奥贝胆酸-药理与临床研究进展

Caezaan Keshvani, J. Kopel, H. Goyal
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引用次数: 1

摘要

Obeticholic acid (OCA)或6- α -乙基鹅去氧胆酸是一种半合成的改性胆汁酸衍生物,作为激动剂作用于farnesoid X受体(FXR),其效力高于胆汁酸。FXR是一种核受体,在肝脏和小肠中高度表达,调节胆汁酸、胆固醇、葡萄糖代谢、炎症和细胞凋亡。FXR组胆汁酸受体目前正在研究其在治疗原发性胆汁性肝硬化(PBC)、非酒精性脂肪性肝炎(NASH)和原发性硬化性胆管炎(PSC)中的潜在作用。最近的临床研究表明,OCA可能与脂质调节药物协同作用,进一步改善原发性硬化性胆管炎的长期预后。具体而言,OCA可以改善具有不同组织学、代谢和生化问题的NASH患者的临床结果,并改善PBC、PSC或肝脏疾病患者的发病率和死亡率。这种改善体现在组织学检查的改善和移植需求的减少上。在这篇综述中,我们研究了OCA治疗PBC难治性脂肪性肝炎(NASH)的药理学。此外,我们探讨了OCA在PBC、PSC、NASH和NAFLD中的未来发展方向和应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obeticholic Acid—A Pharmacological and Clinical Review
Obeticholic acid (OCA) or 6-alpha-ethyl-chenodeoxycholic acid is a semisynthetic modified bile acid derivative that acts on the farnesoid X receptor (FXR) as an agonist with a higher potency than bile acid. The FXR is a nuclear receptor highly expressed in the liver and small intestine and regulates bile acid, cholesterol, glucose metabolism, inflammation, and apoptosis. The FXR group of bile acid receptors is currently under investigation for their potential role in the treatment of primary biliary cirrhosis (PBC), non-alcoholic steatohepatitis (NASH), and primary sclerosing cholangitis (PSC). Recent clinical studies suggest OCA may work synergistically with lipid modifying medications to further improve long-term outcomes with primary sclerosing cholangitis. Specifically, OCA can improve clinical outcomes in NASH patients with their different histological, metabolic, and biochemical issues as well as improve morbidity and mortality in patients suffering from PBC, PSC, or liver disease. This improvement is noted in both improved histological examination and reduced need for transplantation. In this review, we examine the pharmacology of OCA towards the treatment of PBC refractory and steatohepatitis (NASH). In addition, we examine future directions and applications of OCA for PBC, PSC, NASH, and NAFLD.
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