抗抑郁药
神经科学
致电离效应
氯胺酮
谷氨酸的
突触可塑性
情绪障碍
NMDA受体
心理学
突触
医学
谷氨酸受体
精神科
海马体
受体
焦虑
内科学
作者
John H. Krystal,Ege T. Kavalali,Lisa M. Monteggia
标识
DOI:10.1038/s41386-023-01629-w
摘要
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.
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