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多巴胺摄取阻滞剂可消除甲基苯丙胺引起的大鼠纹状体突触体中多巴胺摄取及质膜电位的降低。

Dopamine uptake blockers nullify methamphetamine-induced decrease in dopamine uptake and plasma membrane potential in rat striatal synaptosomes.

作者信息

Westphalen R I, Stadlin A

机构信息

Department of Anatomy, Chinese University of Hong Kong, Shatin, NT.

出版信息

Ann N Y Acad Sci. 2000 Sep;914:187-93. doi: 10.1111/j.1749-6632.2000.tb05195.x.

Abstract

Rat striatal synaptosomes showed a reduced capacity to generate a membrane potential after being exposed to methamphetamine (METH) for 1 h. As a consequence, the dopamine (DA) synaptosomes were impeded in their electrogenic-dependent reuptake of dopamine. The capacity for METH-exposed nerve terminals to generate a membrane potential may contribute to the ability of METH to destroy dopaminergic neurons. DA uptake inhibitors (DAUIs) were found to counteract the METH-induced decrease in synaptosomal [3H]DA Vmax by stablizing METH-induced reductions in PMP. Because DAUIs showed the same effects as a Na+-channel blocker, DAUIs may prevent METH-induced destruction of dopaminergic neurons by raising plasma membrane potential.

摘要

大鼠纹状体突触体在暴露于甲基苯丙胺(METH)1小时后,产生膜电位的能力降低。因此,多巴胺(DA)突触体对多巴胺的电生性依赖性再摄取受到阻碍。暴露于METH的神经末梢产生膜电位的能力可能有助于METH破坏多巴胺能神经元的能力。发现多巴胺摄取抑制剂(DAUIs)通过稳定METH诱导的PMP降低来抵消METH诱导的突触体[3H]DA Vmax的降低。由于DAUIs显示出与钠通道阻滞剂相同的作用,DAUIs可能通过提高质膜电位来防止METH诱导的多巴胺能神经元破坏。

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