Ursodiol: a cholesterol gallstone solubilizing agent.

C L Rosenbaum, R J Cluxton
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引用次数: 4

Abstract

Ursodiol, a naturally occurring bile acid, has gained Food and Drug Administration approval for the dissolution of cholesterol gallstones. Ursodiol inhibits hepatic cholesterol synthesis and secretion. Lithocholic acid, a potentially hepatotoxic metabolite of ursodiol and chenodiol, may accumulate to a lesser extent with ursodiol than with chenodiol. Enterohepatic recirculation of ursodiol and its metabolites occurs and is essential to the dissolution of cholesterol gallstones. Complete dissolution has been achieved in 17 percent of patients with noncalcified, radiolucent, floating, cholesterol gallstones. Recurrence of cholesterol gallstones may occur in over one-half of initial responders. Diarrhea reported in up to 50 percent of the patients on chenodiol has been reported in only 4 percent of patients treated with ursodiol. Increased mean aspartate aminotransferase levels to more than twice the pretreatment level seen with chenodiol therapy have not been reported with ursodiol. Reportedly fewer adverse reactions may give ursodiol a major advantage over chenodiol in hospital formulary considerations.

熊二醇:一种胆固醇胆结石增溶剂。
熊二醇是一种天然产生的胆汁酸,已获得食品和药物管理局批准用于溶解胆固醇胆结石。熊二醇抑制肝脏胆固醇的合成和分泌。石胆酸是熊二醇和鹅二醇的潜在肝毒性代谢物,与鹅二醇相比,石胆酸在熊二醇中的积累程度较小。熊二醇及其代谢物发生肠肝再循环,对胆固醇胆结石的溶解至关重要。17%的非钙化、透光、漂浮、胆固醇型胆结石患者实现了完全溶解。超过一半的初始应答者可能会出现胆固醇结石的复发。据报道,在接受鹅二醇治疗的患者中,高达50%的患者出现腹泻,而接受熊二醇治疗的患者中只有4%出现腹泻。升高的平均天冬氨酸转氨酶水平比鹅二醇治疗前水平的两倍还未见熊二醇治疗的报道。据报道,在医院处方考虑中,较少的不良反应可能使熊二醇比鹅二醇具有主要优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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