Patent Application
20120225015
1. Field of Invention
The inventive subject matter relates to a method of diagnosing or predicting the propensity for autism using endogenous cannabinoids and/or cannibinoid receptor expression.
2. Background Art
Autism spectrum disorders (ASD) are a spectrum of psychological conditions characterized by social interaction and communication deficits. Symptoms also include repetitive behavior that appear early in childhood, usually before age 3 years and often are accompanied by abnormalities in cognitive functioning. CDC, MMWR, 58 (SS10:1-20 (2009)) and American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders (4th ed), Washington, D.C. (1994). The prevalence of autism in the United States is approximately 1 in every 110 births (1 in 70 boys). CDC, MMWR, 58 (SS10:1-20 (2009).
ASD encompass a range of behaviorally defined conditions. The five forms of ASD, including: Autism; Asperger syndrome; atypical autism (pervasive developmental disorder-not otherwise specified (PDD-NOS); Rett syndrome; and Childhood Disintegrative Disorder. Asperger syndrome is closest to autism in signs and causes. Rett syndrome and Child Disintegrative Disorder have similar symptoms as autism, but their etiology may be unrelated. Volkmar, et al., J. Child Psychol. Psychiatry, 50: 108-15 (2009).
Two of the prominent features of autism are immune system dysregulation (Pessah, et al., Neurotoxicology, 29:532-545 (2008) and abnormal brain neuron organization (Courchesne, et al., Neuron, 56:399-413 (2007)).
Autism can be co-morbid with tuberous sclerosis (1.2%), fragile X syndrome (0.3%), and congenital rubella syndrome (0.3%), although the attributable proportion of all medical disorders is less than 10%. However, in most cases, the cause of autism is unknown (Fombonne, e., J. Autism Dev. Disord., 33:365-382 (2003)).
The current inventions relates to a method of determining indicia of autism or ASD by quantitating endocannibinoid levels.
An object of the invention is a method of determining the susceptibility of autism or ASD using biological markers comprising measuring endocannabinoid levels.
Another object of the invention is a method of diagnosing autism or ASD by quantitating endocannabinoid levels in a patient. The endocannibinoids comprise either one or more of Δ9-tetrahydrocannabinol (THC); N-arachidonoylethanolamine (anandamide); N-palmitoylethanolamine (PEA); cannabidiol (CBD); 2-arachidonoyl glycerol (2-AG); and N-oleoylethanolamine (OEA),
Another object is to measure endocannibinoids subsequent to acute exposure to acetaminophen or sociability testing.
A further object of the invention is the measurement of endocannibinoid levels, in a diagnostic method or method to determine susceptibility to autism or ASD by quantitating endocannabinoid receptors.
A still further object of the invention is the determination of susceptibility or diagnosis of autism or autism spectrum disorder by quantitating endocannabinoid synthesis and turnover.
The following terms are defined:
“Autism Spectrum Disorder” refers to a group of developmental disabilities that includes: Autism; Asperger syndrome; pervasive developmental disorder not otherwise specified (PDD-NOS or atypical autism); Rett syndrome; and childhood disintegrative disorder.
“Autism” refers to an autism spectrum disorder characterized by a neural development disorder leading to impaired social interaction and communication by restricted and repetitive behavior.
“Cannabinoid” refers to a class of chemical compounds including phytocannabinoids, which are oxygen-containing C21 hydrocarbons found in the plant species Cannabis sativa (i.e., marijuana), including metabolites and synthetic analogues thereof. Cannabinoids include, but are not limited to, cannabinol, Δ9—tetrahydrocannabinol (THC) and cannabidiol). Cannabinoids as used here also refer to chemical compounds which mimic the actions of phytocannabinoids or have similar structure, such as endocannabinoids. Cannabinoids include compounds that have a high affinity for the cannabinoid receptor, such as THC and those cannabinoids that do not, such as cannabidiol.
Endocannabinoids refer to a class of compounds with similar structure to phytocannabinoids but that are found in animals and that activate cannabinoid receptors.
