Abstract
Acetaldehyde is the first and principal metabolite of ethanol administered systemically. To its rise in blood, after administration of disulfiram, is ascribed the aversive reaction that should discourage alcoholics from drinking. In the present study, we sought to determine the effect of acetaldehyde on the electrophysiological properties of dopamine (DA)-containing neurons in the ventro tegmental area (VTA) of rats in vivo. Intravenous (i.v.) administration of acetaldehyde (5–40 mg/kg) readily and dose-dependently increased the firing rate, spikes/burst, and burst firing of VTA neurons. Ethanol (250–1000 mg/kg/i.v.) administration produced similar increments in electrophysiological parameters. In addition, a second group of rats was pretreated with the alcohol-dehydrogenase inhibitor 4-methyl-pyrazole (90 mg/kg) intraperitoneally (i.p.), and ethanol and acetaldehyde were administered i.v. at the same doses, 48 h later. In this group, ethanol effects were drastically reduced and the firing rate, spikes/burst, and burst firing were not significantly altered. In contrast, acetaldehyde fully retained its capacity to stimulate electrophysiological indices. The results indicate that acetaldehyde produces electrophysiological actions on VTA neurons in vivo, similar to those produced by ethanol, and significantly participate in ethanol-induced increment in DA neuronal activity. These results also suggest that acetaldehyde, by increasing DA neuronal activity in the VTA, may significantly contribute to the centrally mediated positive motivational properties of ethanol, which would oppose the well-known peripherally originating aversive properties.
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References
Aragon CM, Abitbol M, Amit Z (1986). Acetaldehyde may mediate reinforcement and aversion produced by ethanol. An examination using a conditioned taste-aversion paradigm. Neuropharmacology 25: 79–83.
Aragon CM, Amit Z (1992). The effect of 3-amino-1,2,4-triazole on voluntary ethanol consumption: evidence for brain catalase involvement in the mechanism of action. Neuropharmacology 31: 709–712.
Bailey CP, Manley SJ, Watson WP, Wonnacott S, Molleman A, Little HJ (1998). Chronic ethanol administration alters activity in ventral tegmental area neurons after cessation of withdrawal hyperexcitability. Brain Res 803: 144–152.
Baraona E, Yokoyama A, Ishii H, Hernandez-Munoz R, Takagi T, Tsuchiya M et al (1991). Lack of alcohol dehydrogenase isoenzyme activities in the stomach of Japanese subjects. Life Sci 49: 1929–1934.
Berridge CW, Stratford TL, Foote SL, Kelley AE (1997). Distribution of dopamine beta-hydroxylase-like immunoreactive fibers within the shell subregion of the nucleus accumbens. Synapse 27: 230–241.
Brodie MS, Shefner SA, Dunwiddie TV (1990). Ethanol increases the firing rate of dopamine neurons of the rat ventral tegmental area in vitro. Brain Res 508: 65–69.
Brodie MS, McElvain MA, Bunney EB, Appel SB (1999). Pharmacological reduction of small conductance calcium-activated potassium current (SK) potentiates the excitatory effect of ethanol on ventral tegmental area dopamine neurons. J Pharmacol Exp Ther 290: 325–333.
Brown ZW, Amit Z, Rockman GE (1979). Intraventricular self-administration of acetaldehyde, but not ethanol, in naïve laboratory rats. Psychopharmacology (Berl) 64: 271–276.
Brown ZW, Amit Z, Smith BR (1980). Intraventricular self-administration of acetaldehyde and voluntary consumption of ethanol in rats. Behav Neural Biol 28: 150–155.
Chick J, Gough K, Falkowski W, Kershaw P, Hore B, Mehta B et al (1992). Disulfiram treatment of alcoholism. Br J Psychiatry 161: 84–89.
Cooper DC (2002). The significance of action potential bursting in the brain reward circuit. Neurochem Int 41: 333–340.
Devoto P, Flore G, Pira L, Diana M, Gessa GL (2002). Co-release of noradrenaline and dopamine in the prefrontal cortex after acute morphine and during morphine withdrawal. Psychopharmacology (Berl) 160: 220–224.
Diana M (1996). Dopaminergic neurotransmission and drug withdrawal: relevance to drug craving. In: Ohye C, Kimura M, McKenzie J (eds). The Basal Ganglia V. Advances in Behavioral Biology 47. Plenum Press: New York. pp 123–130.
Diana M (1998). Drugs of abuse and dopamine cell activity. Adv Pharmacol 42: 998–1001.
Diana M, Tepper JM (2002). Electrophysiological pharmacology of mesencephalic dopaminergic neurons. In: G Di Chiara (ed). Handbook of Experimental Pharmacology 154/II. Springer-Verlag: Berlin, Heidelberg. pp 1–62.
Diana M, Garcia-Munoz M, Richards J, Freed CR (1989). Electrophysiological analysis of dopamine cells from the substantia nigra pars compacta of circling rats. Exp Brain Res 74: 625–630.
Diana M, Pistis M, Carboni S, Gessa GL, Rossetti ZL (1993). Profound decrement of mesolimbic dopaminergic neuronal activity during ethanol withdrawal syndrome in rats: electrophysiological and biochemical evidence. Proc Natl Acad Sci USA 90: 7966–7969.
Eriksson CJ (2001). The role of acetaldehyde in the actions of alcohol (update 2000). Alcohol Clin Exp Res 25: 15S–32S; review.
Fadda F, Rossetti ZL (1998). Chronic ethanol consumption: from neuroadaptation to neurodegeneration. Prog Neurobiol 56: 385–431.
