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Anti-inflammatory activity of berberine in non-alcoholic fatty liver disease via the Angptl2 pathway

机译:通过Angptl2途径通过植物脂肪肝病的Berberine抗炎活性

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Nonalcoholic fatty liver disease (NAFLD) has become the most common liver disease worldwide. Recent studies have shown that the Angptl2 pathway mediated hepatic inflammatory response plays an important role in the progression of nonalcoholic fatty liver disease. Our study investigated the possible molecular mechanisms of berberine (BBR) in the treatment of the liver inflammatory response in the livers of rats with high-fat diet-induced NAFLD via the Angptl2 pathway. At the end of 12?weeks, compared with the control group rats, the high-fat- diet group rats showed obvious pathological and biochemical changes. The levels of pro-infalmmatory cytokines (CCL2, TNF-α) were increased, the infiltration of inflammatory cells (CCR2) was elevated, and the hepatic mRNA and protein levels of Angptl2, NF-κB and Foxo1 were increased to different degrees. Nevertheless, following treatment with BBR, liver tissue pathology, biochemical data, and Angptl2 pathway-related genes expression were significantly ameliorated. Our findings demonstrate that BBR might attenuate the liver inflammatory response in the livers of rats with high-fat diet-induced NAFLD through the regulation of the Angptl2 pathway.
机译:非酒精性脂肪肝病(NAFLD)已成为全球最常见的肝病。最近的研究表明,Angptl2途径介导的肝炎症反应在非酒精性脂肪肝疾病的进展中起重要作用。我们的研究调查了Berberine(BBR)在通过Angptl2途径通过高脂饮食诱导的NAFLD治疗肝脏炎症反应治疗肝脏炎症反应的可能分子机制。在12岁以下?几周后,与对照组大鼠相比,高脂饮食群大鼠表现出明显的病理和生化变化。增加了促血管体细胞因子(CCL2,TNF-α)的水平,炎症细胞(CCR2)的浸润升高,肝脏mRNA和Angptl2,NF-κB和FOXO1的肝蛋白水平增加到不同程度。然而,随后用BBR,肝组织病理学,生物化学数据和Angptl2途径相关基因表达进行了显着改善。我们的研究结果表明,BBR通过调节Angptl2途径,BBR可能会衰减具有高脂饮食诱导的NAFLD的大鼠肝脏炎症反应。

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