Rodd Zachary A, Bell Richard L, McQueen Victoria K, Davids Michelle R, Hsu Cathleen C, Murphy James M, Li Ting-Kai, Lumeng Lawrence, McBride William J
Institute of Psychiatric Research, Department of Psychiatry, Indiana University School of Medicine, Indianapolis, 46202, USA.
J Pharmacol Exp Ther. 2005 Nov;315(2):648-57. doi: 10.1124/jpet.105.084350. Epub 2005 Aug 2.
The posterior ventral tegmental area (VTA) is a neuroanatomical substrate mediating the reinforcing effects of ethanol in rats. Repeated alcohol deprivations produce robust ethanol intakes of alcohol-preferring (P) rats during relapse and increase the reinforcing effects of oral alcohol self-administration. The objective of this study was to test the hypothesis that alcohol drinking and repeated alcohol deprivations will increase the reinforcing effects of ethanol within the posterior VTA of P rats. Groups of female P rats were used (alcohol-naive, continuous access, and repeatedly deprived). Each rat was implanted with a guide cannula aimed at the posterior VTA. Depression of the active lever produced the infusion of 100 nl of artificial cerebrospinal fluid (CSF) or ethanol (25-300 mg%). Each rat was given only one ethanol concentration during the 4-h sessions conducted every other day. Compared with the infusions of artificial CSF, the alcohol-naive group reliably self-infused 75 and 150 mg% ethanol, but not the lower or higher concentrations. On the other hand, the continuous access group had significantly higher self-infusions of 50, 75, 150, and 300 mg% ethanol compared with artificial CSF infusions. The repeatedly deprived group also self-infused significantly more of 50, 75, 150, and 300 mg% ethanol than artificial CSF; moreover, the number of infusions for all four concentrations was higher in the repeatedly deprived versus the continuous access group. Chronic alcohol drinking by P rats increased the reinforcing effects of ethanol within the posterior VTA, and repeated alcohol deprivations produced a further increase in these reinforcing effects of ethanol.
腹侧被盖区后部(VTA)是介导乙醇对大鼠强化作用的神经解剖学底物。反复戒酒会使嗜酒(P)大鼠在复发期间大量摄入乙醇,并增强口服乙醇自我给药的强化作用。本研究的目的是检验以下假设:饮酒和反复戒酒会增强P大鼠腹侧被盖区后部乙醇的强化作用。使用了几组雌性P大鼠(未接触过酒精、持续接触酒精和反复戒酒)。每只大鼠都植入了一根瞄准腹侧被盖区后部的引导套管。按压活动杠杆会注入100 nl的人工脑脊液(CSF)或乙醇(25 - 300 mg%)。在每隔一天进行的4小时实验中,每只大鼠只接受一种乙醇浓度。与注入人工脑脊液相比,未接触过酒精的组可靠地自我注入了75和150 mg%的乙醇,但没有注入较低或较高浓度的乙醇。另一方面,持续接触酒精的组与注入人工脑脊液相比,自我注入50、75、150和300 mg%乙醇的量显著更高。反复戒酒的组自我注入50、75、150和300 mg%乙醇的量也显著高于人工脑脊液;此外,与持续接触酒精的组相比,反复戒酒的组对所有四种浓度乙醇的注入次数都更多。P大鼠长期饮酒增强了腹侧被盖区后部乙醇的强化作用,而反复戒酒则使乙醇的这些强化作用进一步增强。