Literature DB >> 4727464

Regulation of cholesterol metabolism in the dog. I. Effects of complete bile diversion and of cholesterol feeding on absorption, synthesis, accumulation, and excretion rates measured during life.

D Pertsemlidis, E H Kirchman, E H Ahrens.   

Abstract

Six adult pedigreed dogs were studied as long as 3 yr in order to determine the effects of cholesterol feeding and of bile diversion on absorption, synthesis, and storage of cholesterol. These measurements were based on cholesterol balance and isotope kinetic studies. In the six dogs fed a "cholesterol-free" diet with their enterohepatic circulations undisturbed, the rate of cholesterol synthesis ranged from 225 to 508 mg/day (mean 325 mg/day or 12.4 mg/kg/day). In two dogs studied subsequently on cholesterol-containing diets, absorption of cholesterol averaged 81% (range 71-94%) on a dietary intake of 0.5 g/day; on high cholesterol intakes (2.7-3.0 g/day) the rate of absorption dropped to 43-51% of daily intake, but the absolute amounts absorbed were increased. Feeding of cholesterol resulted in acceleration of bile acid formation and excretion, as well as nearly total inhibition of cholesterol synthesis. These two compensatory mechanisms were sufficient to maintain zero balance of cholesterol in the face of a high cholesterol intake. Plasma cholesterol concentrations in the two dogs increased by 37 and 44%. In two other dogs bile was completely diverted into the urinary system for nearly 2 yr. When these dogs were studied on a cholesterol-free diet, the sum of acidic steroids excreted daily in urine plus neutral steroids excreted in feces was seven times as high as before the operation. Since these massive excretory losses could not have been sustained by mobilization from tissue cholesterol pools, and since the rate of disappearance of [4-(14)C]cholesterol from the plasma after single intravenous injection was greatly increased after complete biliary diversion, total daily synthesis of cholesterol must have been greatly accelerated, for synthesis was totally unsuppressed. The increased output of fecal neutral steroids could be the result of transfer of plasma cholesterol across the gut wall or due to increased synthesis in the gut. Plasma cholesterol levels were reduced in these two dogs by 20 and 27%, and triglycerides decreased by 36 and 43%. Accumulation of cholesterol in body pools in the cholesterol-fed dogs appeared to have been prevented, according to antemortem measurements: increased absorption of dietary cholesterol was exactly balanced by suppression of cholesterol synthesis and enhanced bile acid excretion. In the bile-shunted animals, depletion of tissue stores of cholesterol could not be predicted by antemortem measurements.

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Year:  1973        PMID: 4727464      PMCID: PMC333040          DOI: 10.1172/JCI107424

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  17 in total

1.  QUANTITATIVE ISOLATION AND GAS--LIQUID CHROMATOGRAPHIC ANALYSIS OF TOTAL DIETARY AND FECAL NEUTRAL STEROIDS.

Authors:  T A MIETTINEN; E H AHRENS; S M GRUNDY
Journal:  J Lipid Res       Date:  1965-07       Impact factor: 5.922

2.  QUANTITATIVE ISOLATION AND GAS--LIQUID CHROMATOGRAPHIC ANALYSIS OF TOTAL FECAL BILE ACIDS.

Authors:  S M GRUNDY; E H AHRENS; T A MIETTINEN
Journal:  J Lipid Res       Date:  1965-07       Impact factor: 5.922

3.  The origin of serum cholesterol in the rat; diet versus synthesis.

Authors:  M D MORRIS; I L CHAIKOFF; J M FELTS; S ABRAHAM; N O FANSAH
Journal:  J Biol Chem       Date:  1957-02       Impact factor: 5.157

4.  Studies on the influence of dietary cholesterol on cholesterol metabolism in the isotopic steady state in man.

Authors:  J D Wilson; C A Lindsey
Journal:  J Clin Invest       Date:  1965-11       Impact factor: 14.808

Review 5.  Regulation of cholesterol metabolism. I.

Authors:  J M Dietschy; J D Wilson
Journal:  N Engl J Med       Date:  1970-05-14       Impact factor: 91.245

6.  Usefulness of chromic oxide as an internal standard for balance studies in formula-fed patients and for assessment of colonic function.

