Becker H C, Jarvis M F
Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, 29425 USA.
Eur J Pharmacol. 1996 Jan 18;296(1):43-6. doi: 10.1016/0014-2999(95)00766-0.
The effect of chronic ethanol exposure and withdrawal on [3H]RO15-4513 (ethyl-8-azido-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5a][1,4] benzodiazepine-3-carboxylate) binding to diazepam-sensitive and diazepam-insensitive binding sites was determined in mouse brain. Neither chronic ethanol treatment nor withdrawal significantly altered total [3H]RO15-4513 binding in mouse cortex or cerebellum. However, diazepam-insensitive [3H]RO15-4513 binding density (Bmax) in cerebellum was significantly increased immediately following chronic ethanol treatment (60%) and at 8 h following withdrawal (75%). [3H]RO15-4513 binding affinity was not significantly influenced by chronic ethanol exposure or withdrawal. These results indicate that chronic ethanol treatment and withdrawal can selectively up-regulate diazepam-insensitive [3H]RO15-4513 binding sites and suggest that this unique GABAA receptor subtype may play some role in ethanol dependence and withdrawal.
在小鼠大脑中测定了慢性乙醇暴露和戒断对[3H]RO15 - 4513(8 - 叠氮基 - 5,6 - 二氢 - 5 - 甲基 - 6 - 氧代 - 4H - 咪唑并[1,5a][1,4]苯二氮䓬 - 3 - 羧酸乙酯)与地西泮敏感和地西泮不敏感结合位点结合的影响。慢性乙醇处理和戒断均未显著改变小鼠皮质或小脑中[3H]RO15 - 4513的总结合。然而,慢性乙醇处理后立即(增加60%)以及戒断后8小时(增加75%),小脑中地西泮不敏感的[3H]RO15 - 4513结合密度(Bmax)显著增加。[3H]RO15 - 4513的结合亲和力未受到慢性乙醇暴露或戒断的显著影响。这些结果表明,慢性乙醇处理和戒断可选择性地上调地西泮不敏感的[3H]RO15 - 4513结合位点,并提示这种独特的GABAA受体亚型可能在乙醇依赖和戒断中发挥某些作用。