Alcohol and Dopamine

Dopamine is a neuromodulator that is used by neurons in several brain regions involved in motivation and reinforcement, most importantly the nucleus accumbens (NAc). Dopamine alters the sensitivity of its target neurons to other neurotransmitters, particularly glutamate. In addition, dopamine can affect the neurotransmitter release by the target neurons. Dopamine-containing neurons in the NAc are activated by motivational stimuli, which encourage a person to perform or repeat a behavior. Even low alcohol doses can increase dopamine release in part of the NAc. This dopamine release may contribute to the rewarding effects of alcohol and may thereby play a role in promoting alcohol consumption. In contrast to other stimuli, alcohol-related stimuli maintain their motivational significance even after repeated alcohol administration, which may contribute to the craving for alcohol observed in alcoholics.

[1]  A. Zeichner,et al.  The biphasic effects of alcohol on human physical aggression , 1997 .

[2]  B. Bloch,et al.  Phenotypical characterization of the rat striatal neurons expressing the D1 dopamine receptor gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[3]  U. Ungerstedt Stereotaxic mapping of the monoamine pathways in the rat brain. , 1971, Acta physiologica Scandinavica. Supplementum.

[4]  Micaela Morelli,et al.  Modulatory functions of neurotransmitters in the striatum: ACh/dopamine/NMDA interactions , 1994, Trends in Neurosciences.

[5]  G. Di Chiara,et al.  Preferential stimulation of dopamine release in the nucleus accumbens of freely moving rats by ethanol. , 1986, The Journal of pharmacology and experimental therapeutics.

[6]  G. Di Chiara,et al.  Cannabinoid and heroin activation of mesolimbic dopamine transmission by a common mu1 opioid receptor mechanism. , 1997, Science.

[7]  B. Bloch,et al.  Dopamine receptor gene expression by enkephalin neurons in rat forebrain. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[8]  G. Di Chiara,et al.  Intravenous cocaine, morphine, and amphetamine preferentially increase extracellular dopamine in the "shell" as compared with the "core" of the rat nucleus accumbens. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[9]  M. Chesselet,et al.  Presynaptic regulation of neurotransmitter release in the brain: Facts and hypothesis , 1984, Neuroscience.

[10]  G. Di Chiara,et al.  Ethanol preferentially stimulates dopamine release in the nucleus accumbens of freely moving rats. , 1985, European journal of pharmacology.

[11]  C. Cepeda,et al.  Neuromodulatory actions of dopamine in the neostriatum are dependent upon the excitatory amino acid receptor subtypes activated. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[12]  J. Glowinski,et al.  Dopaminergic Terminals in the Rat Cortex , 1973, Science.

[13]  G. Di Chiara,et al.  Blockade of delta-opioid receptors in the nucleus accumbens prevents ethanol-induced stimulation of dopamine release. , 1993, European journal of pharmacology.

[14]  G. Di Chiara,et al.  Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[15]  F. Bloom,et al.  Oral alcohol self-administration stimulates dopamine release in the rat nucleus accumbens: genetic and motivational determinants. , 1993, The Journal of pharmacology and experimental therapeutics.

[16]  F. Muntoni,et al.  Low doses of ethanol activate dopaminergic neurons in the ventral tegmental area , 1985, Brain Research.

[17]  V Bassareo,et al.  Differential Influence of Associative and Nonassociative Learning Mechanisms on the Responsiveness of Prefrontal and Accumbal Dopamine Transmission to Food Stimuli in Rats Fed Ad Libitum , 1997, The Journal of Neuroscience.

[18]  T. Robbins,et al.  Limbic-striatal interactions in reward-related processes , 1989, Neuroscience & Biobehavioral Reviews.

[19]  G. Chiara,et al.  Effects of nicotine on the nucleus accumbens and similarity to those of addictive drugs , 1996, Nature.

[20]  N. Volkow,et al.  Acute effects of ethanol on regional brain glucose metabolism and transport , 1990, Psychiatry Research: Neuroimaging.

[21]  Kitai St,et al.  Cholinergic and dopaminergic modulation of potassium conductances in neostriatal neurons. , 1993 .

[22]  James L Olds Pleasure Centers in the Brain , 1956, Scientific American.

[23]  L. Heimer,et al.  Substantia innominata: a notion which impedes clinical–anatomical correlations in neuropsychiatric disorders , 1997, Neuroscience.

[24]  C. Gerfen The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia. , 1992, Annual review of neuroscience.

[25]  G. Di Chiara,et al.  Localization of nigral dopamine-sensitive adenylate cyclase on neurons originating from the corpus striatum. , 1977, Science.

[26]  William H. Lyness,et al.  Influence of dopaminergic and serotonergic neurons on intravenous ethanol self-administration in the rat , 1992, Pharmacology Biochemistry and Behavior.

[27]  L. Martin,et al.  D1 agonist-induced excitation of substantia nigra pars reticulata neurons: mediation by D1 receptors on striatonigral terminals via a pertussis toxin-sensitive coupling pathway , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  G. Chiara The role of dopamine in drug abuse viewed from the perspective of its role in motivation , 1995 .