代谢型谷氨酸受体转运及其在药物诱导的神经行为可塑性中的作用。

Peter U Hámor, Marek Schwendt
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引用次数: 0

摘要

谷氨酸是哺乳动物中枢神经系统中的主要兴奋性神经递质,通过统称为神经行为可塑性的过程,指导许多细胞底物和脑回路的发育和体验依赖性变化。谷氨酸受体的细胞表面表达和膜运输的调节是确保最佳兴奋性传递的重要机制,同时也允许微调神经元对谷氨酸的反应。另一方面,越来越多的证据表明,谷氨酸受体运输失调与几种神经精神疾病的病理生理学有关。这篇综述提供了关于啮齿类动物和人脑中调节代谢型谷氨酸(mGlu)受体运输和表面表达的分子决定簇的最新信息,并讨论了mGluR运输在成瘾药物产生的适应不良突触可塑性中的作用。由于大量证据将谷氨酸能功能障碍与毒瘾的进展和严重程度联系在一起,我们对mGluR贩运的理解进展可能为开发成瘾和其他神经精神障碍的新药物疗法提供机会。
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Metabotropic Glutamate Receptor Trafficking and its Role in Drug-Induced Neurobehavioral Plasticity.
Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system that guides developmental and experience-dependent changes in many cellular substrates and brain circuits, through the process collectively referred to as neurobehavioral plasticity. Regulation of cell surface expression and membrane trafficking of glutamate receptors represents an important mechanism that assures optimal excitatory transmission, and at the same time, also allows for fine-tuning neuronal responses to glutamate. On the other hand, there is growing evidence implicating dysregulated glutamate receptor trafficking in the pathophysiology of several neuropsychiatric disorders. This review provides up-to-date information on the molecular determinants regulating trafficking and surface expression of metabotropic glutamate (mGlu) receptors in the rodent and human brain and discusses the role of mGluR trafficking in maladaptive synaptic plasticity produced by addictive drugs. As substantial evidence links glutamatergic dysfunction to the progression and the severity of drug addiction, advances in our understanding of mGluR trafficking may provide opportunities for the development of novel pharmacotherapies of addiction and other neuropsychiatric disorders.
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