Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Department of Pharmacology and the Vanderbilt Brain Institute, Vanderbilt University, Nashville, TN, USA.
Neuropsychopharmacology. 2024 Jan;49(1):41-50. doi: 10.1038/s41386-023-01629-w. Epub 2023 Jul 24.
Ketamine is an open channel blocker of ionotropic glutamatergic N-Methyl-D-Aspartate (NMDA) receptors. The discovery of its rapid antidepressant effects in patients with depression and treatment-resistant depression fostered novel effective treatments for mood disorders. This discovery not only provided new insight into the neurobiology of mood disorders but also uncovered fundamental synaptic plasticity mechanisms that underlie its treatment. In this review, we discuss key clinical aspects of ketamine's effect as a rapidly acting antidepressant, synaptic and circuit mechanisms underlying its action, as well as how these novel perspectives in clinical practice and synapse biology form a road map for future studies aimed at more effective treatments for neuropsychiatric disorders.
氯胺酮是一种离子型谷氨酸能 N-甲基-D-天冬氨酸(NMDA)受体的非选择性通道阻断剂。氯胺酮在抑郁症和治疗抵抗性抑郁症患者中迅速抗抑郁作用的发现,为情绪障碍的治疗提供了新的有效治疗方法。这一发现不仅为情绪障碍的神经生物学提供了新的见解,而且揭示了其治疗作用的基本突触可塑性机制。在这篇综述中,我们讨论了氯胺酮作为一种快速作用的抗抑郁药的关键临床方面,其作用的突触和回路机制,以及这些在临床实践和突触生物学中的新观点如何为未来旨在更有效治疗神经精神疾病的研究制定路线图。