Gedeon Richter Plc., Pharmacological and Drug Safety Research, Laboratory for Molecular Cell Biology, Budapest 10. P.O. Box 27, H-1475 Hungary.
Curr Neuropharmacol. 2008 Mar;6(1):39-54. doi: 10.2174/157015908783769662.
Long-term alcohol exposure may lead to development of alcohol dependence in consequence of altered neurotransmitter functions. Accumulating evidence suggests that the N-methyl-D-aspartate (NMDA) type of glutamate receptors is a particularly important site of ethanol's action. Several studies showed that ethanol potently inhibits NMDA receptors (NMDARs) and prolonged ethanol exposition leads to a compensatory "up-regulation" of NMDAR mediated functions. Therefore, alterations in NMDAR function are supposed to contribute to the development of ethanol tolerance, dependence as well as to the acute and late signs of ethanol withdrawal.A number of publications report alterations in the expression and phosphorylation states of NMDAR subunits, in their interaction with scaffolding proteins or other receptors in consequence of chronic ethanol treatment. Our knowledge on the regulatory processes, which modulate NMDAR functions including factors altering transcription, protein expression and post-translational modifications of NMDAR subunits, as well as those influencing their interactions with different regulatory proteins or other downstream signaling elements are incessantly increasing. The aim of this review is to summarize the complex chain of events supposedly playing a role in the up-regulation of NMDAR functions in consequence of chronic ethanol exposure.
长期饮酒可能会导致神经递质功能改变,进而发展为酒精依赖。越来越多的证据表明,N-甲基-D-天冬氨酸(NMDA)型谷氨酸受体是乙醇作用的一个特别重要的位点。多项研究表明,乙醇能强烈抑制 NMDA 受体(NMDARs),而长期乙醇暴露会导致 NMDAR 介导的功能代偿性“上调”。因此,NMDAR 功能的改变可能有助于乙醇耐受、依赖的发展,以及乙醇戒断的急性和晚期症状。许多出版物报道了 NMDAR 亚基表达和磷酸化状态的改变,以及它们与支架蛋白或其他受体的相互作用,这些都是由于慢性乙醇处理所致。我们对调节 NMDAR 功能的调控过程的认识不断增加,包括改变转录、蛋白质表达和 NMDAR 亚基翻译后修饰的因素,以及影响它们与不同调节蛋白或其他下游信号转导元件相互作用的因素。本文综述的目的是总结慢性乙醇暴露导致 NMDAR 功能上调的复杂事件链。