新型速效抗抑郁药:分子和细胞信号机制。

Q4 Neuroscience
Neuronal signaling Pub Date : 2017-12-01 Epub Date: 2017-09-05 DOI:10.1042/NS20170010
Alexandra M Thomas, Ronald S Duman
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引用次数: 12

摘要

抑郁症是一种慢性、使人衰弱的常见病。目前可用的药物治疗是有帮助的,但有几个主要的缺点,包括相当低的反应率或没有反应和治疗时间较长。为了寻求更好的治疗选择,最近的研究集中在速效抗抑郁药上,包括n -甲基- d-天冬氨酸(NMDA)受体(NMDAR)拮抗剂氯胺酮,它以不同于典型抗抑郁药的机制影响一系列信号通路。由于氯胺酮和类似的药物有望显著改善抑郁症患者的治疗选择,人们对开发新方法来了解这些化合物如何影响大脑产生了相当大的兴趣。在这里,我们回顾了目前对速效抗抑郁药如何起作用的理解,包括它们对神经元信号通路和神经回路的影响,以及用于解决这些问题的研究技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel rapid-acting antidepressants: molecular and cellular signaling mechanisms.

Novel rapid-acting antidepressants: molecular and cellular signaling mechanisms.

Novel rapid-acting antidepressants: molecular and cellular signaling mechanisms.

Depression is a chronic, debilitating, and common illness. Currently available pharmacotherapies can be helpful but have several major drawbacks, including substantial rates of low or no response and a long therapeutic time lag. In pursuit of better treatment options, recent research has focussed on rapid-acting antidepressants, including the N-methyl-D-aspartate (NMDA) receptor (NMDAR) antagonist ketamine, which affects a range of signaling pathways in ways that are distinct from the mechanisms of typical antidepressants. Because ketamine and similar drugs hold the promise of dramatically improving treatment options for depressed patients, there has been considerable interest in developing new ways to understand how these compounds affect the brain. Here, we review the current understanding of how rapid-acting antidepressants function, including their effects on neuronal signaling pathways and neural circuits, and the research techniques being used to address these questions.

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来源期刊
CiteScore
4.60
自引率
0.00%
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审稿时长
14 weeks
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