Literature DB >> 14585066

Hepatotoxicity of thiazolidinediones.

William L Isley1.   

Abstract

Thiazolidinediones are insulin sensitisers now widely used for the treatment of Type 2 diabetes mellitus. The initial marketed drug in this class, troglitazone, was removed from the market worldwide after approximately 3 years of use due to rare but severe hepatotoxicity, which sometimes resulted in liver failure leading to the need for liver transplantation, or even death. The unpredictability of such liver toxicity made the use of troglitazone highly problematic. Fortunately, the two newer drugs in this class, rosiglitazone and pioglitazone, have a much larger margin of safety for liver toxicity. Very rare reports of liver toxicity, usually milder and reversible, have been seen with these drugs. Therefore, whilst pharmacovigilance for hepatotoxicity is probably still warranted, the practitioner and patient can be fairly confident that these drugs are safe from a liver standpoint. Finally, recent work would suggest that these agents may prove useful to reduce hepatic fat in patients with non-alcoholic steatohepatitis, and may possibly protect against adverse metabolic consequences and the ultimate development of cirrhosis in patients with fatty livers.

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Year:  2003        PMID: 14585066     DOI: 10.1517/14740338.2.6.581

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  17 in total

1.  Fatal liver failure associated with pioglitazone.

Authors:  Ed Farley-Hills; R Sivasankar; M Martin
Journal:  BMJ       Date:  2004-08-21

2.  Enhanced insulin-hypoglycemic activity in rats consuming a specific glycoprotein extracted from maitake mushroom.

Authors:  Harry G Preuss; Bobby Echard; Debasis Bagchi; Nicholas V Perricone; Cun Zhuang
Journal:  Mol Cell Biochem       Date:  2007-08-01       Impact factor: 3.396

3.  Liver toxicity and pioglitazone: data are missing.

Authors:  Peshraw Amin
Journal:  BMJ       Date:  2004-10-16

4.  Role of physicochemical properties in the activation of peroxisome proliferator-activated receptor δ.

Authors:  Vinícius G Maltarollo; Paula Homem-de-Mello; Káthia M Honorio
Journal:  J Mol Model       Date:  2011-01-05       Impact factor: 1.810

5.  Assessment of drug-induced mitochondrial dysfunction via altered cellular respiration and acidification measured in a 96-well platform.

Authors:  Sashi Nadanaciva; Payal Rana; Gyda C Beeson; Denise Chen; David A Ferrick; Craig C Beeson; Yvonne Will
Journal:  J Bioenerg Biomembr       Date:  2012-06-12       Impact factor: 2.945

6.  Differences in hepatotoxicity and gene expression profiles by anti-diabetic PPAR gamma agonists on rat primary hepatocytes and human HepG2 cells.

Authors:  Lei Guo; Lu Zhang; Yongming Sun; Levan Muskhelishvili; Ernice Blann; Stacey Dial; Leming Shi; Gary Schroth; Yvonne P Dragan
Journal:  Mol Divers       Date:  2006-09-21       Impact factor: 2.943

7.  Microscale Collagen and Fibroblast Interactions Enhance Primary Human Hepatocyte Functions in Three-Dimensional Models.

Authors:  David A Kukla; Alexandra L Crampton; David K Wood; Salman R Khetani
Journal:  Gene Expr       Date:  2020-04-14

8.  Role of Organic Solute Transporter Alpha/Beta in Hepatotoxic Bile Acid Transport and Drug Interactions.

Authors:  James J Beaudoin; Jacqueline Bezençon; Noora Sjöstedt; John K Fallon; Kim L R Brouwer
Journal:  Toxicol Sci       Date:  2020-07-01       Impact factor: 4.849

9.  Effects of Endogenous PPAR Agonist Nitro-Oleic Acid on Metabolic Syndrome in Obese Zucker Rats.

Authors:  Haiping Wang; Haiying Liu; Zhanjun Jia; Guangju Guan; Tianxin Yang
Journal:  PPAR Res       Date:  2010-07-05       Impact factor: 4.964

Review 10.  Advancement of structure-activity relationship of multidrug resistance-associated protein 2 interactions.

Authors:  Li Xing; Yiding Hu; Yurong Lai
Journal:  AAPS J       Date:  2009-06-03       Impact factor: 4.009

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