Literature DB >> 7630925

Ursodeoxycholic acid therapy of chronic cholestatic conditions in adults and children.

R Poupon1, R E Poupon.   

Abstract

Cholestasis can be defined as the manifestation of defective bile acid transport from the liver to the intestine. Most chronic cholestatic conditions can progress towards cirrhosis. At this stage, liver transplantation is the treatment of choice. Most of the drugs so far evaluated show some degree of efficacy but have major side effects. Given that ursodeoxycholic acid (UDCA) has no apparent toxicity in humans, it was postulated that long-term treatment with this drug might displace endogenous bile acids and thus reverse their suspected toxicity. We demonstrated that long-term UDCA therapy slows the progression of primary biliary cirrhosis and reduces the need for liver transplantation. In this review, we give the rationale for the use of UDCA in cholestasis and discuss its possible mechanisms of action. We also give an overview of current data on UDCA therapy of chronic cholestatic disorders in adults and children.

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Year:  1995        PMID: 7630925     DOI: 10.1016/0163-7258(94)00073-c

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


  12 in total

Review 1.  Ursodeoxycholic acid treatment of vanishing bile duct syndromes.

Authors:  Thomas Pusl; Ulrich Beuers
Journal:  World J Gastroenterol       Date:  2006-06-14       Impact factor: 5.742

Review 2.  Animal models to study bile acid metabolism.

Authors:  Jianing Li; Paul A Dawson
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2018-05-18       Impact factor: 5.187

3.  Phosphoinositide 3-kinase-dependent Ras activation by tauroursodesoxycholate in rat liver.

Authors:  A K Kurz; C Block; D Graf; S V Dahl; F Schliess; D Häussinger
Journal:  Biochem J       Date:  2000-08-15       Impact factor: 3.857

4.  Pretreatment with ursodeoxycholic acid (UDCA) as a novel pharmacological intervention in hepatobiliary scintigraphy.

Authors:  Hwan Jeong Jeong; Chang Guhn Kim
Journal:  Yonsei Med J       Date:  2005-06-30       Impact factor: 2.759

5.  A clinical-morphological study on cholestatic presentation of nonalcoholic fatty liver disease.

Authors:  P Sorrentino; G Tarantino; A Perrella; P Micheli; O Perrella; P Conca
Journal:  Dig Dis Sci       Date:  2005-06       Impact factor: 3.199

6.  Effect of deoxycholic acid and ursodeoxycholic acid on lipid peroxidation in cultured macrophages.

Authors:  P Ljubuncic; B Fuhrman; J Oiknine; M Aviram; A Bomzon
Journal:  Gut       Date:  1996-09       Impact factor: 23.059

Review 7.  [Treatment of cholestatic hepatic diseases: more than the substitution of fat soluble vitamins?].

Authors:  J Pausch; M Gatzen
Journal:  Internist (Berl)       Date:  2006-12       Impact factor: 0.743

8.  Simple determination of deoxycholic and ursodeoxycholic acids by phenolphthalein-beta-cyclodextrin inclusion complex.

Authors:  Pabyton G Cadena; Eric C Oliveira; Alberto N Araújo; Maria C B S M Montenegro; Maria C B Pimentel; José L Lima Filho; Valdinete L Silva
Journal:  Lipids       Date:  2009-10-11       Impact factor: 1.880

9.  Contribution of the 7β-hydroxysteroid dehydrogenase from Ruminococcus gnavus N53 to ursodeoxycholic acid formation in the human colon.

Authors:  Ja-Young Lee; Hisashi Arai; Yusuke Nakamura; Satoru Fukiya; Masaru Wada; Atsushi Yokota
Journal:  J Lipid Res       Date:  2013-06-01       Impact factor: 5.922

10.  Ursodeoxycholic acid inhibits liver X receptor α-mediated hepatic lipogenesis via induction of the nuclear corepressor SMILE.

Authors:  Ji-Min Lee; Gil-Tae Gang; Don-Kyu Kim; Yong Deuk Kim; Seung-Hoi Koo; Chul-Ho Lee; Hueng-Sik Choi
Journal:  J Biol Chem       Date:  2013-11-21       Impact factor: 5.157

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