Literature DB >> 185488

Changes in plasma triglyceride metabolism during withdrawal of bile.

P J Nestel, S M Grundy.   

Abstract

The relationship between bile acid turnover and plasma triglyceride metabolism was examined in a group of seven moderately overweight and hypertriglyceridemic men. Bile acid synthesis was stimulated by the continuous aspiration of duodenal contents so that 150% of the bile acid pool was removed in 18 hr. In comparison with the average concentration of very low density lipoprotein triglyceride (VLDL-TG) during a preceding 8-10 hr control period, bile withdrawal led to an increase in VLDL-TG of 34%, 43%, 32%, 14%, 26%, 14%, and 8% (mean +24%) in the seven men. In control studies performed on another day the mean change over a similar period of time, but without bile withdrawal, was +1% (p less than 0.01). The kinetics of VLDL triglyceride were studied in some of the subjects by analyzing the triglyceride specific radioactivity curves following injections of radiolabelled glycerol. In control studies of 26 hr duration the curves were resolved into two apparent exponential functions, the second part of the curve appearing between 15 and 18 hr after pulse-labeling. During bile withdrawal, the second apparent exponential developed sooner, within 4 hr of beginning the aspiration and coincided with the rise in triglyceride concentration. The fractional rate of the second exponential was at least as fast during bile withdrawal as during the control period despite the increase in VLDL-TG pool size, suggesting that the turnover of triglyceride was higher at a time when bile acid production was being stimulated.

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Year:  1976        PMID: 185488     DOI: 10.1016/s0026-0495(76)80009-1

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


  8 in total

1.  Bile acid sequestrants: mechanisms of action on bile acid and cholesterol metabolism.

Authors:  K Einarsson; S Ericsson; S Ewerth; E Reihnér; M Rudling; D Ståhlberg; B Angelin
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

2.  Bile acid metabolism in hereditary forms of hypertriglyceridemia: evidence for an increased synthesis rate in monogenic familial hypertriglyceridemia.

Authors:  B Angelin; K S Hershon; J D Brunzell
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

3.  Concomitant increase in hepatic triacylglycerol biosynthesis and cytosolic fatty-acid-binding-protein content after feeding rats with a cholestyramine-containing diet.

Authors:  H J Kempen; J F Glatz; J de Lange; J H Veerkamp
Journal:  Biochem J       Date:  1983-11-15       Impact factor: 3.857

Review 4.  Endocrine functions of bile acids.

Authors:  Sander M Houten; Mitsuhiro Watanabe; Johan Auwerx
Journal:  EMBO J       Date:  2006-03-16       Impact factor: 11.598

Review 5.  Bile acids as regulatory molecules.

Authors:  Phillip B Hylemon; Huiping Zhou; William M Pandak; Shunlin Ren; Gregorio Gil; Paul Dent
Journal:  J Lipid Res       Date:  2009-04-03       Impact factor: 5.922

6.  Non-alcoholic Fatty liver disease: the bile Acid-activated farnesoid x receptor as an emerging treatment target.

Authors:  Michael Fuchs
Journal:  J Lipids       Date:  2011-12-07

Review 7.  Optimal lipid modification: the rationale for combination therapy.

Authors:  James M Backes; Cheryl A Gibson; Patricia A Howard
Journal:  Vasc Health Risk Manag       Date:  2005

Review 8.  Bile acids and sphingosine-1-phosphate receptor 2 in hepatic lipid metabolism.

Authors:  Eric Kwong; Yunzhou Li; Phillip B Hylemon; Huiping Zhou
Journal:  Acta Pharm Sin B       Date:  2015-02-09       Impact factor: 11.413

  8 in total

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