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背缝核 5-羟色胺能神经元中 p11 的减少介导了抑郁样行为。

Reduction of p11 in dorsal raphe nucleus serotonergic neurons mediates depression-like behaviors.

机构信息

Department of Acupuncture and Moxibustion, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 200071, China.

Department of Integrative Medicine and Neurobiology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai, 200032, China.

出版信息

Transl Psychiatry. 2023 Nov 22;13(1):359. doi: 10.1038/s41398-023-02664-3.

Abstract

The pathology of depression is related to the imbalance of various neurotransmitters. The dorsal raphe nucleus (DRN), the main brain region producing 5-HT, is crucially involved in the pathophysiology of depression. It contains several neuron types, in which GABAergic neurons are activated by stimuli associated with negative experiences and 5-HT neurons are activated by reward signals. However, little is known about its underlying molecular mechanisms. Here, we found that p11, a multifunctional protein associated with depression, was down-regulated by chronic social defeat stress in 5-HT neurons. Knockdown of p11 in DRN induced depression-like behaviors, while its overexpression in 5-HT neurons alleviated depression-like behavior caused by chronic social defeat stress. Further, p11 regulates membrane trafficking of glutamate receptors in 5-HT neurons, suggesting a possible molecular mechanism underlying the participation of p11 in the pathological process of depression. This may facilitate the understanding of the molecular and cellular basis of depression.

摘要

抑郁症的病理学与各种神经递质的失衡有关。中缝背核(DRN)是产生 5-HT 的主要脑区,它在抑郁症的病理生理学中起着至关重要的作用。它包含几种神经元类型,其中 GABA 能神经元被与负面经历相关的刺激激活,而 5-HT 神经元被奖励信号激活。然而,其潜在的分子机制知之甚少。在这里,我们发现与抑郁症相关的多功能蛋白 p11 可被慢性社交挫败应激下调。DRN 中 p11 的敲低会诱导出类似抑郁的行为,而其在 5-HT 神经元中的过表达则可以减轻慢性社交挫败应激引起的类似抑郁的行为。此外,p11 调节 5-HT 神经元中谷氨酸受体的膜转运,提示 p11 参与抑郁症病理过程的可能分子机制。这可能有助于理解抑郁症的分子和细胞基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bcf/10665321/d6e376165a8d/41398_2023_2664_Fig1_HTML.jpg

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