“Diagnostic” refers to identifying the nature of a pathologic condition.
“Susceptibility of autism or autism spectrum disorder” refers to the likelihood of currently exhibiting or exhibiting in the future autism or one of the other autism spectrum disorders.
Endocannabinoids serve as intercellular, neuromodulatory lipid signals. They are involved in a variety of physiological processes including appetite, pain-sensation, mood and memory. Endocannabinoids are derivatives of arachidonic acid, as well as other poly-unsaturated fatty acids.
Endocannabinoids are endogenous ligands for cannabinoid receptors that are also bound by exogenously introduced cannibinoids, such as THC, the psychoactive component of Cannabis sativa (i.e., marijuana). The cannabis receptors are classified into two groups, CB1 and CB2.
Endocannabinoids include anandamide (N-arachidonoylethanolamine (AEA)), Δ9-tetrahydrocannabinol (THC), N-palmitoylethanolamine (PEA), cannabidiol, N-oleoylethanolamine (OEA), and 2-arachidonoylglyceraol (2-AG). AEA is produced mainly by a transacylase-phosphodiesterase-mediated pathway, initiating from the precursor N-arachidonoyl-phosphatidylethanolamine. The biosynthesis of 2-AG proceeds by rapid hydrolysis of inositol phospholipids by specific phospholipase C generating diacylglyceraol (DAG), which is converted to 2-AG by a sn-1-DAG lipase.
AEA and 2-AG act primarily via cannabinoid receptors. There are seven trans-membrane spanning receptors that belong to the rhodopsin family of G protein-coupled receptors. The binding of endocannabinoids to CB receptors triggers various signaling pathways, such as the inhibition of adenylyl cyclase, the regulation of ionic currents, the activation of focal adhesion kinase, of mitogen-activated protein kinase (MAPK) and of cytosolic phospholipase A2 and the activation of (CB1) or the inhibition (CB2) of nitric oxide synthetase. Both AEA and 2-AG are presumably taken up by cells through a specific carrier, which has not yet been clearly identified. Once inside cells, the cannabinoids are metabolized by multiple pathways.
Plasma endocannabinoid levels have been determined in humans and correlated with a number of maladies, including circulatory disfunction (Quercioli, et al., European Heart Journal 32: 1369-1378 (2011)), and mental health disorders such as anorexia nervosa (Monteleone, et al., Neuropsychopharmacology 30: 1216-1221 (2005)).
The endocannabinoid system plays an important role in the development of the central nervous system. Activation of the endocannabinoid system can induce long-lasting physiological responses (Campolongo et al. Int. Rev. Neurobiol., 85:117-133 (2009)). Use of cannabis (i.e., exogenous cannabinoid) in the still-maturing brain may produce persistent alterations in brain structure and cognition (Jager and Ramsey, Curr. Drug. Abuse Rev., 1: 114-123 (2008)). Animal models have revealed the danger of both cannabis abuse and exposure to cannabinoid drugs during brain development (Anavi-Goffer and Mulder, Chembiochem., 10:1591-1598 (2009)).
Cannibinoid receptors can be classified into two know groups, CB1 or CB2. Developmental problems associated with the endocannabinoid system may occur through either of these two receptor classes.
CB/receptors are located in the central nervous system (CNS), peripheral nervous system, and peripheral organs. In the CNS, CB1 receptors are concentrated in the cerebellum, hippocampus, and the basal ganglia (Drysdale and Platt, Curr. Med. Chem. 10:2719-2732 (2003)), which are areas in the brain implicated as important in autism (Courchesne et al., Neuron 56:399-413 (2007), Bauman and Kemper, Int. J. Dev. Neurosci. 23:183-187 (2005)). During fetal development, CB1 receptors activation is important for neuron differentiation and proper axonal migration (Pride et al., Vitam. Horm. 81:139-158 (2009)). In addition, recent studies suggest that CB1 receptors define synapse positioning (Harkany et al., Cur. Opin. Neurobiol. 18:338-345 (2008)). Modulation of CB1 cannabinoid receptors may also trigger autism by interrupting normal brain development.
