拟精神病
NMDA受体
γ-氨基丁酸受体
异氟醚
药理学
神经保护
神经毒性
氯胺酮
苯环己定
受体拮抗剂
化学
美金刚
氟烷
敌手
受体
神经科学
医学
麻醉
生物
毒性
内科学
生物化学
作者
Shinichi Nakao,Atsushi Nagata,Munehiro Masuzawa,Etsuko Miyamoto,Makiko Yamada,Nobuyasu Nishizawa,Koh Shingu
出处
期刊:PubMed
日期:2003-06-01
卷期号:52 (6): 594-602
被引量:7
摘要
Non-competitive NMDA receptor antagonists, in spite of their neuroprotective effects against neuronal ischemia, brain trauma, etc., cause neuronal damage in the rodent posterior cingulate and retrosplenial cortices (PC/RS), which are thought to be responsible brain regions for their psychotomimetic activity in humans. A number of anesthetics have not only GABAA receptor activating properties but also NMDA receptor antagonist properties. On the other hand, ketamine and nitrous oxide, both of which are potent non-competitive NMDA receptor antagonists and have little GABAA activating properties, are demonstrated to induce neuronal damage in the rat PC/RS. Furthermore, ketamine potentiates the neuronal damage by nitrous oxide. Although many anesthetics, such as halothane, isoflurane, barbiturates and benzodiazepines, inhibit the neuronal damage in the PC/RS by NMDA receptor antagonists, probably through GABAA receptor activation, we anesthesiologists should be aware of the risk of ketamine or nitrous oxide anesthesia, not to speak of the combined use of them, without using GABAA receptor activating agents.
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