Serotonin-3 receptor and ethanol-stimulated somatodendritic dopamine release

被引:100
作者
Campbell, AD
Kohl, RR
McBride, WJ
机构
[1] INDIANA UNIV,SCH MED,INST PSYCHIAT RES,INDIANAPOLIS,IN 46202
[2] INDIANA UNIV,SCH MED,DEPT PSYCHIAT,INDIANAPOLIS,IN 46202
[3] INDIANA UNIV,SCH MED,DEPT BIOCHEM,INDIANAPOLIS,IN 46202
[4] PROGRAM MED NEUROBIOL,INDIANAPOLIS,IN 46202
关键词
serotonin-9; receptor; somatodendritic dopamine release; ventral tegmental area; ICS; 205-930; 1-(m-chlorophenyl)-biguanide; in vivo microdialysis; ethanol-stimulated dopamine release;
D O I
10.1016/S0741-8329(96)00069-9
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
The effects of local application of the 5-HT3 receptor agonist, 1-(m-chlorophenyl)-biguanide (CPBG), and IP administration of ethanol on the extracellular levels of dopamine (DA) in the ventral tegmental area (VTA) were studied using in vivo microdialysis. Adult female Wistar rats were implanted with microdialysis probes in the VTA at least 24 h before each experiment. Stable extracellular levels of DA (101 +/- 9 fmol/20 min) were established before initiating the experiments. Application of 10-250 mu M CPBG through the microdialysis probe dose-dependently enhanced the extracellular concentrations of DA but did not alter the levels of either 3,4-dihydroxyphenylacetic acid or homovanillic acid in the dialysate. The effects of CPBG were reversible and dependent upon Ca2+. Co-perfusion with the 5-HT3 receptor antagonist, 3-tropanyl-indole-3-carboxylate (ICS 205-930), inhibited the effects of CPBG on enhancing extracellular DA levels. The IP administration of 2 g/kg ethanol significantly (p < 0.005) enhanced the levels of DA to 150% of baseline values; this ethanol-induced increase was prevented by local perfusion with 100 mu M ICS 205-930. These results suggest that 5-HT3 receptors in the VTA are involved in regulating the somatodendritic release of DA and in mediating the stimulatory effects of ethanol on this neuronal system. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:569 / 574
页数:6
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