Authors:  J Davignon; W J Simmonds; E H Ahrens
Journal:  J Clin Invest       Date:  1968-01       Impact factor: 14.808

7.  Effects of dietary cholesterol on the regulation of total body cholesterol in man.

Authors:  E Quintão; S M Grundy; E H Ahrens
Journal:  J Lipid Res       Date:  1971-03       Impact factor: 5.922

8.  An evaluation of four methods for measuring cholesterol absorption by the intestine in man.

Authors:  E Quintão; S M Grundy; E H Ahrens
Journal:  J Lipid Res       Date:  1971-03       Impact factor: 5.922

9.  Improved estimation of body masses and turnover of cholesterol by computerized input--output analysis.

Authors:  P Samuel; S Lieberman
Journal:  J Lipid Res       Date:  1973-03       Impact factor: 5.922

10.  Dietary beta-sitosterol as an internal standard to correct for cholesterol losses in sterol balance studies.

Authors:  S M Grundy; E H Ahrens; G Salen
Journal:  J Lipid Res       Date:  1968-05       Impact factor: 5.922

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  18 in total

Review 1.  A new framework for reverse cholesterol transport: non-biliary contributions to reverse cholesterol transport.

Authors:  Ryan-E Temel; J-Mark Brown
Journal:  World J Gastroenterol       Date:  2010-12-21       Impact factor: 5.742

Review 2.  From blood to gut: direct secretion of cholesterol via transintestinal cholesterol efflux.

Authors:  Carlos L J Vrins
Journal:  World J Gastroenterol       Date:  2010-12-21       Impact factor: 5.742

Review 3.  A new model of reverse cholesterol transport: enTICEing strategies to stimulate intestinal cholesterol excretion.

Authors:  Ryan E Temel; J Mark Brown
Journal:  Trends Pharmacol Sci       Date:  2015-04-27       Impact factor: 14.819

Review 4.  Does Dietary Cholesterol Matter?

Authors:  Scott M Grundy
Journal:  Curr Atheroscler Rep       Date:  2016-11       Impact factor: 5.113

5.  Biliary sterol secretion is not required for macrophage reverse cholesterol transport.

Authors:  Ryan E Temel; Janet K Sawyer; Liqing Yu; Caleb Lord; Chiara Degirolamo; Allison McDaniel; Stephanie Marshall; Nanping Wang; Ramesh Shah; Lawrence L Rudel; J Mark Brown
Journal:  Cell Metab       Date:  2010-07-07       Impact factor: 27.287

Review 6.  Biliary and nonbiliary contributions to reverse cholesterol transport.

Authors:  Ryan E Temel; J Mark Brown
Journal:  Curr Opin Lipidol       Date:  2012-04       Impact factor: 4.776

7.  Evaluation of chromic oxide, glycerol triether, and beta-sitosterol as fecal flow markers in two species of nonhuman primates.

Authors:  R W St Clair; N D Lehner; T E Hamm
Journal:  Lipids       Date:  1975-01       Impact factor: 1.880

8.  Prevention of induced atherosclerosis by diversion of bile or blockade of intestinal lymphatics in dogs.

Authors:  P J Wilk; R C Karipineni; D Pertsemlidis; C A Danese
Journal:  Ann Surg       Date:  1976-04       Impact factor: 12.969

9.  Targeted depletion of hepatic ACAT2-driven cholesterol esterification reveals a non-biliary route for fecal neutral sterol loss.

Authors:  J Mark Brown; Thomas A Bell; Heather M Alger; Janet K Sawyer; Thomas L Smith; Kathryn Kelley; Ramesh Shah; Martha D Wilson; Matthew A Davis; Richard G Lee; Mark J Graham; Rosanne M Crooke; Lawrence L Rudel
Journal:  J Biol Chem       Date:  2008-02-14       Impact factor: 5.157

10.  Regulation of cholesterol metabolism in the dog. II. Effects of complete bile diversion and of cholesterol feeding on pool sizes of tissue cholesterol measured at autopsy.

Authors:  D Pertsemlidis; E H Kirchman; E H Ahrens
Journal:  J Clin Invest       Date:  1973-09       Impact factor: 14.808

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