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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1998-1-6
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pubmed:abstractText |
The effects of partially hydrolyzed, nonviscous, guar gum (PHGG) on cholesterol metabolism and digestive balance have been compared with those of native guar gum (GUAR) in rats adapted to 0.4% cholesterol diets. Both types of guar gum elicited acidic fermentations in the large intestine, but only GUAR effectively lowered plasma cholesterol (P < 0.001), chiefly in the triglyceride-rich lipoprotein fraction. The biliary bile acid excretion was significantly enhanced in rats fed GUAR (P < 0.05), as well as the intestinal and cecal bile acid pool (P < 0.001). In rats fed GUAR and to a lesser extent in those fed PHGG, the fecal excretion of bile acids and neutral sterol was higher than in controls (P < 0.01). The digestive balance (cholesterol intake-steroid excretion) was positive in control rats (+47 mumol/d), whereas it was negative in rats fed GUAR (-20 mumol/d), which could involve a higher rate of endogenous cholesterol synthesis. In rats fed PHGG, the steroid balance remained slightly positive. Liver 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase activity was very low (22 pmol/min/mg protein), owing to cholesterol supplementation, in control rats or in rats fed PHGG, whereas it was markedly higher (+463%) in rats fed GUAR. In conclusion, even if PHGG does alter some parameters of the enterohepatic cycle of cholesterol and bile acids, its effects are not sufficient to elicit a significant cholesterol-lowering effect. The intestinal (ileal or cecal) reabsorption of bile acids was not reduced, but rather increased, by GUAR; nevertheless the intestinal capacities of reabsorption were overwhelmed by the enlargement of the digestive pool of bile acids. In the present model, induction of HMG-CoA reductase probably takes place in the presence of elevated portal bile acid concentrations.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anticholesteremic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Bile Acids and Salts,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol,
http://linkedlifedata.com/resource/pubmed/chemical/Dietary Fats,
http://linkedlifedata.com/resource/pubmed/chemical/Galactans,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl CoA Reductases,
http://linkedlifedata.com/resource/pubmed/chemical/Lipids,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Mannans,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Gums,
http://linkedlifedata.com/resource/pubmed/chemical/guar gum
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0024-4201
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
953-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9307936-Animals,
pubmed-meshheading:9307936-Anticholesteremic Agents,
pubmed-meshheading:9307936-Bile,
pubmed-meshheading:9307936-Bile Acids and Salts,
pubmed-meshheading:9307936-Body Weight,
pubmed-meshheading:9307936-Cecum,
pubmed-meshheading:9307936-Cholesterol,
pubmed-meshheading:9307936-Dietary Fats,
pubmed-meshheading:9307936-Feces,
pubmed-meshheading:9307936-Galactans,
pubmed-meshheading:9307936-Hydrogen-Ion Concentration,
pubmed-meshheading:9307936-Hydroxymethylglutaryl CoA Reductases,
pubmed-meshheading:9307936-Intestinal Absorption,
pubmed-meshheading:9307936-Lipids,
pubmed-meshheading:9307936-Lipoproteins,
pubmed-meshheading:9307936-Liver,
pubmed-meshheading:9307936-Male,
pubmed-meshheading:9307936-Mannans,
pubmed-meshheading:9307936-Organ Size,
pubmed-meshheading:9307936-Plant Gums,
pubmed-meshheading:9307936-Rats,
pubmed-meshheading:9307936-Rats, Wistar
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pubmed:year |
1997
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pubmed:articleTitle |
The cholesterol-lowering effect of guar gum is not the result of a simple diversion of bile acids toward fecal excretion.
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pubmed:affiliation |
Laboratoire des Maladies Métaboliques et Micronutriments, INRA de Clermont-Ferrand/Theix, Ceyrat, France.
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pubmed:publicationType |
Journal Article
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