Westphalen R I, Stadlin A
Department of Anatomy, Chinese University of Hong Kong, Shatin, NT.
Ann N Y Acad Sci. 2000 Sep;914:187-93. doi: 10.1111/j.1749-6632.2000.tb05195.x.
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.
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。