6-OHDA-lesions of the nucleus accumbens disrupt the acquisition but not the maintenance of ethanol consumption in the alcohol-preferring P line of rats
- PMID: 9309315
6-OHDA-lesions of the nucleus accumbens disrupt the acquisition but not the maintenance of ethanol consumption in the alcohol-preferring P line of rats
Abstract
The aim of the present study was to determine whether reduction of dopamine (DA) innervation to the nucleus accumbens (ACB) alters the maintenance and/or acquisition of ethanol drinking in female alcohol-preferring P rats. Compared with sham-lesioned animals, bilateral microinjections of 6-OHDA (12 micrograms/2.4 microliters/site) into the ACB did not alter the consumption of 10% ethanol in rats that had prior experience of ethanol drinking, with both sham- and 6-OHDA-lesioned groups recovering to presurgical consumption levels at similar rates. On the other hand, the identical lesion procedure disrupted the acquisition of ethanol intake in rats with no ethanol-drinking experience prior to the lesions. A sham-lesioned group attained an ethanol intake of approximately 7 g/kg/day in 1 week, which was maintained over the following 2-week period, while the ethanol intake of the 6-OHDA-lesioned group was approximately 60% lower after 1 week and 30% lower at the end of 3 weeks. DA content of the ACB was 60% lower in both groups of the 6-OHDA-treated rats compared with the controls. The results suggest that different neural mechanisms may underlie the acquisition and maintenance of ethanol drinking behavior; the ACB DA system appears to play an important role in the acquisition of ethanol drinking.
Similar articles
-
Naltrexone suppresses ethanol intake in 6-hydroxydopamine-treated rats.Alcohol Clin Exp Res. 2001 Nov;25(11):1605-12. Alcohol Clin Exp Res. 2001. PMID: 11707635
-
Ethanol drinking experience attenuates (-)sulpiride-induced increases in extracellular dopamine levels in the nucleus accumbens of alcohol-preferring (P) rats.Alcohol Clin Exp Res. 2003 Mar;27(3):424-31. doi: 10.1097/01.ALC.0000056618.57931.A5. Alcohol Clin Exp Res. 2003. PMID: 12658107
-
Reverse microdialysis of a dopamine uptake inhibitor in the nucleus accumbens of alcohol-preferring rats: effects on dialysate dopamine levels and ethanol intake.Alcohol Clin Exp Res. 2000 Jun;24(6):795-801. Alcohol Clin Exp Res. 2000. PMID: 10888067
-
Microinjection of sulpiride into the nucleus accumbens increases ethanol drinking in alcohol-preferring (P) rats.Alcohol Alcohol Suppl. 1991;1:417-20. Alcohol Alcohol Suppl. 1991. PMID: 1845571
-
Serotonin, dopamine and GABA involvement in alcohol drinking of selectively bred rats.Alcohol. 1990 May-Jun;7(3):199-205. doi: 10.1016/0741-8329(90)90005-w. Alcohol. 1990. PMID: 2184832 Review.
Cited by
-
Serotonin-3 receptors in the posterior ventral tegmental area regulate ethanol self-administration of alcohol-preferring (P) rats.Alcohol. 2010 May;44(3):245-55. doi: 10.1016/j.alcohol.2010.01.002. Alcohol. 2010. PMID: 20682192 Free PMC article.
-
Long-lasting potentiation of GABAergic synapses in dopamine neurons after a single in vivo ethanol exposure.J Neurosci. 2002 Mar 15;22(6):2074-82. doi: 10.1523/JNEUROSCI.22-06-02074.2002. J Neurosci. 2002. PMID: 11896147 Free PMC article.
-
Kappa-opioid receptor modulation of accumbal dopamine concentration during operant ethanol self-administration.Neuropharmacology. 2006 Sep;51(3):487-96. doi: 10.1016/j.neuropharm.2006.04.005. Epub 2006 Jun 15. Neuropharmacology. 2006. PMID: 16781738 Free PMC article.
-
Influence of the endogenous opioid system on high alcohol consumption and genetic predisposition to alcoholism.J Psychiatry Neurosci. 2001 Sep;26(4):304-18. J Psychiatry Neurosci. 2001. PMID: 11590970 Free PMC article. Review.
-
Greater ethanol inhibition of presynaptic dopamine release in C57BL/6J than DBA/2J mice: Role of nicotinic acetylcholine receptors.Neuroscience. 2015 Jan 22;284:854-864. doi: 10.1016/j.neuroscience.2014.10.052. Epub 2014 Nov 4. Neuroscience. 2015. PMID: 25451295 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical