Literature DB >> 7351873

Oral contraceptives raise the cholesterol saturation of bile by increasing biliary cholesterol secretion.

L J Bennion, D M Mott, B V Howard.   

Abstract

To discover the mechanism by which oral contraceptives increase the level of cholesterol saturation of human bile, we measured biliary lipid secretion rates, gallbladder and hepatic bile lipid composition, bile acid pool size, bile acid composition, and plasma lipoprotein levels in five healthy women during routine oral contraceptive treatment and again during normal menstrual cycles on no medication. The molar percent cholesterol in both gallbladder and hepatic bile was higher in every subject while taking oral contraceptives (p less than .02). Oral contraceptive usage was accompanied by a significant enhancement of biliary cholesterol secretion (65 versus 46 mg/hr, p less than .01), but there was no significant change in bile acid or phospholipid secretion, total bile acid pool size, or bile acid composition. These findings indicate that oral contraceptive usage increases biliary cholesterol secretion, thereby raising the level of cholesterol saturation of bile and predisposing to cholesterol precipitation and gallstone formation.

Entities:  

Keywords:  Biology; Clinical Research; Contraception; Contraceptive Methods--side effects; Family Planning; Lipid Metabolic Effects; Lipids; Oral Contraceptives--side effects; Physiology; Research Methodology

Mesh:

Substances:

Year:  1980        PMID: 7351873     DOI: 10.1016/0026-0495(80)90092-x

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  16 in total

1.  Estrogen induces two distinct cholesterol crystallization pathways by activating ERα and GPR30 in female mice.

Authors:  Ornella de Bari; Tony Y Wang; Min Liu; Piero Portincasa; David Q-H Wang
Journal:  J Lipid Res       Date:  2015-07-07       Impact factor: 5.922

Review 2.  Defective acid base regulation by the gall bladder epithelium and its significance for gall stone formation.

Authors:  J N Plevris; I A Bouchier
Journal:  Gut       Date:  1995-07       Impact factor: 23.059

3.  Effect of a synthetic androgen on biliary lipid secretion in the female hamster.

Authors:  A Ohshima; B I Cohen; N Ayyad; E H Mosbach
Journal:  Lipids       Date:  1996-08       Impact factor: 1.880

4.  Effect of synthetic oestrogens and progestagens in oral contraceptives on bile lipid composition.

Authors:  R H Down; M J Whiting; J M Watts; W Jones
Journal:  Gut       Date:  1983-03       Impact factor: 23.059

5.  Oral contraceptives, pregnancy, and endogenous oestrogen in gall stone disease--a case-control study.

Authors:  R K Scragg; A J McMichael; R F Seamark
Journal:  Br Med J (Clin Res Ed)       Date:  1984-06-16

6.  Mechanisms of gallstone formation in women. Effects of exogenous estrogen (Premarin) and dietary cholesterol on hepatic lipid metabolism.

Authors:  G T Everson; C McKinley; F Kern
Journal:  J Clin Invest       Date:  1991-01       Impact factor: 14.808

Review 7.  Drug-induced cholestasis.

Authors:  H J Zimmerman; J H Lewis
Journal:  Med Toxicol       Date:  1987 Mar-Apr

8.  Gallbladder and small intestinal regulation of biliary lipid secretion during intraduodenal infusion of standard stimuli.

Authors:  G T Everson; M J Lawson; C McKinley; R Showalter; F Kern
Journal:  J Clin Invest       Date:  1983-03       Impact factor: 14.808

Review 9.  Drug-induced gallbladder disease. Incidence, aetiology and management.

Authors:  P P Michielsen; H Fierens; Y M Van Maercke
Journal:  Drug Saf       Date:  1992 Jan-Feb       Impact factor: 5.606

10.  The deletion of the estrogen receptor α gene reduces susceptibility to estrogen-induced cholesterol cholelithiasis in female mice.

Authors:  Ornella de Bari; Helen H Wang; Piero Portincasa; Min Liu; David Q-H Wang
Journal:  Biochim Biophys Acta       Date:  2015-07-30
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