CB2 receptors are primarily located in immune tissues and cells and may serve a regulatory function. CB2 receptors have been implicated with regulation of movement of inflammatory cells to the site of injury (Lunn et al., Br. J. Pharmacol. 153:226-239 (2008)). The activation of CB2 receptors may also slow the progression of Alzheimer's disease by stimulating beta-amyloid removal by macrophages (Tolon et al., Brain Res. 1283:148-154 (2009)).
In a preferred embodiment, diagnosis of autism spectrum disorder or autism is determined by a method comprising quantitating endocannibinoid levels. In this embodiment, endocannibinoid levels are quantitated from serum samples collected from patients, ensuring against dietary fluctuations in endocannibinoids (Monteleone, et al., Neuropsychopharmacology, 30: 1216-1221 (2005); Habayeb, et al., JAMA 299: 1135-1136 (2012); Zoerner, et al., Anal Bioanal Chem. (online version: doi:10.1007/s00216-5729-9) (published 4 Feb. 2012)). Deviations of endocannibinoid levels, compared to normal levels, is indicative of autism spectrum disorder or susceptibility to the disorder.
In another embodiment, endocannibinoid levels can be indirectly assessed by quantitating cannibinoid receptor levels. The embodiment avoids any variability inherent in serum endocannabinoid levels. Quantitation of receptors has the added potential advantage of improved accuracy since low levels of endocannibinoids can induce (i.e., upregulate) endocannibinoid receptors in the brain.
In a preferred embodiment, a diagnosis or determination of susceptibility to autism or autism spectrum disorders is made in individuals by first administering high doses of acetaminophen (Kozer, et al., Acta Paediatr., 95: 1165-71 (2006)), typically 12 mg/kg. Alternatively, individuals are subject to sociability testing. Afterwards, the level of plasma endocannibinoids is quantitated. Endocannibinoids include Δ9—tetrahydrocannabinol (THC); N-arachidonoylethanolamine (anandamide); N-palmitoylethanolamine (PEA); cannabidiol (CBD); 2-arachidonoyl glycerol (2-AG); and N-oleoylethanolamine (OEA), wherein said diagnosis or determination of susceptibility is made if the quantitated endocannibinoid level of said individual is different from the mean of the range of individuals, of the same age group, without autism or autism spectrum disorders.
In another embodiment, a diagnosis or determination of susceptibility to autism or autism spectrum disorders is made if the 2-AG level is at least twenty percent (20%), or for AEA, if the AEA level is forty five to seventy five percent (45%-75%), above or below the mean level for non-autistic individuals or individuals without autism spectrum disorders.
Autism is associated with impairments in social interaction; communication; and restricted interests and repetitive behavior. The ability to study the physiological and molecular mechanisms associated with this disease is hampered by suitable models. However, several inbred mouse strains demonstrate inherent behaviors paralleling these sociability impairments. These include the strains BTBR and 129S1/SvImJ (Moy, et al. Behav. Brain Res., 176: 4-20 (2007); McFarlane, et al., Genes Brain Behav., 7: 152-163 (2008); Defensor, et al., Behav. Brain Res., 217: 302-308 (2010); Spencer, et al., Autism Res., 4: 40-56 (2011)).
The social behavior of BTBR mice is sensitive to changes in serotonin (5-HT) neurotransmission and anxiolytics (Gould, et al., J. Neurochem., 116: 291-303 (2011)). Furthermore, administration of the endocannabinoid agonist anandamide or high doses of the pain reliver acetaminophen promote social interactions in mice (Umathe, et al., Prog. Neuropsychopharmacol Biol. Psychiatry, 33: 1191-1199 (2009). Although acetaminophen has little to no affinity for 5-HT receptors, its administration raises 5-HT levels in brain tissue and downregulates 5-HT2 receptors (Courade, et al., Naunyn Schmiedebergs Arch. Pharmacol., 364: 534-537 ((2001); Sandrini, et al., Inflamm. Res., 56: 139-142 (2007)).
