Strasburger S E, Bhimani P M, Kaabe J H, Krysiak J T, Nanchanatt D L, Nguyen T N, Pough K A, Prince T A, Ramsey N S, Savsani K H, Scandlen L, Cavaretta M J, Raffa R B
Temple University School of Pharmacy, Philadelphia, PA, USA.
University of Arizona College of Pharmacy, Tucson, AZ, USA.
J Clin Pharm Ther. 2017 Apr;42(2):147-154. doi: 10.1111/jcpt.12497. Epub 2017 Jan 22.
Abundant clinical data now confirm that ketamine produces a remarkable rapid-onset antidepressant effect - hours or days - in contrast to the delayed onset (typically weeks) of current antidepressant drugs. This surprising and revolutionary finding may lead to the development of life-saving pharmacotherapy for depressive illness by reducing the high suicide risk associated with the delayed onset of effect of current drugs. As ketamine has serious self-limiting drawbacks that restrict its widespread use for this purpose, a safer alternative is needed. Our objective is to review the proposed mechanism(s) of ketamine's rapid-onset antidepressant action for new insights into the physiological basis of depressive illness that may lead to new and novel targets for antidepressant drug discovery.
A search was conducted on published literature (e.g. PubMed) and Internet sources to identify information relevant to ketamine's rapid-acting antidepressant action and, specifically, to the possible mechanism(s) of this action. Key search words included 'ketamine', 'antidepressant', 'mechanism of action', 'depression' and 'rapid acting', either individually or in combination. Information was sought that would include less well-known, as well as well-known, basic pharmacologic properties of ketamine and that identified and evaluated the several hypotheses about ketamine's mechanism of antidepressant action.
Whether the mechanistic explanation for ketamine's rapid-onset antidepressant action is related to its well-known antagonism of the NMDA (N-Methyl-d-aspartate) subtype of glutamate receptor or to something else has not yet been fully elucidated. The evidence from pharmacologic, medicinal chemistry, animal model and drug-discovery sources reveals a wide variety of postulated mechanisms.
The surprising discovery of ketamine's rapid-onset antidepressant effect is a game-changer for the understanding and treatment of depressive illness. There is some convergence on NMDA receptor antagonism as a likely, but to date unproven, common mechanism. The surprising number of other mechanisms, and the several novel biochemical aetiologies of depression proposed, suggests exciting new drug-discovery targets.
大量临床数据现已证实,与目前抗抑郁药物起效延迟(通常为数周)不同,氯胺酮能产生显著的快速起效的抗抑郁作用——数小时或数天。这一惊人且具有革命性的发现可能会通过降低当前药物起效延迟所带来的高自杀风险,推动开发挽救生命的抑郁症药物治疗方法。由于氯胺酮存在严重的自我限制缺陷,限制了其在此用途上的广泛应用,因此需要一种更安全的替代药物。我们的目的是回顾氯胺酮快速起效抗抑郁作用的推测机制,以深入了解抑郁症的生理基础,从而为抗抑郁药物研发找到新的靶点。
对已发表的文献(如PubMed)和网络资源进行检索,以确定与氯胺酮快速起效抗抑郁作用相关的信息,特别是该作用可能的机制。关键检索词包括“氯胺酮”“抗抑郁药”“作用机制”“抑郁症”和“快速起效”,可单独或组合使用。收集的信息将包括氯胺酮不太为人所知以及为人熟知的基本药理特性,并识别和评估关于氯胺酮抗抑郁作用机制的几种假说。
氯胺酮快速起效抗抑郁作用的机制解释是与其众所周知的对谷氨酸受体NMDA(N-甲基-D-天冬氨酸)亚型的拮抗作用有关,还是与其他因素有关,目前尚未完全阐明。来自药理学、药物化学、动物模型和药物研发来源的证据揭示了多种推测机制。
氯胺酮快速起效抗抑郁作用的惊人发现改变了对抑郁症的理解和治疗方式。NMDA受体拮抗作用作为一种可能但尚未得到证实的共同机制,已出现了一些共识。其他机制数量惊人,以及提出的几种抑郁症新的生化病因,提示了令人兴奋的新药研发靶点。