Literature DB >> 6838687

Influence of fenofibrate on cellular and subcellular liver structure in hyperlipidemic patients.

S Blümcke, W Schwartzkopff, H Lobeck, N A Edmondson, D E Prentice, G F Blane.   

Abstract

The administration of lipid-lowering drugs to rodents, notably those related to clofibrate, rapidly provokes a hepatic response characterized by hepatomegaly, proliferation of smooth endoplasmic reticulum and proliferation of peroxisomes in hepatocytes. In some studies hepatocellular carcinoma has been found in rats or mice exposed for their entire life-span to high dose levels of various fibrates. In the present study liver biopsy samples were obtained from 38 hyperlipidemic patients, 28 of whom had been receiving fenofibrate for between 2 months and approximately 3 years (mean values: males 1.79, females 1.98 years). The remaining 10 patients had never been treated with a lipid-lowering drug. Examination of the biopsy samples by a variety of optical techniques and by electron microscopy failed to reveal any difference between the groups. Peroxisomes were relatively rare, there being no evidence of the clear proliferation seen in rodent studies. Other microscopic features of interest were some variation of nuclear size, mitochondria containing paracrystalline inclusions, dilated endoplasmic reticulum associated with reduced amounts of rough endoplasmic reticulum, and the presence of lipid droplets in the liver cells. However, these variations from normal were in general not much more apparent in samples from the fenofibrate-treated patients than in the untreated group. Light- and electron-microscopic observations did not suggest liver intoxication or a carcinogenic pattern.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6838687     DOI: 10.1016/0021-9150(83)90169-7

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  16 in total

1.  Comparative induction of cytochrome P450IVA1 and peroxisome proliferation by ciprofibrate in the rat and marmoset.

Authors:  J M Makowska; F W Bonner; G G Gibson
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

Review 2.  Fenofibrate. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in dyslipidaemia.

Authors:  J A Balfour; D McTavish; R C Heel
Journal:  Drugs       Date:  1990-08       Impact factor: 9.546

Review 3.  Fibrates, glitazones, and peroxisome proliferator-activated receptors.

Authors:  Fanny Lalloyer; Bart Staels
Journal:  Arterioscler Thromb Vasc Biol       Date:  2010-05       Impact factor: 8.311

Review 4.  Use of fibrates in the metabolic syndrome: A review.

Authors:  Kate E Shipman; Richard C Strange; Sudarshan Ramachandran
Journal:  World J Diabetes       Date:  2016-03-10

Review 5.  Secondary alterations of human hepatocellular peroxisomes.

Authors:  D De Craemer
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

6.  Fatty acid metabolism in hepatocytes cultured with hypolipidaemic drugs. Role of carnitine.

Authors:  P Gerondaes; K G Alberti; L Agius
Journal:  Biochem J       Date:  1988-07-01       Impact factor: 3.857

Review 7.  Peroxisome proliferator-activated receptor-alpha and liver cancer: where do we stand?

Authors:  Jeffrey M Peters; Connie Cheung; Frank J Gonzalez
Journal:  J Mol Med (Berl)       Date:  2005-06-23       Impact factor: 4.599

8.  Induction of hepatic peroxisome proliferation in nonrodent species, including primates.

Authors:  J K Reddy; N D Lalwani; S A Qureshi; M K Reddy; C M Moehle
Journal:  Am J Pathol       Date:  1984-01       Impact factor: 4.307

Review 9.  Role of peroxisome proliferators-activated receptors in the pathogenesis and treatment of nonalcoholic fatty liver disease.

Authors:  Eric R Kallwitz; Alan McLachlan; Scott J Cotler
Journal:  World J Gastroenterol       Date:  2008-01-07       Impact factor: 5.742

Review 10.  A reexamination of the PPAR-alpha activation mode of action as a basis for assessing human cancer risks of environmental contaminants.

Authors:  Kathryn Z Guyton; Weihsueh A Chiu; Thomas F Bateson; Jennifer Jinot; Cheryl Siegel Scott; Rebecca C Brown; Jane C Caldwell
Journal:  Environ Health Perspect       Date:  2009-05-15       Impact factor: 9.031

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.