CB1 receptors are bound on cell bodies and axons of 5-HT neurons and CB agonists such as WIN 55, 212-2 inhibit presynaptic 5-HT release in brain (Nakazi, et al., Naunyn Schmiedebergs Arch. Pharmacol., 361: 19-24 (2000); Lau and Schloss, Eur. J. Pharmacol., 578: 137-141 (2008)). Acetaminophen's effects on social behavior and analgesic activity are likely to be mediated through its metabolic deacetylation products para-aminophenol and/or N-arachidonoylphenolamine (AM404). These metabolites likely activate CB receptors directly, or indirectly by raising extracellular endogenous CB levels in the brain (Högestätt, et al., J. Biol. Chem., 280: 31405-31412 (2005); Ottani, et al., Eur. J. Pharmacol., 531: 280-281 (2006); Bertolini, et al., CNS Drug Rev., 12: 250-275 (2006); Mallet, et al., PLoS One., 5: e12748 (2010)).
Studies were conducted to determine the affects of acute administration of acetaminophen on social interaction and endogenous cannabinoid levels in the anterior cingulated region of the frontal cortex. These studies were conducted using the socially-impaired mouse strains BTBR and 129S1/SvImJ. The cingulated cortex was targeted because serotonergic tone in this region is linked to anxiety and emotional states that shape social behavior.
BTBR T+tf/J, 129S1/SvImJ and C57BL/6 mouse colony founders were originally obtained from the Jackson Laboratory (Bar Harbor, Me., USA). These strains were bred in the animal facilities of the University of Texas Health Science Center at San Antonio through 2 generations. After weaning at 23-25 days of age, male littermates were housed in groups of 4-5 per cage until behavioral testing at 3-4 months of age. Mice had ad libitum access to food (Teklad™ rodent diet, Harlan, Indianapolis, Ind., USA) and water in ventilated clear plastic cages lined with chipped wood bedding. The housing room had a 12 h light/dark cycle (lights on/off at 7:00) and was maintained at 20-22° C.
Mice were administered acetaminophen (1-400 mg/kg, Sigma, St. Louis, Mo., USA) or 0.9% saline solution by intraperitoneal (i.p.) injection. The cannabinoid agonist WIN55, 212-2 (Ascent Scientific, Princeton, N.J., USA) was dissolved initially in dimethyl-sulfoxide (DMSO Sigma) and was diluted with saline (1:10) to administer 0.1 mg/kg i.p. in 10% DMSO to mice. A sub-group of control mice were treated with 10% DMSO in saline vehicle, these mice did not differ significantly from saline-treated mice in behavioral tests (F1.7<1.25; p>0.3 for all parameters), so the two treatment groups were pooled. Injections were given 30 minutes prior to introduction to the testing arena for conditioning, and 50 min prior to behavior testing.
The three-chamber sociability testing procedure for mice is described in detail in Yang et al. Curr. Protoc. Neurosci., Chapter 8: Unit 8. 26 (2011), our study was conducted in a manner consistent with that protocol. Mice were introduced into the center chamber of an acrylic three-chamber sociability arena, measuring 30×22×61 cm with a light tan bottom, black side walls and two transparent interior walls with slat door openings of 10 cm2 spaced 17 apart dividing the arena into 3 chambers, for 20 min prior to behavioral testing. As described in Gould et al. J. Neurochem., 116: 291-303 (2011), pre-conditioning was performed under low red light (16 lux) at first for 10 min with the mouse confined in the center chamber, then with the doors opened so the subject could explore the entire arena for 10 min longer. Just prior to testing, subjects were briefly confined in the center chamber while an empty wire cup cage was placed at one end of the arena, and a stranger mouse of the same strain was placed under an identical cup cage at the opposite end. Stranger mice were neither litter- nor cage-mates of the subjects and were housed in a separate ventilated cage rack. Stranger mice were pre-conditioned under cup cages in 3 sessions of 30 min each in the day(s) prior to testing, separated by 1 hour reprises in their home cages. Cup cages were topped with weighted jars (9 cm high×7 cm diameter) to prevent mice from climbing on top of them. Digital video cameras (Hewlett-Packard Photosmart™ R742, Palo Alto, Calif., USA) positioned on top of tripods overseeing the arenas were turned on, the doors were removed and social approach behavior was recorded for 10 min under low red light.
