Literature DB >> 8582435

Biliary lipids, lithogenic index and biliary drug concentrations during etofibrate and bezafibrate treatment.

R Raedsch1, J Plachky, N Wolf, G Simonis.   

Abstract

Hypolipidemic drugs like etofibrate and bezafibrate may induce lithogenic bile and increase the risk of gallstone formation. In this study, biliary lipids, lithogenic index and biliary drug concentrations were investigated in 6 hyperlipidemic patients after cholecystectomy. Patients were treated once daily for 5 days with either 500 mg/day etofibrate or 400 mg/day bezafibrate. Hepatic bile was collected for 6 days via T-drainage in 4 hourly aliquots. In the patients treated with etofibrate, the range of the lithogenic index remained stable with 0.89-1.69 before and 0.78-1.51 after 5 day drug therapy. In the bezafibrate group, the range of the lithogenic index rose from 0.81-1.40 to 1.26-1.66 mainly as a result of an increase of biliary cholesterol concentrations. Biliary drug concentrations were substantially higher under bezafibrate treatment than under etofibrate treatment. In conclusion, the fibrate drugs, etofibrate and bezafibrate, are different with regard to lithogenicity of bile and extent of biliary excretion. The safety profile of etofibrate may be preferably compared to other fibrate drugs.

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Year:  1995        PMID: 8582435     DOI: 10.1007/BF03226364

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  10 in total

1.  The effect of etofibrate on cholesterol and bile acid metabolism in the hamster.

Authors:  E De Fabiani; M Crestani; B Malavasi; M Del Puppo; F Farina; C Armocida; S Bellentani; G Quack; E Bosisio
Journal:  Pharmacol Res       Date:  1989 Sep-Oct       Impact factor: 7.658

2.  Influence of etofibrate on low density lipoprotein metabolism.

Authors:  J J Series; M J Caslake; C Kilday; A Cruickshank; T Demant; C J Packard; J Shepherd
Journal:  Atherosclerosis       Date:  1988-02       Impact factor: 5.162

3.  Ursodeoxycholic acid versus chenodeoxycholic acid. Comparison of their effects on bile acid and bile lipid composition in patients with cholesterol gallstones.

Authors:  A Stiehl; P Czygan; B Kommerell; H J Weis; K H Holtermüller
Journal:  Gastroenterology       Date:  1978-12       Impact factor: 22.682

Review 4.  Clinical pharmacokinetics of hypolipidaemic drugs.

Authors:  R Gugler
Journal:  Clin Pharmacokinet       Date:  1978 Nov-Dec       Impact factor: 6.447

5.  Letter: A simple calculation of the lithogenic index of bile: expressing biliary lipid composition on rectangular coordinates.

Authors:  P J Thomas; A F Hofmann
Journal:  Gastroenterology       Date:  1973-10       Impact factor: 22.682

6.  The solubility of cholesterol in aqueous solutions of bile salts and lecithin.

Authors:  F G Hegardt; H Dam
Journal:  Z Ernahrungswiss       Date:  1971-04

Review 7.  Effects of fibric acid derivatives on biliary lipid composition.

Authors:  R H Palmer
Journal:  Am J Med       Date:  1987-11-27       Impact factor: 4.965

Review 8.  Adverse effects of hypolipidaemic drugs.

Authors:  L C Knodel; R L Talbert
Journal:  Med Toxicol       Date:  1987 Jan-Feb

Review 9.  Bezafibrate. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hyperlipidaemia.

Authors:  J P Monk; P A Todd
Journal:  Drugs       Date:  1987-06       Impact factor: 9.546

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Authors:  R T Holzbach; M Marsh; M Olszewski; K Holan
Journal:  J Clin Invest       Date:  1973-06       Impact factor: 14.808

  10 in total
  4 in total

Review 1.  How well tolerated are lipid-lowering drugs?

Authors:  B Tomlinson; P Chan; W Lan
Journal:  Drugs Aging       Date:  2001       Impact factor: 3.923

Review 2.  Bezafibrate. An update of its pharmacology and use in the management of dyslipidaemia.

Authors:  K L Goa; L B Barradell; G L Plosker
Journal:  Drugs       Date:  1996-11       Impact factor: 9.546

3.  The inhibition of the human cholesterol 7alpha-hydroxylase gene (CYP7A1) promoter by fibrates in cultured cells is mediated via the liver x receptor alpha and peroxisome proliferator-activated receptor alpha heterodimer.

Authors:  G Franck Gbaguidi; Luis B Agellon
Journal:  Nucleic Acids Res       Date:  2004-02-11       Impact factor: 16.971

Review 4.  A reappraisal of the risks and benefits of treating to target with cholesterol lowering drugs.

Authors:  Venkata M Alla; Vrinda Agrawal; Andrew DeNazareth; Syed Mohiuddin; Sudha Ravilla; Marc Rendell
Journal:  Drugs       Date:  2013-07       Impact factor: 9.546

  4 in total

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