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利伐沙班改善多发性硬化症动物模型的病程。

Rivaroxaban ameliorates disease course in an animal model of multiple sclerosis.

作者信息

Merker Monika, Eichler Susann, Herrmann Alexander M, Wiendl Heinz, Kleinschnitz Christoph, Göbel Kerstin, Meuth Sven G

机构信息

Department of Neurology, University of Münster, Münster, Germany.

Department of Neurology, University Hospital Essen, 45147 Essen, Germany.

出版信息

J Neuroimmunol. 2017 Dec 15;313:125-128. doi: 10.1016/j.jneuroim.2017.08.013. Epub 2017 Sep 21.

Abstract

Recent studies have implicated an important role for coagulation factors in neuroinflammatory disorders like multiple sclerosis (MS). Here, we investigate the role of factor X (FX) in neuroinflammation by using rivaroxaban the selective inhibitor of activated FX (FXa) in experimental autoimmune encephalomyelitis (EAE, an animal model of MS). Rivaroxaban-treated rats were less susceptible to EAE compared to the untreated control group. This finding was accompanied by reduced T-cell infiltration and microglia activation. Our study identifies FX as a possible target in neuroinflammatory diseases. As FXa inhibitors are approved for other disorders, FXa blockade could serve as a fast available medication.

摘要

最近的研究表明,凝血因子在多发性硬化症(MS)等神经炎症性疾病中起着重要作用。在此,我们通过使用利伐沙班(活化因子X(FXa)的选择性抑制剂),在实验性自身免疫性脑脊髓炎(EAE,MS的动物模型)中研究因子X(FX)在神经炎症中的作用。与未治疗的对照组相比,接受利伐沙班治疗的大鼠对EAE的易感性较低。这一发现伴随着T细胞浸润和小胶质细胞活化的减少。我们的研究确定FX是神经炎症性疾病的一个可能靶点。由于FXa抑制剂已被批准用于其他疾病,FXa阻断可作为一种快速可用的药物。

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