氯胺酮作为速效抗抑郁药的出现:机制见解和未来方向

Atamjit Singh, P. Bedi
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引用次数: 0

摘要

氯胺酮是苯环利定衍生物和n -甲基- d -天冬氨酸受体拮抗剂,作为解离麻醉剂广泛使用。由于其相关的副作用和更新、更安全的麻醉药的出现,它作为人类麻醉剂的使用逐渐减少。近几十年来,有关其治疗具有抗自杀潜力的顽固性抑郁症的疗效的各种报道引起了全球研究人员的极大关注。与传统抗抑郁药需要数周时间相比,氯胺酮在数小时内就能迅速产生临床效果,这使其成为抗抑郁药研究的热门话题。近年来的研究表明,其作用机制是通过NMDA、AMPA等受体调节谷氨酸,下调BDNF等。本章将阐明氯胺酮与抗抑郁活性相关的各种机制。同时还将讨论其药代动力学、毒理学和正在进行的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of Ketamine as a Rapid Acting Antidepressant: Mechanistic Insights and Future Directions
Ketamine is a phencyclidine derivative and N-methyl-D-aspartate receptor antagonist, widely popular as a dissociative anesthetic. Its use as an anesthetic in humans was progressively fallen out due to its associated adverse effects and the emergence of newer and safer anesthetics. In recent few decades, various reports related to its efficacy in the treatment of resistant depression with anti-suicidal potential draw significant attention from researchers around the globe. The rapid clinical effect of ketamine within hours as compared to traditional antidepressants that take several weeks makes it a hot topic in antidepressant research. Studies conducted in the recent past suggest its mechanism of action through glutamate modulation via receptors like NMDA, AMPA as well as downregulation of BDNF etc. This chapter will shed light on the various mechanisms of ketamine related to antidepressant activity. Along with that its pharmacokinetics, toxicology and ongoing clinical trials will also be discussed.
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