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神经炎症的动物模型及潜在治疗方法

Animal Models for Neuroinflammation and Potential Treatment Methods.

作者信息

Tamura Yasuhisa, Yamato Masanori, Kataoka Yosky

机构信息

Laboratory for Cellular Function Imaging, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.

Multi-Modal Microstructure Analysis Unit, RIKEN-JEOL Collaboration Center, RIKEN, Kobe, Japan.

出版信息

Front Neurol. 2022 Jun 27;13:890217. doi: 10.3389/fneur.2022.890217. eCollection 2022.

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating chronic disease of unknown etiology and without effective treatment options. The onset of ME/CFS is often associated with neuroinflammation following bacterial or viral infection. A positron emission tomography imaging study revealed that the degree of neuroinflammation was correlated with the severity of several symptoms in patients with ME/CFS. In animal studies, lipopolysaccharide- and polyinosinic-polycytidylic acid-induced models are thought to mimic the pathological features of ME/CFS and provoke neuroinflammation, characterized by increased levels of proinflammatory cytokines and activation of microglia. In this review, we described the anti-inflammatory effects of three compounds on neuroinflammatory responses utilizing animal models. The findings of the included studies suggest that anti-inflammatory substances may be used as effective therapies to ameliorate disease symptoms in patients with ME/CFS.

摘要

肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)是一种病因不明且尚无有效治疗方案的使人衰弱的慢性疾病。ME/CFS的发病通常与细菌或病毒感染后的神经炎症有关。一项正电子发射断层扫描成像研究表明,神经炎症的程度与ME/CFS患者的几种症状的严重程度相关。在动物研究中,脂多糖和聚肌苷酸-聚胞苷酸诱导的模型被认为可模拟ME/CFS的病理特征并引发神经炎症,其特征是促炎细胞因子水平升高和小胶质细胞活化。在本综述中,我们利用动物模型描述了三种化合物对神经炎症反应的抗炎作用。纳入研究的结果表明,抗炎物质可用作改善ME/CFS患者疾病症状的有效疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/9271866/e769a77a442f/fneur-13-890217-g0001.jpg

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