胸腺酚通过抑制小胶质细胞介导的神经炎症改善缺血性脑损伤

IF 3.5 3区 医学 Q2 NEUROSCIENCES
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引用次数: 0

摘要

背景:小胶质细胞介导的炎症是缺血性中风恶化的关键因素。因此,减轻小胶质细胞的过度活化是治疗缺血性损伤的一种潜在策略。百里酚是一种从植物精油中提取的单酚,具有多种有益的生物活性,包括抗炎和抗氧化特性,在各种疾病模型中都显示出保护作用。然而,它对缺血性中风和小胶质细胞炎症的具体作用仍有待探索:方法:建立啮齿动物瞬时大脑中动脉闭塞(tMCAO)模型来模拟缺血性中风。TTC染色、改良神经功能评分(mNSS)和行为测试用于评估神经损伤的严重程度。然后用免疫荧光染色和细胞骨架分析来确定小胶质细胞的激活情况。利用脂多糖(LPS)诱导体外原代小胶质细胞的炎症反应。采用实时定量聚合酶链反应(qRT-PCR)、Western 印迹和酶联免疫吸附试验(ELISA)检测炎症细胞因子的表达。结果表明,百里酚具有抗炎作用:结果:本研究发现,胸腺酚治疗可通过减轻微胶质细胞活化和促炎反应(IL-1β、IL-6和TNF-α)改善卒中后神经功能损伤并减少梗死体积。在机制上,胸腺酚可抑制磷脂酰肌醇-3-激酶(PI3K)、丝氨酸/苏氨酸激酶(Akt)和哺乳动物雷帕霉素靶标(mTOR)的磷酸化,从而抑制核因子-κB(NF-κB)的激活:我们的研究表明,胸腺酚可以通过靶向PI3K/Akt/mTOR/NF-κB信号通路来减轻小胶质细胞炎症,最终缓解缺血性脑损伤。这些研究结果表明,胸腺酚是一种很有前景的缺血性脑卒中神经保护剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thymol improves ischemic brain injury by inhibiting microglia-mediated neuroinflammation

Background

Microglia-mediated inflammation is a critical factor in the progression of ischemic stroke. Consequently, mitigating excessive microglial activation represents a potential therapeutic strategy for ischemic injury. Thymol, a monophenol derived from plant essential oils, exhibits diverse beneficial biological activities, including anti-inflammatory and antioxidant properties, with demonstrated protective effects in various disease models. However, its specific effects on ischemic stroke and microglial inflammation remain unexplored.

Methods

Rodent transient middle cerebral artery occlusion (tMCAO) model was established to simulate ischemic stroke. TTC staining, modified neurological function score (mNSS), and behavioral tests were used to assess the severity of neurological damage. Then immunofluorescence staining and cytoskeleton analysis were used to determine activation of microglia. Lipopolysaccharide (LPS) was utilized to induce the inflammatory response of primary microglia in vitro. Quantitative real-time polymerase chain reaction (qRT-PCR), western blot, and enzyme-linked immunosorbent assay (ELISA) were performed to exam the expression of inflammatory cytokines. And western blot was used to investigate the mechanism of the anti-inflammatory effect of thymol.

Results

In this study, we found that thymol treatment could ameliorate post-stroke neurological impairment and reduce infarct volume by mitigating microglial activation and pro-inflammatory response (IL-1β, IL-6, and TNF-α). Mechanically, thymol could inhibit the phosphorylation of phosphatidylinositol-3-kinase (PI3K), sink serine/threonine kinase (Akt), and mammalian target of rapamycin (mTOR), thereby suppressing the activation of nuclear factor-κB (NF-κB).

Conclusions

Our study demonstrated that thymol could reduce the microglial inflammation by targeting PI3K/Akt/mTOR/NF-κB signaling pathway, ultimately alleviating ischemic brain injury. These findings suggest that thymol is a promising candidate as a neuroprotective agent against ischemic stroke.

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来源期刊
Brain Research Bulletin
Brain Research Bulletin 医学-神经科学
CiteScore
6.90
自引率
2.60%
发文量
253
审稿时长
67 days
期刊介绍: The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.
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