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P2X7 受体作为重度抑郁症的一个潜在靶点。

P2X7 Receptor as a Potential Target for Major Depressive Disorder.

机构信息

Department of Histology and Embryology, Institute of Clinical Anatomy & Reproductive Medicine, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang Medical College, University of South China, 421001, Hunan, China.

出版信息

Curr Drug Targets. 2021;22(10):1108-1120. doi: 10.2174/1389450122666210120141908.

Abstract

Major depressive disorder (MDD) is a common mental disorder. Although the genetic, biochemical, and psychological factors have been related to the development of MDD, it is generally believed that a series of pathological changes in the brain caused by chronic stress is the main cause of MDD. However, the specific mechanisms underlying chronic stress-induced MDD are largely undermined. Recent investigations have found that increased pro-inflammatory cytokines and changes in the inflammatory pathway in the microglia cells in the brain are the potential pathophysiological mechanism of MDD. P2X7 receptor (P2X7R) and its mediated signaling pathway play a key role in microglia activation. The present review aimed to present and discuss the accumulating data on the role of P2X7R in MDD. Firstly, we summarized the research progress in the correlation between P2X7R and MDD. Subsequently, we presented the P2X7R mediated microglia activation in MDD and the role of P2X7R in increased blood-brain barrier (BBB) permeability caused by chronic stress. Lastly, we also discussed the potential mechanism underlying-P2X7R expression changes after chronic stress. In conclusion, P2X7R is a key molecule regulating the activation of microglia. Chronic stress activates microglia in the hippocampus by secreting interleukin- 1β (IL-1β) and other inflammatory cytokines, and increasing the BBB permeability, thus promoting the occurrence and development of MDD, which indicated that P2X7R might be a promising therapeutic target for MDD.

摘要

重度抑郁症(MDD)是一种常见的精神障碍。尽管遗传、生化和心理因素与 MDD 的发展有关,但人们普遍认为,慢性应激引起的一系列大脑病理性变化是 MDD 的主要原因。然而,慢性应激诱导的 MDD 的具体机制在很大程度上仍未得到阐明。最近的研究发现,大脑中小胶质细胞中促炎细胞因子的增加和炎症途径的改变是 MDD 的潜在病理生理机制。P2X7 受体(P2X7R)及其介导的信号通路在小胶质细胞激活中起关键作用。本综述旨在介绍和讨论 P2X7R 在 MDD 中的作用的积累数据。首先,我们总结了 P2X7R 与 MDD 之间的相关性的研究进展。随后,我们介绍了 P2X7R 介导的小胶质细胞在 MDD 中的激活以及 P2X7R 在慢性应激引起的血脑屏障(BBB)通透性增加中的作用。最后,我们还讨论了慢性应激后 P2X7R 表达变化的潜在机制。总之,P2X7R 是调节小胶质细胞激活的关键分子。慢性应激通过分泌白细胞介素-1β(IL-1β)和其他炎症细胞因子激活海马小胶质细胞,并增加 BBB 通透性,从而促进 MDD 的发生和发展,这表明 P2X7R 可能是治疗 MDD 的有希望的靶点。

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