Nakao Shinichi, Nagata Atsushi, Masuzawa Munehiro, Miyamoto Etsuko, Yamada Makiko, Nishizawa Nobuyasu, Shingu Koh
Department of Anesthesiology, Kansai Medical University, Moriguchi 570-8507.
Masui. 2003 Jun;52(6):594-602.
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.
非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂尽管对神经元缺血、脑外伤等具有神经保护作用,但会导致啮齿动物后扣带回和压后皮质(PC/RS)的神经元损伤,而这些脑区被认为是其在人类中产生拟精神病活性的责任脑区。许多麻醉剂不仅具有GABAA受体激活特性,还具有NMDA受体拮抗剂特性。另一方面,氯胺酮和一氧化二氮都是强效的非竞争性NMDA受体拮抗剂,且几乎没有GABAA激活特性,已被证明会在大鼠PC/RS中诱导神经元损伤。此外,氯胺酮会增强一氧化二氮对神经元的损伤作用。尽管许多麻醉剂,如氟烷、异氟烷、巴比妥类药物和苯二氮䓬类药物,可能通过激活GABAA受体抑制NMDA受体拮抗剂对PC/RS的神经元损伤,但我们麻醉医生应该意识到氯胺酮或一氧化二氮麻醉的风险,更不用说它们的联合使用了,除非使用GABAA受体激活剂。