The social approach test ended with confinement of the subject into the center chamber and closing of the slat doors. A new stranger mouse was then placed under the empty cup cage, the doors were opened, and behavior was recorded for another 10 min under low red light to assess preference for social novelty. At the end of the test, stranger mice were returned to their home cages for use in subsequent tests, and subject mice were removed from the arena and placed in a marble burying test. The number of boli in the center of the arena was counted prior to cleaning the arena with a solution of 70% EtOH and paper towels prior to conditioning and testing the next animal. Digital videos were analyzed for box entries, time in box and social sniffing time by observers blind to mouse strain or drug treatments.
Marble burying was assessed in a dark room (<16 lux) by placing 15 or 20 blue marbles on top of fresh wood chip bedding filled to a depth of 4-5 cm in a 22×42 cm clear acrylic rat cage covered with a filter top. Mice were placed in the cages to bury marbles for 30 min. Marbles that were at least ⅔ covered by bedding were considered buried, as described previously (Gould et al., J. Neurochem., 116: 291-303 (2011)). Following the marble burying task, mice were sacrificed by cervical dislocation and decapitation; their brains were removed and frozen on powdered dry ice. Cingulate cortex was isolated and stored at −80° C. for subsequent measurement of endocannabinoid levels.
To measure levels of the fatty acid amides 2 arachidonyl glycerol (2-AG), anandamide (AEA), and oleoylethanolamide (OEA), frozen cingulate cortex samples were spiked with 50 pmol of [2H4]anandamide, [2H4]oleoylethanolamine and [2H5]-2-arachidonyl glycerol (internal standards) and processed as in Hardison et al., Prostaglandins Other Lipd Mediat., 81: 106-112 (2006). Briefly, lipids were extracted by adding methanol/chloroform/water (1:2:1, v/v/v) and the chloroform layer was further purified by solid phase extraction using C18 Bond Elut cartridges (100 mg; Varian, USA). Endocannabinoid-containing fractions were analysed by gas chromatography/chemical ionization mass spectrometry (GC/MS) using an isotope dilution assay as described in Seillier et al. Int. J. Neuropsychopharmacol., 3: 373-386 (2010).
The dose-response relationship for acetaminophen (1-400 mg/kg i.p.) to promote dwelling near a stranger mouse in the three chamber social approach test was initially determined in adult male BTBR mice. The lowest dose of acetaminophen to significantly increase time spent in the chamber with a stranger mouse above that of saline-injected controls was 100 mg/kg (F4.25=4.6, p<0.01), as illustrated in
In subsequent three-chamber sociability tests, global repeated-measured ANOVA revealed significant interactions among acute drug treatments, test phase (social approach vs. social novelty) and duration of time spent in each side chamber (FINTERACTION 2.31=7.21, p<0.005). In the social approach test, there was a significant interaction between drug treatment and chamber preference in adult male BTBR mice as determined by mixed-model ANOVA (FINTERACTION 2.31=5.3, p<0.01), Acetaminophen (100 mg/kg) treated BTBR mice spent more time in the chamber with the stranger mouse and less time in the chamber with the empty cage than either vehicle controls (saline±10% DMSO) or WIN 55, 212-2 (0.1 mg/kg) treated mice (F2.31≧4.8. p<0.025) (
Adult male 129S1/SvImJ (129S) mice exhibited global differences in chamber dwelling patterns among drug treatments (F2.24=7.4, p<0.003) and across the two sociability test phases (F1.24=5.0, p<0.03), without interaction, in repeated-measures ANOVA comparisons. In the social approach test, all groups spent essentially equal time in the chamber with a stranger mouse and in the chamber with an empty cage (
BTBR mice that were either treated with acetaminophen and returned to home cages, or were saline-treated subjects in sociability tests had significantly higher anandamide (AEA) levels in frontal cortex (drug effect and interaction F1.19>4.11, p≦0.05, Fisher's LSD post hoc p<0.05, N=5-7) than saline-treated controls, but these effects were not additive, as shown in
