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Effects induced by cannabinoids on monoaminergic systems in the brain and their implications for psychiatric disorders
Authors:Esteban Susana  García-Sevilla Jesús A
Affiliation:Laboratorio de Neurofarmacología, Institut Universitari d'Investigació en Ciències de la Salut (IUNICS), Universitat de les Illes Balears (UIB), Palma de Mallorca, Spain. susana.esteban@uib.es
Abstract:The endocannabinoid system and CB(1) receptors participate in the control of emotional behavior and mood through a functional coupling with the classic monoaminergic systems. In general, the acute stimulation of CB(1) receptors increases the activity (spontaneous firing rate) of noradrenergic (NE), serotonergic (5-HT) and dopaminergic (DA) neurons as well as the synthesis and/or release of the corresponding neurotransmitter in specific brain regions. Notably, the antagonist/inverse agonist rimonabant (SR141617A) can decrease the basal activity of NE and 5-HT neurons, suggesting a tonic/constitutive regulation of these neuronal systems by endocannabinoids acting at CB(1) receptors. Monoaminergic systems are modulated via CB(1) receptors by direct or indirect effects depending on the localization of this inhibitory receptor, which can be present on monoaminergic neurons themselves and/or inhibitory (GABAergic) and/or excitatory (glutamatergic) regulatory neurons. The repeated stimulation of CB(1) receptors is not associated with the induction of tolerance (receptor desensitization) on the activity of NE, 5-HT and DA neurons, in contrast to chronic agonist effects on neurotransmitter synthesis and/or release in some brain regions. CB(1) receptor desensitization may alter the direct and/or indirect effects of cannabinoid drugs modulating the functionality of monoaminergic systems. The sustained activation of monoaminergic neurons by cannabinoid drugs can also be related to changes in the function of presynaptic inhibitory α(2)-adrenoceptors or 5-HT(1A) receptors (autoreceptors and heteroreceptors), whose sensitivity is downregulated or upregulated upon chronic CB(1) agonist exposure. The functional interactions between endocannabinoids and monoaminergic systems in the brain indicate a potential role for CB(1) receptor signaling in the neurobiology of various psychiatric disorders, including major depression and schizophrenia as the major syndromes.
Keywords:ACEA, arachidonoyl-2-chloroethylamide   Am, basolateral amygdala   AM251, N-(piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide   AM281, 1-(2,4-dichlorophenyl)-5-(4-iodophenyl)-4-methyl-N-4-morpholinyl-1H-pyrazole-3-carboxamide   CB, cannabinoid   CC, cerebral cortex   CNS, central nervous system   CP55,940, (−)-cis-3-[2-hydroxy-4-(1,1-dimethylheptyl)phenyl]-trans-4-(3-hydroxypropyl)cyclohexanol   DA, dopamine   dopa, 3,4-dihydroxy-phenylalanine   DPAT, (±)-8-hydroxy-2-(di-n-propylamino)-tetralin   DR, dorsal raphe   FAAH, fatty acid amide hydrolase   FADD, Fas-associated protein with death domain   GABA, γ-aminobutyric acid   GLU, glutamate or glutamic acid   GPCR, G protein-coupled receptor   GTPγS, guanosine triphosphate   HC, hippocampus   HT, hypothalamus   5-HT, 5-hydroxytryptamine or serotonin   5-HTP, 5-hydroxy-tryptophan   HU210, (6aR)-trans-3-(1,1-dimethylheptyl)-6a,7,10,10a-tetrahydro-1-hydroxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol   LC, locus ceruleus   LH, lateral habenula   MK-801, dizolcipine   NAcc, nucleus accumbens   NE, norepinephrine   NMDA, N-methyl-d-aspartate   PAG, periaqueductal gray matter   PFC, prefrontal cortex   PrH, prepositus hypoglossal nucleus   PW, precipitated withdrawal   SN, substantia nigra   SR141617A, rimonabant   St, corpus striatum   SW, spontaneous withdrawal   TH, tyrosine hydroxylase   THC, Δ9-tetrahydrocannabinol   TPH, tryptophan hydroxylase   URB597, cyclohexyl carbamic acid 3′-carbamoyl-biphenyl-3-yl ester   VTA, ventral tegmental area   WIN55,212-2, R-(+)-[2,3-dihydro-5-methyl-3-[(morpholinyl)-methyl]pyrrolol[1,2,3-de]-1,4-benzoxazinyl]-(1-naphthalenyl) methanone
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