Literature DB >> 9202089

Genetic variation in cholesterol absorption efficiency among inbred strains of mice.

C P Carter1, P N Howles, D Y Hui.   

Abstract

The initial study utilized the outbred Black Swiss, the inbred 129/SvEv and their hybrid mice to test for possible genetic difference in cholesterol absorption efficiency. Female mice (10-12 wk old) were fed a lipid test meal containing [3H]cholesterol and beta-[14C]sitosterol by stomach tube. The amount of [3H]cholesterol excreted in the feces was determined as nonabsorbed cholesterol and was normalized based on the recovery of the nonabsorbable beta-[14C]sitosterol. The Black Swiss mice absorbed significantly less cholesterol than the 129/SvEv mice within a 24-h period. Cholesterol absorption efficiency of the hybrid mice varied widely and did not segregate with either parental group. Differences in cholesterol absorption efficiency were also observed among six different inbred strains of mice fed either a basal low fat diet or a high fat/high cholesterol diet for 3 wk. Cholesterol absorption efficiency did not differ among DBA/2, C57BL/6, C3H/He, BALB/c and AKR/J mice under basal dietary conditions. However, cholesterol absorption was significantly lower in the DBA/2 mice than in C57BL/6 and C3H/He mice after mice were fed a high fat/high cholesterol diet. Cholesterol absorption by the C57L/J mice did not differ from that of C57BL/6, C3H/He, BALB/c and AKR/J mice under basal diet conditions, but was significantly lower when mice were fed a high fat/high cholesterol diet. Cholesterol absorption efficiency differed between DBA/2 and C57L/J mice under both dietary conditions. These results suggest that cholesterol absorption is controlled by multiple genetic factors.

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Year:  1997        PMID: 9202089     DOI: 10.1093/jn/127.7.1344

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  16 in total

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2.  Expression of liver plasma membrane transporters in gallstone-susceptible and gallstone-resistant mice.

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3.  Molecular cloning, genomic organization, genetic variations, and characterization of murine sterolin genes Abcg5 and Abcg8.

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4.  Pancreatic lipase/colipase-mediated triacylglycerol hydrolysis is required for cholesterol transport from lipid emulsions to intestinal cells.

Authors:  S C Young; D Y Hui
Journal:  Biochem J       Date:  1999-05-01       Impact factor: 3.857

Review 5.  Animal models of atherosclerosis.

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6.  Variability of the intestinal uptake of lipids is genetically determined in mice.

Authors:  M Keelan; D Y Hui; G Wild; M T Clandinin; A B Thomson
Journal:  Lipids       Date:  2000-08       Impact factor: 1.880

7.  Mouse strain-dependent variation in obesity and glucose homeostasis in response to high-fat feeding.

Authors:  M K Montgomery; N L Hallahan; S H Brown; M Liu; T W Mitchell; G J Cooney; N Turner
Journal:  Diabetologia       Date:  2013-02-20       Impact factor: 10.122

8.  Biliary cholesterol excretion: a novel mechanism that regulates dietary cholesterol absorption.

Authors:  E Sehayek; J G Ono; S Shefer; L B Nguyen; N Wang; A K Batta; G Salen; J D Smith; A R Tall; J L Breslow
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-18       Impact factor: 11.205

9.  Transcriptional profiles of leukocyte populations provide a tool for interpreting gene expression patterns associated with high fat diet in mice.

Authors:  William R Swindell; Andrew Johnston; Johann E Gudjonsson
Journal:  PLoS One       Date:  2010-07-29       Impact factor: 3.240

10.  Differing rates of cholesterol absorption among inbred mouse strains yield differing levels of HDL-cholesterol.

Authors:  Timothy J Sontag; Bijoy Chellan; Godfrey S Getz; Catherine A Reardon
Journal:  J Lipid Res       Date:  2013-06-27       Impact factor: 5.922

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