In contrast, neither sociability testing nor acetaminophen treatment increased anandamide levels in the frontal cortex of 129S1/SvImJ (129S) mice. Instead, all treatments reduced anandamide levels by ˜20% relative to saline treated, behavior naïve controls (drug effects F1.25=4.29, p<0.05; Fisher's LSD p<0.05), as shown in
In other studies, in BTBR mice, acetaminophen had significant affect on 2-AG levels. In these studies, BTBR and C57BL/6 mice, in early (18 to 21 days postnatal) development, were administered either 4 daily saline or 10% DMS/saline injections; 4 daily injections (i.p.) of 100 mg/kg acetaminophen; 1 injection (i.p.) of 400 mg/kg valproic acid or 4 daily injections (i.p.) 0.01 mg/kg of WIN 55,212-2 for 2 months (i.e., 59 days). The mice were then tested for marble burying and evaluated for neurochemical measures. As shown in
The results show that acute changes in social behavior of adult male mice, with inherently low sociability, are modulated by indirect activation of CB1 receptors by elevated levels of the endocannabinoids anandamide in BTBR mice and 2-AG in 129SvImJ mice in the cingulate region of the frontal cortex. As such, the level of anandamide is an indicator of social disfunction associated with autism spectrum disorders.
The pain-relieving properties of acetaminophen appear to be mediated, in part, through cannabinoid CB1 receptor activation and serotonin (5-HT) system modulation. Acetaminophen is unlikely to act as a direct agonist at CB1 receptors, instead the FAAH inhibitor/CB ligand AM404 is produced through its metabolism, and AM404 increases levels of endogenous cannabinoids such as anandamide and 2-AG in extracellular fluid to activate CB1 receptors indirectly (Högestätt et al., 2005; Bertolini et al., 2006; Schultz, 2010). Based on the results of these studies, quantitation of endocannibinoids, such as annadamide, are of value in diagnosing or determining susceptibility to autism spectrum disorders.
Cannabinoid receptors modulate serotonin signaling in the cingulated cortex region. Serotonergic tone is greater in the frontal cortex of fatty acid amide hydrolase (FAAH) knock-out mice. Their social behavior is enhance, presumably due to higher levels of endogeneous cannabinoid-agonist anandamide (Cassano, et al., Pschopharmacology. 214: 465-476 (2011)). In CB1 knock-out mice serotonergic tone is low, extracellular serotonin levels and serotonin synthesis are elevated in the frontal cortex with a reduced sociability in stressful new habitats relative to wild-type mice (Aso, et al., J. Neurochem. 109: 935-944 (2009); Haller, et al., Eur. J. Neurosci., 19: 1906-1912 (2004)).
Endocannibinoids can be indirectly assessed by measuring expression of endocannibinoid receptors. In a preferred embodiment, positron emission tomography (PET) is used to measure CB1 receptor levels in the brain. In other embodiments, PET can be combined with computed tomography (CT) or magnetic resonance imaging (MRI) scans. This embodiment will enable discernment of receptor expression as a function of anatomical structure.
PET is a nuclear imaging technique that produces three dimensional images of functional processes in the body. Typically, the system is used for the detection of gamma rays emitted indirectly by a position-emitting radionuclide tracer, which is introduced into the body attached to a biologically active molecule.
An embodiment of the inventive method is the analysis of cannibinoid receptors following the introduction of radio-labeled endocannibinoid receptor ligand, such as anandamide or 2-AG, or functional analogs of these molecules, into patients. Although any radio-labeled tracer, suitable for PET can be used, in a preferred embodiment, radio-labeled agonists of CB1 receptors, or their analogs, can be utilized, such as taranabant (N-[(1S,2S)-3-(4-Chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl]-2-methyl-2-((5-(trifluoromethyl) pyridine-2-yl)oxy)propanamide). As examples, the following are potential tracer molecules: In other embodiments, suitable radiolabels include: [11C]CB-119; [11C]JHU75528; [18F]MK9470; and [11C]MePPEP (Hamill, et al., Mol. Imagining biol. 11:246-252 (2009)).