Fuller RK, Roth HP (1979). Disulfiram for the treatment of alcoholism. An evaluation in 128 men. Ann Intern Med 90: 901–904.
Gessa GL, Muntoni F, Collu M, Vargiu L, Mereu G (1985). Low doses of ethanol activate dopaminergic neurons in the ventral tegmental area. Brain Res 348: 201–203.
Goodwin DW, Gabrielli WF (1997). Alcohol: clinical aspects. In: Lowinson JH, Ruiz P, Millman RB, Langrod JG (eds). Substance Abuse: A Comprehensive Textbook 3rd edn. Williams & Wilkins: Baltimore, MD. pp 142–148.
Grace AA, Bunney BS (1984). The control of firing pattern in nigral dopamine neurons: burst firing. J Neurosci 4: 2877–2890.
Imperato A, Di Chiara G (1986). Preferential stimulation of dopamine release in the nucleus accumbens of freely moving rats by ethanol. J Pharmacol Exp Ther 239: 219–228.
Litten RZ, Allen J, Fertig J (1996). Pharmacotherapies for alcohol problems: a review of research with focus on developments since 1991. Alcohol Clin Exp Res 20: 859–876.
McBride WJ, Li TK, Deitrich RA, Zimatkin S, Smith BR, Rodd-Henricks ZA (2002). Involvement of acetaldehyde in alcohol addiction. Alcohol Clin Exp Res 26: 114–119.
Mereu G, Fadda F, Gessa GL (1984). Ethanol stimulates the firing rate of nigral dopaminergic neurons in unanesthetized rats. Brain Res 292: 63–69.
Myers WD, Ng KT, Singer G (1982). Intravenous self-administration of acetaldehyde in the rat as a function of schedule, food deprivation and photoperiod. Pharmacol Biochem Behav 17: 807–811.
Myers WD, Ng KT, Singer G (1984). Ethanol preference in rats with a prior history of acetaldehyde self-administration. Experientia 40: 1008–1010.
Overton PG, Clark D (1997). Burst firing in midbrain dopaminergic neurons. Brain Res Rev 25: 312–334.
Paxinos G, Watson C (1997). The Rat Brain in Stereotaxic Coordinates compact 3rd edn Academic Press, New York.
Pulvirenti L, Diana M (2001). Drug dependence as a disorder of neural plasticity: focus on dopamine and glutamate. Rev Neurosci 12: 41–59.
Quertemont E, De Witte P (2001). Conditioned stimulus preference after acetaldehyde but not ethanol injections. Pharmacol Biochem Behav 68: 449–454.
Quertemont E, Escarabajal MD, De Witte P (2003). Role of catalase in ethanol-induced conditioned taste aversion: a study with 3-amino-1,2,4-triazole. Drug Alcohol Depend 70: 77–83.
Rodd-Henricks ZA, Melendez RI, Zaffaroni A, Goldstein A, McBride W, Li TK (2002). The reinforcing effects of acetaldehyde in the posterior ventral tegmental area of alcohol preferring rats. Pharmacol Biochem Behav 72: 55–64.
Rodd-Henricks ZA, McKinzie DL, Crile RS, Murphy JM, McBride WJ (2000). Regional heterogeneity for the intracranial self-administration of ethanol within the ventral tegmental area of female Wistar rats. Psychopharmacology (Berl) 149: 217–224.
Rossetti ZL, Hmaidan Y, Gessa GL (1992). Marked inhibition of mesolimbic dopamine release: a common feature of ethanol, morphine, cocaine and amphetamine abstinence in rats. Eur J Pharmacol 221: 227–234.
Smith BR, Amit Z, Splawinsky J (1984). Conditioned place preference induced by intraventricular infusions of acetaldehyde. Alcohol 1: 193–195.
Tyndale RF, Pianezza ML, Sellers EM (1999). A common genetic defect in nicotine metabolism decreases risk for dependence and lowers cigarette consumption. Nicotine Tob Res 1(Suppl 2): S63-67, discussion S69-70.
Waller MB, McBride WJ, Lumeng L, Li TK (1982). Effects of intravenous ethanol and of 4-methylpyrazole on alcohol drinking in alcohol-preferring rats. Pharmacol Biochem Behav 17: 763–768.
Ward RJ, Colantuoni C, Dahchour A, Quertemont E, De Witte P (1997). Acetaldehyde-induced changes in monoamine and amino acid extracellular microdialysate content of the nucleus accumbens. Neuropharmacology 36: 225–232.
Weiss F, Parsons LH, Schulteis G, Hyytia P, Lorang MT, Bloom FE et al (1996). Ethanol self-administration restores withdrawal-associated deficiencies in accumbal dopamine and 5-hydroxytryptamine release in dependent rats. J Neurosci 16: 3474–3485.
Zimatkin SM, Lindros KO (1996). Distribution of catalase in rat brain: aminergic neurons as possible targets for ethanol effects. Alcohol Alcohol 31: 167–174.
Acknowledgements
This work was supported in part by a grant from MIUR to MD. We thank Delia Macciotta and Daniela Lampis for their expert technical assistance and William Dunn III for proofreading the manuscript.
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Foddai, M., Dosia, G., Spiga, S. et al. Acetaldehyde Increases Dopaminergic Neuronal Activity in the VTA. Neuropsychopharmacol 29, 530–536 (2004). https://doi.org/10.1038/sj.npp.1300326
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DOI: https://doi.org/10.1038/sj.npp.1300326
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