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Lupin protein isolate versus casein modifies cholesterol excretion and mRNA expression of intestinal sterol transporters in a pig model.


ABSTRACT: BACKGROUND:Lupin proteins exert hypocholesterolemic effects in man and animals, although the underlying mechanism remains uncertain. Herein we investigated whether lupin proteins compared to casein modulate sterol excretion and mRNA expression of intestinal sterol transporters by use of pigs as an animal model with similar lipid metabolism as humans, and cellular cholesterol-uptake by Caco-2 cells. METHODS:Two groups of pigs were fed cholesterol-containing diets with either 230 g/kg of lupin protein isolate from L. angustifolius or 230 g/kg casein, for 4 weeks. Faeces were collected quantitatively over a 5 d period for analysis of neutral sterols and bile acids by gas chromatographically methods. The mRNA abundances of intestinal lipid transporters were analysed by real-time RT-PCR. Cholesterol-uptake studies were performed with Caco-2 cells that were incubated with lupin conglutin ?, phytate, ezetimibe or albumin in the presence of labelled [4-14C]-cholesterol. RESULTS:Pigs fed the lupin protein isolate revealed lower cholesterol concentrations in total plasma, LDL and HDL than pigs fed casein (P?

SUBMITTER: Radtke J 

PROVIDER: S-EPMC3922606 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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Lupin protein isolate versus casein modifies cholesterol excretion and mRNA expression of intestinal sterol transporters in a pig model.

Radtke Juliane J   Geissler Stefanie S   Schutkowski Alexandra A   Brandsch Corinna C   Kluge Holger H   Duranti Marcello M MM   Keller Sylvia S   Jahreis Gerhard G   Hirche Frank F   Stangl Gabriele I GI  

Nutrition & metabolism 20140203 1


<h4>Background</h4>Lupin proteins exert hypocholesterolemic effects in man and animals, although the underlying mechanism remains uncertain. Herein we investigated whether lupin proteins compared to casein modulate sterol excretion and mRNA expression of intestinal sterol transporters by use of pigs as an animal model with similar lipid metabolism as humans, and cellular cholesterol-uptake by Caco-2 cells.<h4>Methods</h4>Two groups of pigs were fed cholesterol-containing diets with either 230 g/  ...[more]

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