Alburges M E, Narang N, Wamsley J K
Department of Pharmaceutical Sciences, North Dakota State University, Fargo 58105.
Synapse. 1993 Aug;14(4):314-23. doi: 10.1002/syn.890140409.
Several studies suggest that one of the most important factors contributing to cocaine dependence is an alteration in the actions of the neurotransmitter dopamine in the central nervous system. In order to understand some of the neuroreceptor consequences of cocaine administration, groups of rats were injected with cocaine (2 daily doses of 15 mg/kg) for 1 to 21 days. Binding of [3H]cocaine, [3H]SCH23390, [3H]raclopride, and [3H]BTCP in striatal and cortical tissue from the treated animals was compared to controls. [3H]Cocaine binding was increased by the drug in the striatum and cortex at days 14 and 21, respectively. The binding of [3H]SCH23390 to D1 dopamine receptors was significantly increased at day 3 of cocaine exposure. In striatal membranes, [3H]BTCP binding to dopamine uptake sites was significantly increased after day 7, whereas binding in cortical membranes was increased from day 1. [3H]Raclopride binding to D2 dopamine receptors remained unchanged throughout the study in both cortical and striatal tissues. These results indicate that repeated exposure to cocaine produces an upregulation (possible supersensitivity) in cortical D1, cocaine, and DA-uptake sites which occurs in a time-dependent manner. These increases are coupled with an upregulation in striatal D1, cocaine, and DA-uptake sites, without simultaneous changes in D2 receptors. Thus, cocaine's effects are not uniformly distributed across all brain regions, but rather are focused within areas of the dopamine system.
多项研究表明,导致可卡因成瘾的最重要因素之一是中枢神经系统中神经递质多巴胺作用的改变。为了了解可卡因给药的一些神经受体后果,给几组大鼠注射可卡因(每天2次,每次剂量为15mg/kg),持续1至21天。将处理过的动物纹状体和皮质组织中[3H]可卡因、[3H]SCH23390、[3H]雷氯必利和[3H]BTCP的结合情况与对照组进行比较。在第14天和第21天,药物分别使纹状体和皮质中的[3H]可卡因结合增加。在可卡因暴露第3天时,[3H]SCH23390与D1多巴胺受体的结合显著增加。在纹状体膜中,第7天后[3H]BTCP与多巴胺摄取位点的结合显著增加,而在皮质膜中,从第1天开始结合增加。在整个研究过程中,皮质和纹状体组织中[3H]雷氯必利与D2多巴胺受体的结合均保持不变。这些结果表明,反复接触可卡因会导致皮质D1、可卡因和多巴胺摄取位点上调(可能是超敏反应),且这种上调呈时间依赖性。这些增加与纹状体D1、可卡因和多巴胺摄取位点的上调相关,而D2受体没有同时发生变化。因此,可卡因的作用并非均匀分布于所有脑区,而是集中在多巴胺系统的区域内。