Literature DB >> 2086701

Dietary cholesterol absorption, and sterol and bile acid excretion in hypercholesterolemia-resistant white rabbits.

M L Overturf1, S A Smith, A M Gotto, J D Morrisett, T Tewson, J Poorman, D S Loose-Mitchell.   

Abstract

The New Zealand white (NZW) rabbit fed a 0.1% cholesterol-enriched diet (CD) typically responds (normoresponsive, NR) by quickly developing hypercholesterolemia. To study the underlying mechanisms responsible for the widespread phenomenon of inter-individual variability of response to dietary cholesterol, a unique hypercholesterolemia-resistant (RT) rabbit model was developed. These animals were utilized to investigate selected potential mechanisms that might enable the RT animal to compensate for dietary cholesterol overload. When rabbits were fed the low-cholesterol stock diet, there was no significant difference in the plasma cholesterol concentrations of the NR and the RT animals. However, a significant rise was observed in the NR rabbits within 1 month of their being placed on the cholesterol-enriched diet; the plasma cholesterol concentration of the RT animals was not affected. During consumption of the cholesterol diet the cholesterol absorption rate was somewhat greater in the NR rabbits (P less than 0.05), whereas intestinal transit times and the fecal excretion of neutral steroids were substantially the same in both groups. In contrast, the fecal bile acid excretion of the RT animals was more than twice as great (P less than 0.0001) as that of the NR animals. We conclude that the response to dietary cholesterol is a heritable trait in these rabbits and that, although less dietary cholesterol was absorbed by the RT animals, it appears that a major mechanism controlling plasma cholesterol levels involves the rate of conversion of cholesterol to bile acids and their subsequent excretion.

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Year:  1990        PMID: 2086701

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  5 in total

1.  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

2.  Complex genetic control of HDL levels in mice in response to an atherogenic diet. Coordinate regulation of HDL levels and bile acid metabolism.

Authors:  D Machleder; B Ivandic; C Welch; L Castellani; K Reue; A J Lusis
Journal:  J Clin Invest       Date:  1997-03-15       Impact factor: 14.808

3.  Resistance to dietary-induced hypercholesterolemia exhibited by a unique strain of New Zealand white rabbits.

Authors:  M L Overturf; R A Buck; D S Loose-Mitchell
Journal:  Tex Heart Inst J       Date:  1994

4.  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

5.  Bile acid and very low density lipoprotein production by cultured hepatocytes from hypo- or hyperresponsive rabbits fed cholesterol.

Authors:  E A Podrez; V A Kosykh; Y V Lakeev; E I Kosenkov; E T Mambetisaeva; V S Repin; V N Smirnov; T A Miettinen
Journal:  Lipids       Date:  1993-08       Impact factor: 1.880

  5 in total

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