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临床神经学中的NMDA受体:兴奋的未来

NMDA receptors in clinical neurology: excitatory times ahead.

作者信息

Kalia Lorraine V, Kalia Suneil K, Salter Michael W

机构信息

Division of Neurology, Department of Medicine, University of Toronto, ON, Canada.

出版信息

Lancet Neurol. 2008 Aug;7(8):742-55. doi: 10.1016/S1474-4422(08)70165-0.

Abstract

Since the N-methyl-D-aspartate receptor (NMDAR) subunits were cloned less than two decades ago, a substantial amount of research has been invested into understanding their physiological function in the healthy CNS. Research has also been directed at their pathological roles in various neurological diseases, including disorders resulting from acute excitotoxic insults (eg, ischaemic stroke, traumatic brain injury), diseases due to chronic neurodegeneration (eg, Alzheimer's, Parkinson's, and Huntington's diseases and amyotrophic lateral sclerosis), disorders arising from sensitisation of neurons (eg, epilepsy, neuropathic pain), and neurodevelopmental disorders associated with NMDAR hypofunction (eg, schizophrenia). Selective NMDAR antagonists have not produced positive results in clinical trials. However, there are other NMDAR-targeted therapies used in current practice that are effective for treating some neurological disorders. In this Review, we describe the evidence for the use of these therapies and provide an overview of drugs being investigated in clinical trials. We also discuss new NMDAR-targeted strategies in clinical neurology.

摘要

自从 N-甲基-D-天冬氨酸受体(NMDAR)亚基在不到二十年前被克隆出来后,大量研究致力于了解它们在健康中枢神经系统中的生理功能。研究还针对它们在各种神经系统疾病中的病理作用,包括急性兴奋毒性损伤导致的疾病(如缺血性中风、创伤性脑损伤)、慢性神经退行性疾病(如阿尔茨海默病、帕金森病、亨廷顿病和肌萎缩侧索硬化症)、神经元敏化引起的疾病(如癫痫、神经性疼痛)以及与 NMDAR 功能减退相关的神经发育障碍(如精神分裂症)。选择性 NMDAR 拮抗剂在临床试验中未产生阳性结果。然而,目前临床实践中使用的其他针对 NMDAR 的疗法对治疗某些神经系统疾病是有效的。在本综述中,我们描述了使用这些疗法的证据,并概述了正在临床试验中研究的药物。我们还讨论了临床神经病学中针对 NMDAR 的新策略。

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