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氯胺酮通过下调慢性束缚应激诱导的小鼠炎性细胞因子来减轻抑郁样行为。

Ketamine Alleviates Depressive-Like Behaviors via Down-Regulating Inflammatory Cytokines Induced by Chronic Restraint Stress in Mice.

作者信息

Tan Sijie, Wang Yan, Chen Ke, Long Zhifeng, Zou Ju

机构信息

Department of Histology and Embryology, School of Medicine, University of South China.

Department of Ultrasound Diagnosis, Affiliated Nanhua Hospital, University of South China.

出版信息

Biol Pharm Bull. 2017;40(8):1260-1267. doi: 10.1248/bpb.b17-00131.

Abstract

The purpose of the present study was to investigate whether ketamine's rapid antidepressant effects were associated with its anti-inflammatory actions and to explore the underlying molecular mechanism. Depressive-like behaviors was induced in mice using chronic restraint stress (CRS) method. Anti-depressive effects of ketamine were evaluated by forced swimming tests (FST) and sucrose preference test (SPT). Subsequently, brain tissue was harvested to investigate inflammatory response in the hippocampus via investigating reactive microglia numbers, serum cytokines levels and the toll-like receptor type 4 (TLR4)/p38 mitogen-activated protein kinase (MAPK) pathway. CRS exposure caused depressive-like behaviors in mice, which was associated with increased pre-inflammatory cytokines (interleukin (IL)-1β, tumor necrosis factor (TNF)-α and IL-6) levels, reactive microglia numbers and up-regulated regulatory molecules such as TLR4/p38 and P2X7 receptor in hippocampus. Such neurobehavioral and biochemical abnormalities were normalized by ketamine treatment. CRS-induced depression-like behaviours are associated with activation of hippocampal inflammatory response, whereas down-regulation of pro-inflammatory cytokines may contribute to ketamine's antidepressant effects in mice.

摘要

本研究的目的是调查氯胺酮的快速抗抑郁作用是否与其抗炎作用相关,并探索其潜在的分子机制。采用慢性束缚应激(CRS)方法诱导小鼠出现抑郁样行为。通过强迫游泳试验(FST)和蔗糖偏好试验(SPT)评估氯胺酮的抗抑郁作用。随后,采集脑组织,通过研究反应性小胶质细胞数量、血清细胞因子水平以及Toll样受体4(TLR4)/p38丝裂原活化蛋白激酶(MAPK)通路来研究海马体中的炎症反应。CRS暴露导致小鼠出现抑郁样行为,这与海马体中炎症前细胞因子(白细胞介素(IL)-1β、肿瘤坏死因子(TNF)-α和IL-6)水平升高、反应性小胶质细胞数量增加以及TLR4/p38和P2X7受体等调节分子上调有关。氯胺酮治疗可使这些神经行为和生化异常恢复正常。CRS诱导的抑郁样行为与海马体炎症反应的激活有关,而促炎细胞因子的下调可能有助于氯胺酮对小鼠的抗抑郁作用。

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