The raw data collected through PET (i.e., coincidence events) are then grouped into projection images (i.e., sonograms). After raw data collection, the data is pre-processed in order to remove artifacts, such as: random coincidences, estimation and subtraction of scattered photons, detector dead-time correction and detector-sensitivity correction, etc. Reconstruction of the final image is conducted by any number of available algorithms. These include filtered back projection and iterative expectation-maximization algorithms. In a preferred embodiment, correction for differential attenuation of photons will be corrected.
Receptors levels determined through analysis of PET imaging will be directly compared to that for normal, non-autistic levels. Higher cannabinoid receptor levels, compared to receptors levels found in children of similar age, is diagnostic of autism or ASD or susceptibility of disease.
Studies suggest that serotonin is important for aspects of prenatal and postnatal brain development (Chugani, D. D., Mol. Psychiatry. 7:S16-S17 (2002); Gasper, et al, Nat. Rev. Neurosci 4:1002-1012 (2003)). Serotonergic function has been reported in children with autism (Hoshino, et al., Neuropsychobiology 11:22-27 (1984); Anderson, et al., J. Child Psychol. Psychiatry 28:885-900 (1987); Cook, et al., J. Neuropsychicatry Clin. Neurosci. 2:268-274 (1990). It was subsequently shown that serotonin synthesis is altered in patients with autism (Chandana, et al., Int. J. Devl. Neuroscience 23:171-182 (2005). In these studies, children with autism exhibit a difference in the change with age in whole brain serotonin synthesis capacity, compared to age matched non-autistic children. Additionally, autistic children also exhibited abnormal cortical asymmetries of serotonin synthesis affecting either the left or right cortex.
The current method utilizes, as indicia of autism or ASD, direct quantitative analysis of endocannibinoid levels. In one embodiment, serum samples of patients are collected and the endocannibinoid levels quantitated by a number of techniques. Examples of quantitation methods include, but are not limited to, liquid chromatographic and mass spectroscopy (Palandra, et al, 0.1. Chromatog B. 887:2052-2060 (7009); Sipe, et PLoS ONE 5:e8792 (2010).
In an additional embodiment, quantitative assessment of endocannibinoids, is conducted by analysis of turnover of endocannibinoid metabolites. In this embodiment, radio-labeled precursors include any precursor of endocannabinoids. Examples include, but are not limited to, N-arachidonoyl phosphatidylethanolamine (NAPE); arachidonic acid and cephalin (AEA) and/or using the 2-AG precursor diacylglyceraol. Analysis of the conversion of these precursors can be quantitatively assessed by any of a number of ways. In one embodiment, assessment is conducted quantitation of radio-labeled endocannibinoids, bound to receptors, by PET. Alternatively, blood samples can be obtained and quantitative assessment of radio-labeled cannibinoids monitored by liquid chromatography and mass spectroscopy.
Alternative to quantitative assessment of metabolites, metabolic byproducts can be analyzed. For example, anandamide, an endocannibinoid, is hydrolyzed by fatty acid amide hydrolase (FAAH) into free arachidonic acid and ethanolamine. Arachidonic acid can be combined with p-aminophenol, a breakdown product of acetaminophen, to form AM404. In one embodiment, paracetamol can be administered to patients. Serum samples can then be analyzed for quantitative assessment of AM404 levels. Alternatively, radio-labeled paracetamol can administered and AM404 levels analyzed by PET.
Having described the invention, one of skill in the art will appreciate in the appended claims that many modifications and variations of the present invention are possible in light of the above teachings. It is therefore, to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described.
This application claims the benefit of U.S. Provisional Application No. 61/448,891, filed 3 Mar. 2011.
| Number | Date | Country | |
|---|---|---|---|
| 61448891 | Mar 2011 | US |
