Weiss F, Lorang M T, Bloom F E, Koob G F
Department of Neuropharmacology, Scripps Research Institute, La Jolla, California.
J Pharmacol Exp Ther. 1993 Oct;267(1):250-8.
Dopaminergic neurotransmission in the nucleus accumbens may be an important factor in ethanol reinforcement and genetically determined ethanol preference. This hypothesis was tested by measuring dopamine (DA) release by intracranial microdialysis during voluntary oral ethanol self-administration in alcohol-preferring (P) and genetically heterogeneous Wistar rats. The animals were trained to respond for ethanol (10% w/v) or water in a free-choice operant task. Extracellular DA levels in the nucleus accumbens were subsequently monitored during 30-min self-administration sessions and a 15-min "waiting period" before session onset. Ethanol self-administration in all animals was followed by a significant, dose-dependent rise in DA release with maximal effects at approximately 15 min after peak intake. Dose-effect functions revealed significantly steeper slopes for the DA-releasing effects of ethanol in P than in genetically heterogeneous Wistar rats. Over an identical range of ethanol doses and blood alcohol levels, increases in DA efflux ranged from 143% to 459% of basal levels in P rats but only from 142% to 212% in Wistar rats. To differentiate the pharmacological effects of ethanol from the effects of operant responding, additional groups of P and Wistar rats were tested during self-administration of saccharin (0.05% w/v). By contrast with ethanol, saccharin did not substantially elevate extracellular DA levels. A significant, transient increase in DA efflux was, however, observed in both strains of rats during the presession waiting period in the absence of ethanol or saccharin availability.(ABSTRACT TRUNCATED AT 250 WORDS)
伏隔核中的多巴胺能神经传递可能是乙醇强化作用以及基因决定的乙醇偏好中的一个重要因素。通过在酒精偏好(P)大鼠和基因异质性的Wistar大鼠自愿经口自我摄入乙醇期间,采用颅内微透析法测量多巴胺(DA)释放,对这一假说进行了验证。这些动物接受训练,在自由选择的操作性任务中对乙醇(10% w/v)或水做出反应。随后,在30分钟的自我摄入时段以及时段开始前15分钟的“等待期”内,监测伏隔核中的细胞外DA水平。所有动物自我摄入乙醇后,DA释放均出现显著的、剂量依赖性升高,在摄入量峰值后约15分钟时达到最大效应。剂量效应函数显示,与基因异质性的Wistar大鼠相比,乙醇对P大鼠的DA释放效应的斜率显著更陡。在相同的乙醇剂量和血液酒精水平范围内,P大鼠的DA流出量增加幅度为基础水平的143%至459%,而Wistar大鼠仅为142%至212%。为了区分乙醇的药理作用与操作性反应的作用,在另外几组P大鼠和Wistar大鼠自我摄入糖精(0.05% w/v)期间进行了测试。与乙醇不同,糖精并未显著提高细胞外DA水平。然而,在没有乙醇或糖精供应的情况下,在两个品系的大鼠的时段前等待期内,均观察到DA流出量有显著的短暂增加。(摘要截短于250字)