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免疫调节喹啉-3-甲酰胺帕奎莫德在新型肝纤维化小鼠模型中逆转已建立的纤维化。

The immunomodulatory quinoline-3-carboxamide paquinimod reverses established fibrosis in a novel mouse model for liver fibrosis.

机构信息

Department of Experimental Medical Science, Lund University, Lund, Sweden.

出版信息

PLoS One. 2018 Sep 5;13(9):e0203228. doi: 10.1371/journal.pone.0203228. eCollection 2018.

Abstract

Quinoline-3-carboxamides (Q substances) are small molecule compounds with anti-inflammatory properties. In this study, we used one of these substances, Paquinimod, to treat a novel model for chronic liver inflammation and liver fibrosis, the NOD-Inflammation Fibrosis (N-IF) mouse. We show that treatment of N-IF mice significantly reduced inflammation and resulted in the regression of fibrosis, even when the treatment was initiated after onset of disease. The reduced disease phenotype was associated with a systemic decrease in the number and reduced activation of disease-promoting transgenic natural killer T (NKT)-II cells and their type 2-cytokine expression profile. Paquinimod treatment also led to a reduction of CD115+ Ly6Chi monocytes and CD11b+ F4/80+ CD206+ macrophages.

摘要

喹啉-3-甲酰胺(Q 物质)是具有抗炎特性的小分子化合物。在这项研究中,我们使用了其中一种物质——派姆单抗(Paquinimod)来治疗一种新型的慢性肝脏炎症和肝纤维化模型,即 NOD-炎症纤维化(N-IF)小鼠。我们发现,派姆单抗治疗可显著减轻炎症,甚至在疾病开始后才开始治疗,也可使纤维化逆转。疾病表型的减轻与疾病促进型转基因自然杀伤 T(NKT)-II 细胞数量和激活的全身性减少以及它们的 2 型细胞因子表达谱有关。派姆单抗治疗还导致 CD115+Ly6Chi 单核细胞和 CD11b+F4/80+CD206+巨噬细胞的减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d6/6124744/5b0526bfd7d0/pone.0203228.g001.jpg

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