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静脉麻醉药与脑保护受体机制
引用本文:王莉,金正均,杭燕南. 静脉麻醉药与脑保护受体机制[J]. 上海交通大学学报(医学版), 2004, 24(11): 978-980
作者姓名:王莉  金正均  杭燕南
作者单位:[1]上海交通大学第六人民医院麻醉科,上海200233 [2]上海第二医科大学基础医学院药理教研室,上海200233 [3]上海第二医科大学仁济医院麻醉科,上海200233
摘    要:兴奋毒性可能是造成神经元死亡的“最后公路”。已知静脉麻醉药,如非竞争性NMDA受体拮抗刹(氯胺酮)和GABA受体模拟剂(丙泊酚)有神经保护作用,该文就它们的神经保护作用的受体机制研究加以综述。

关 键 词:静脉麻醉药  脑保护  受体机制  兴奋性氨基酸
文章编号:0258-5898(2004)11-0978-03
修稿时间:2004-04-11

Intravenous anesthetics and the receptor mechanism of neuroprotection
WANG Li reviewer,JIN Zheng-jun,HANG Yan-nan revisers. Intravenous anesthetics and the receptor mechanism of neuroprotection[J]. Journal of Shanghai Jiaotong University:Medical Science, 2004, 24(11): 978-980
Authors:WANG Li reviewer  JIN Zheng-jun  HANG Yan-nan revisers
Abstract:The excitotoxicity may be the last public way by which neurons were led to death. It has been shown that intravenous anesthetics, such as non-competitive NMDA antagonists (ketamine) or GABAmimetics (propofol) have neuroprotection. The receptor mechanism of neuroprotection by intravenous anesthesia was reviewed in this essay.
Keywords:excitatory amino acid  NMDA  brain protection  intravenous anesthetics
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