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SREBP-1c overexpression induces triglycerides accumulation through increasing lipid synthesis and decreasing lipid oxidation and VLDL assembly in bovine hepatocytes.固醇调节元件结合蛋白1c(SREBP-1c)的过表达通过增加脂质合成、减少脂质氧化以及极低密度脂蛋白(VLDL)组装,诱导牛肝细胞内甘油三酯蓄积。
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Nonalcoholic fatty liver disease is associated with aortic valve sclerosis in patients with type 2 diabetes mellitus.非酒精性脂肪性肝病与2型糖尿病患者的主动脉瓣硬化有关。
PLoS One. 2014 Feb 5;9(2):e88371. doi: 10.1371/journal.pone.0088371. eCollection 2014.
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[Effects of farnesoid X receptor agonist on adiponectin and its receptors].法尼酯X受体激动剂对脂联素及其受体的影响
Nan Fang Yi Ke Da Xue Xue Bao. 2014 Jan;34(1):109-12.
4
Increased risk of colorectal malignant neoplasm in patients with nonalcoholic fatty liver disease: a large study.非酒精性脂肪性肝病患者患结直肠恶性肿瘤的风险增加:一项大型研究。
Mol Biol Rep. 2014 May;41(5):2989-97. doi: 10.1007/s11033-014-3157-y. Epub 2014 Jan 22.
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Nonalcoholic steatohepatitis is the most rapidly growing indication for liver transplantation in patients with hepatocellular carcinoma in the U.S.非酒精性脂肪性肝炎是美国肝细胞癌患者进行肝移植的增长最快的指征。
Hepatology. 2014 Jun;59(6):2188-95. doi: 10.1002/hep.26986. Epub 2014 Apr 25.
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Hepatic steatosis exacerbated by endoplasmic reticulum stress-mediated downregulation of FXR in aging mice.衰老小鼠内质网应激介导的 FXR 下调加剧肝脂肪变性。
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7
Systematic review with meta-analysis: non-invasive assessment of non-alcoholic fatty liver disease--the role of transient elastography and plasma cytokeratin-18 fragments.系统评价与荟萃分析:非酒精性脂肪性肝病的无创性评估——瞬时弹性成像和血浆细胞角蛋白 18 片段的作用。
Aliment Pharmacol Ther. 2014 Feb;39(3):254-69. doi: 10.1111/apt.12569. Epub 2013 Dec 5.
8
Activation of farnesoid X receptor induces RECK expression in mouse liver.法尼醇 X 受体的激活诱导小鼠肝脏中 REck 的表达。
Biochem Biophys Res Commun. 2014 Jan 3;443(1):211-6. doi: 10.1016/j.bbrc.2013.11.082. Epub 2013 Nov 28.
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Activation of farnesoid X receptor attenuates hepatic injury in a murine model of alcoholic liver disease.法尼醇 X 受体的激活可减轻酒精性肝病小鼠模型中的肝损伤。
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10
Association between nonalcoholic fatty liver disease and the incidence of cardiovascular and renal events.非酒精性脂肪性肝病与心血管及肾脏事件发生率之间的关联。
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法尼醇X受体在非酒精性脂肪性肝病中的最新研究进展

Recent insights into farnesoid X receptor in non-alcoholic fatty liver disease.

作者信息

Xu Jiao-Ya, Li Zhong-Ping, Zhang Li, Ji Guang

机构信息

Jiao-Ya Xu, Zhong-Ping Li, Li Zhang, Guang Ji, Institute of Digestive Diseases, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China.

出版信息

World J Gastroenterol. 2014 Oct 7;20(37):13493-500. doi: 10.3748/wjg.v20.i37.13493.

DOI:10.3748/wjg.v20.i37.13493
PMID:25309079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4188900/
Abstract

Non-alcoholic fatty liver disease (NAFLD) is the hepatic manifestation of metabolic syndrome and is one of the most prevalent liver disorders worldwide. NAFLD can gradually progress to liver inflammation, fibrosis, cirrhosis and even hepatocellular carcinoma. However, the pathogenesis of NAFLD is complex, and no efficient pharmaceutic treatments have yet been established for NAFLD. Accumulating data have shown that the farnesoid X receptor (FXR) plays important roles not only in bile acid metabolism, but also in lipid and carbohydrate homeostasis, inflammatory responses, among others. In this review, we aim to highlight the role of FXR in the pathogenesis and treatment of NAFLD.

摘要

非酒精性脂肪性肝病(NAFLD)是代谢综合征的肝脏表现,也是全球最常见的肝脏疾病之一。NAFLD可逐渐发展为肝脏炎症、纤维化、肝硬化甚至肝细胞癌。然而,NAFLD的发病机制复杂,目前尚未建立有效的药物治疗方法。越来越多的数据表明,法尼醇X受体(FXR)不仅在胆汁酸代谢中起重要作用,而且在脂质和碳水化合物稳态、炎症反应等方面也发挥重要作用。在本综述中,我们旨在强调FXR在NAFLD发病机制和治疗中的作用。