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神经疾病中兴奋性毒性的机制。

Mechanisms of excitotoxicity in neurologic diseases.

作者信息

Beal M F

机构信息

Neurochemistry Laboratory, Massachusetts General Hospital, Boston.

出版信息

FASEB J. 1992 Dec;6(15):3338-44.

PMID:1464368
Abstract

Excitotoxicity refers to neuronal cell death caused by activation of excitatory amino acid receptors. A substantial body of evidence has implicated excitotoxicity as a mechanism of cell death in both acute and chronic neurologic diseases. A major recent advance has been the successful cloning and expression of the N-methyl-D-aspartate (NMDA), non-NMDA, and metabotropic glutamate receptors. The cellular mechanisms responsible for cell death after activation of these receptors are still being clarified. In acute neurologic diseases such as stroke and head trauma, excitotoxicity may be related to excessive glutamate release. In chronic neurodegenerative diseases, however, a slow excitotoxic process is more likely to occur as a consequence of either a receptor abnormality or an impairment of energy metabolism. Recent therapeutic studies have demonstrated the efficacy of non-NMDA receptor antagonists in experimental studies of global ischemia.

摘要

兴奋毒性是指由兴奋性氨基酸受体激活所导致的神经元细胞死亡。大量证据表明,兴奋毒性在急性和慢性神经疾病中均为细胞死亡的一种机制。近期的一项重大进展是成功克隆并表达了N-甲基-D-天冬氨酸(NMDA)受体、非NMDA受体和代谢型谷氨酸受体。这些受体激活后导致细胞死亡的细胞机制仍在阐明之中。在诸如中风和头部创伤等急性神经疾病中,兴奋毒性可能与谷氨酸过度释放有关。然而,在慢性神经退行性疾病中,由于受体异常或能量代谢受损,更有可能发生缓慢的兴奋毒性过程。近期的治疗研究已证明非NMDA受体拮抗剂在全脑缺血实验研究中的疗效。

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