解码抑郁症:从神经胶质和氯胺酮调节外侧缰神经突放电的见解。

Yihui Cui, Yan Yang, Yiyan Dong, Hailan Hu
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引用次数: 13

摘要

氯胺酮的快速抗抑郁作用可以说是过去半个世纪精神健康领域最重要的进步之一。然而,其作用机制尚不清楚。在这里,我们描述了我们最新的发现,氯胺酮如何阻断大脑中n -甲基-d -天冬氨酸受体(NMDAR)依赖的“抗奖励”中心,侧缰核(LHb)的爆发,以调节其抗抑郁作用。我们还讨论了神经胶质-神经元界面的一种新的结构-功能机制,以解释抑郁症期间LHb破裂的增强。这些结果为重性抑郁症的治疗干预提供了新的分子靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decoding Depression: Insights from Glial and Ketamine Regulation of Neuronal Burst Firing in Lateral Habenula.

The rapid antidepressant effect of ketamine is arguably one of the most significant advances in the mental health field in the last half century. However, its mechanism of action has remained elusive. Here, we describe our latest discovery on how ketamine blocks N-methyl-D-aspartate receptor (NMDAR)-dependent burst firing of an "antireward" center in the brain, the lateral habenula (LHb), to mediate its antidepressant effects. We also discuss a novel structure-function mechanism at the glia-neuron interface to account for the enhanced LHb bursting during depression. These results reveal new molecular targets for the therapeutic intervention of major depression.

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