Literature DB >> 12479586

Intestinal lipid absorption is not affected in CD36 deficient mice.

Jeltje R Goudriaan1, Vivian E H Dahlmans, Maria Febbraio, Bas Teusink, Johannes A Romijn, Louis M Havekes, Peter J Voshol.   

Abstract

Increasing evidence has implicated the membrane protein CD36 (or fatty acid translocase, FAT) to be involved in high affinity fatty acid uptake. CD36 is expressed in tissues active in fatty acid metabolism, like adipose tissue and skeletal and cardiac muscle, but also in intestine. CD36 is localized in the intestine mainly in the jejunal villi, where it is confined to enterocyte apical membrane. The aim was to determine the role of CD36 in intestinal lipid absorption. Lipid absorption was determined by administering 3H-labeled triolein and 14C-labeled palmitic acid as an olive oil bolus by intragastric gavage and determine appearance of 3H and 14C label in plasma, after blocking lipolysis by i.v. injections of Triton WR 1339. Surprisingly, no differences in plasma appearance of 3H-label or 14C-label were observed in CD36(-/-) mice compared to wild type controls. These results suggest that CD36 does not play a role in intestinal lipid absorption after an acute lipid load.

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Year:  2002        PMID: 12479586

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  16 in total

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Journal:  J Biol Chem       Date:  1999-07-02       Impact factor: 5.157

5.  Glycoprotein IV mediates thrombospondin-dependent platelet-monocyte and platelet-U937 cell adhesion.

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Authors:  G Endemann; L W Stanton; K S Madden; C M Bryant; R T White; A A Protter
Journal:  J Biol Chem       Date:  1993-06-05       Impact factor: 5.157

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Journal:  J Biol Chem       Date:  1993-08-25       Impact factor: 5.157

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6.  A uroguanylin-GUCY2C endocrine axis regulates feeding in mice.

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8.  CD36 deficiency impairs intestinal lipid secretion and clearance of chylomicrons from the blood.

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