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胆汁酸和去氧熊胆酸在非酒精性脂肪性肝病中的治疗机制

Therapeutic Mechanisms of Bile Acids and Nor-Ursodeoxycholic Acid in Non-Alcoholic Fatty Liver Disease.

作者信息

Steinacher Daniel, Claudel Thierry, Trauner Michael

机构信息

Hans Popper Laboratory of Molecular Hepatology, Division of Gastroenterology and Hepatology, Internal Medicine III, Medical University of Vienna, Vienna, Austria.

出版信息

Dig Dis. 2017;35(3):282-287. doi: 10.1159/000454853. Epub 2017 Mar 1.

Abstract

Non-alcoholic fatty liver disease is one of the most rapidly rising clinical problems in the 21st century. So far no effective drug treatment has been established to cure this disease. Bile acids (BAs) have a variety of signaling properties, which can be used therapeutically for modulating hepatic metabolism and inflammation. A side-chain shorted derivative of ursodeoxycholic acid (UDCA) is 24 nor-ursodeoxycholic acid (NorUDCA) and it represents a new class of drugs for treatment of liver diseases. NorUDCA has unique biochemical and therapeutic properties, since it is relatively resistant to conjugation with glycine or taurine compared to UDCA. NorUDCA undergoes cholehepatic shunting, resulting in ductular targeting, bicarbonate-rich hypercholeresis, and cholangiocyte protection. Furthermore, it showed anti-fibrotic, anti-inflammatory, and anti-lipotoxic properties in several animal models. As such, NorUDCA is a promising new approach in the treatment of cholestatic and metabolic liver diseases. This review is a summary of current BA-based therapeutic approaches in the treatment of the fatty liver disease.

摘要

非酒精性脂肪性肝病是21世纪临床发病率上升最快的疾病之一。迄今为止,尚未确立有效的药物治疗方法来治愈该疾病。胆汁酸(BAs)具有多种信号传导特性,可用于调节肝脏代谢和炎症的治疗。熊去氧胆酸(UDCA)的一种侧链缩短衍生物是24-去甲熊去氧胆酸(NorUDCA),它代表了一类用于治疗肝病的新型药物。NorUDCA具有独特的生化和治疗特性,因为与UDCA相比,它相对不易与甘氨酸或牛磺酸结合。NorUDCA进行胆肝分流,导致小胆管靶向、富含碳酸氢盐的胆汁分泌过多和胆管细胞保护。此外,它在几种动物模型中显示出抗纤维化、抗炎和抗脂毒性特性。因此,NorUDCA是治疗胆汁淤积性和代谢性肝病的一种有前景的新方法。本综述总结了目前基于胆汁酸的治疗方法在治疗脂肪性肝病方面的应用。

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