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Ketamine's antidepressant action: beyond NMDA receptor inhibition

机译:氯胺酮的抗抑郁作用:超越NMDA受体抑制

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摘要

The N-methyl-D-aspartate (NMDA) receptor antagonist ketamine is one of the most attractive antidepressants since this drug causes rapid-onset and sustained antidepressant effects in treatment resistant patients with depression. There are unanswered questions about how ketamine induces its rapid and sustained antidepressant actions. This key article suggests that (2R,6R)-HNK (hydroxynorketamine), a major metabolite of (R)-ketamine, shows antidepressant effects in rodent models of depression, indicating that the metabolism of (R)-ketamine to (2R,6R)-HNK is pivotal in its antidepressant action. Here these findings are put into context and their significance is discussed.
机译:N-甲基-D-天冬氨酸盐(NMDA)受体拮抗剂氯胺酮是最有吸引力的抗抑郁药之一,因为该药物在治疗性抑郁症患者中引起快速发作和持续的抗抑郁作用。关于氯胺酮如何诱导其快速和持续的抗抑郁作用,尚无答案。该关键文章建议(2R,6R)-HNK(羟基降甲胺酮)是(R)-氯胺酮的主要代谢产物,在啮齿动物抑郁模型中显示出抗抑郁作用,表明(R)-氯胺酮代谢为(2R,6R )-HNK在其抗抑郁作用中起着关键作用。在这里,将这些发现放到上下文中并对其意义进行讨论。

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