01 units BuChE from human serum, 0.1 M sodium phosphate buffer pH 8, 0.3 mM 5,5′-dithiobis (2-nitrobenzoic acid) (DTNB, Ellman's reagent), and 0.5 mM butyrylthiocholine iodide as the substrate of the enzymatic reaction. Enzyme activity was determined by measuring the absorbance at 405 nm during 5 minutes with a microplate reader Digiscan 340T. The tested compounds were preincubated with the enzyme for 10 minutes at 30° C. The reaction rate was calculated with, at least, triplicate measurements. The results are shown in table 2.
The cytotoxicity effect of the molecules was tested in the human neuroblastoma cell line SH-SY5Y. These cells were cultured in 96-well plates in minimum essential medium, Ham's F12 medium, supplemented with 10% fetal bovine serum, 1% glutamine and 1% penicillin/streptomycin, and grown in a 5% CO2 humidified incubator at 37° C. Cells were plated at 104 cells for each well, at least, 48 hours before treatment. Cells were exposed for 24 hours to the compounds at different concentrations (from 10−5 to 10−9), quantitative assessment of cell death was made by measurement of the intracellular enzyme lactate dehydrogenase (LDH) (citotoxicity detection kit, Roche). The quantity of LDH was measured was evaluated in a microplate reader Anthos 2010, at 492 and 620 nm. Controls were taken as 100% viability. The results are shown in table 2.
Propidium exhibits an increase in fluorescence on binding to AChE peripheral site, making it a useful probe for competitive ligand binding to the enzyme. Fluorescence was measured in a Fluostar Optima plate reader (BMG). Measurements were carried out in 100 μl solution volume, in 96-well plates. The buffer used was 1 mM Tris/HCl, pH 8.0. 5 μM AChE was incubated, at least 6 hours, with the molecule at different concentrations. 20 μM propidium iodide was added 10 min before fluorescence measurement. The excitation wavelength was 485 mn and that of emission 620 nm. In vitro results are showed in table 2.
In order to evaluate if these compounds have antioxidant properties, SH-SY5Y cells were exposed for 24 hours to 100 μM H2O2, previously these cells were pretreated for 1 hour with the molecules at different concentrations (from 10−5 to 10−9). The antioxidant activity is evaluated measuring cellular viability, using the LDH assay. Cells SH-SY5Y were cultured in 96-well plates as toxicity experiments. The results are shown in table 2.
| Number | Date | Country | Kind |
|---|---|---|---|
| 04076731.1 | Jun 2004 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP05/06643 | 6/17/2005 | WO | 00 | 1/19/2007 |
