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J Nutr ; 133(3): 752-7, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12612148

ABSTRACT

The aim of the present study was to determine the effects of dietary proteins on the oxidation of dietary carbohydrate and lipids in type II diabetic mice. KK-A(y) strain mice were provided free access to a high fat diet (30% of energy as fat) for an initial 4-wk period to induce diabetes. To reduce body weight gain, the mice were subsequently fed restrictive isoenergetic and isonitrogenous diets (35% of energy as protein and 5% as fat) based on either casein or soy protein isolate hydrolysate (SPI-H) for 4 wk. To measure exogenous carbohydrate and lipid oxidation, the mice were fed a diet containing (13)C-glucose or (13)C-triolein while they were in a respiratory chamber for 72 h. Postprandial energy expenditure was higher in the SPI-H than in the casein group; this difference was due to an increase in postprandial exogenous and endogenous carbohydrate oxidation. There were no differences in 24-h energy expenditure between dietary groups. Oxidation of exogenous carbohydrate tended to be higher (P = 0.054) in the SPI-H group during the 24 h of measurement. Fecal excretion of (13)C-glucose was lower but the excretion of lipid was higher in mice fed the SPI-H diet than in casein-fed mice. These results indicate that in type II diabetic mice, dietary SPI-H not only inhibits the absorption of dietary lipids and increases the absorption of dietary carbohydrates but also augments postprandial energy expenditure, which is accompanied by a postprandial increase in oxidation of dietary carbohydrates.


Subject(s)
Diabetes Mellitus, Type 2/metabolism , Dietary Carbohydrates/metabolism , Dietary Proteins/administration & dosage , Energy Metabolism , Soybean Proteins/administration & dosage , Animals , Body Weight , Carbon Isotopes/metabolism , Caseins/administration & dosage , Dietary Carbohydrates/pharmacokinetics , Dietary Fats/metabolism , Dietary Fats/pharmacokinetics , Energy Intake , Feces/chemistry , Intestinal Absorption , Male , Mice , Oxidation-Reduction , Triolein/administration & dosage , Triolein/metabolism , Triolein/pharmacokinetics
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