Effects induced by cannabinoids on monoaminergic systems in the brain and their implications for psychiatric disorders |
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Authors: | Esteban Susana García-Sevilla Jesús A |
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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 |
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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. |
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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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