拟精神病
苯环己定
NMDA受体
药理学
神经毒性
氯胺酮
神经保护
谷氨酸受体
地唑西平
神经科学
医学
敌手
机制(生物学)
安定
化学
麻醉
受体
生物
毒性
内科学
哲学
认识论
作者
John W. Olney,Joann Labruyere,G. Wang,David F. Wozniak,Madelon T. Price,Michael A. Sesma
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1991-12-06
卷期号:254 (5037): 1515-1518
被引量:842
标识
DOI:10.1126/science.1835799
摘要
Antagonists of the N -methyl-D-aspartate (NMDA) subtype of glutamate receptor, including phencyclidine (PCP) and ketamine, protect against brain damage in neurological disorders such as stroke. However, these agents have psychotomimetic properties in humans and morphologically damage neurons in the cerebral cortex of rats. It is now shown that the morphological damage can be prevented by certain anticholinergic drugs or by diazepam and barbiturates, which act at the γ-aminobutyric acid (GABA) receptor-channel complex and are known to suppress the psychotomimetic symptoms caused by ketamine. Thus, it may be possible to prevent the unwanted side effects of NMDA antagonists, thereby enhancing their utility as neuroprotective drugs.
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