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钠敏感型可卡因与大鼠纹状体膜的结合:与多巴胺摄取位点的可能关系。

Sodium-sensitive cocaine binding to rat striatal membrane: possible relationship to dopamine uptake sites.

作者信息

Kennedy L T, Hanbauer I

出版信息

J Neurochem. 1983 Jul;41(1):172-8. doi: 10.1111/j.1471-4159.1983.tb13666.x.

Abstract

In rat striatal membranes, NaCl induced a twofold increase in the maximal number of cocaine binding sites but did not alter the affinity of these sites for cocaine. This effect was concentration-dependent, specific to sodium ions, and occurred in membranes prepared from corpus striatum but not from other brain regions. Lesions with 6-hydroxydopamine but not with kainic acid eliminated the sodium-induced increase in binding and produced a decrease in the Bmax of binding measured in the presence of NaCl. The capacity of a series of drugs to interfere with Na+-dependent cocaine binding correlated well with their capacity to inhibit [3H]dopamine uptake into rat striatal synaptosomes. The present results suggest that Na+-dependent cocaine binding sites are localized presynaptically on dopaminergic nerve terminals in corpus striatum, and may be related to dopamine uptake sites.

摘要

在大鼠纹状体膜中,氯化钠使可卡因结合位点的最大数量增加了两倍,但并未改变这些位点对可卡因的亲和力。这种效应具有浓度依赖性,对钠离子具有特异性,且发生在从纹状体而非其他脑区制备的膜中。用6-羟基多巴胺而非 kainic 酸进行损伤消除了钠诱导的结合增加,并导致在存在氯化钠的情况下测得的结合Bmax降低。一系列药物干扰钠依赖性可卡因结合的能力与其抑制[3H]多巴胺摄取到大鼠纹状体突触体中的能力密切相关。目前的结果表明,钠依赖性可卡因结合位点位于纹状体中多巴胺能神经末梢的突触前,并且可能与多巴胺摄取位点有关。

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