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1.
Clin Nutr ; 27(2): 276-82, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18358572

ABSTRACT

BACKGROUND & AIMS: The aim of this experiment was to evaluate the potential beneficial effect of supplementation with different inulin-type fructan fractions against common features of the metabolic syndrome in a rat model of this syndrome (fructose-fed rat). METHODS: Forty Wistar rats were randomly divided into five groups and the animals received for 4 weeks either a semi-purified starch or fructose-based diet, or diets in which fructose was partially substituted with various fructans: 10 g/100 g of long-chain inulin or oligofructose, or an oligofructose-enriched inulin. After this period, blood pressure was measured and samples of blood and tissues were collected for selected biochemical analyses. RESULTS: As compared to the starch-fed group, the fructose-fed rats presented: hypertriglyceridemia, hypertension, increased susceptibility to heart peroxidation and renal damages. Long-chain inulin and oligofructose-enriched inulin supplementation prevented fructose induced elevated blood pressure, susceptibility to heart peroxidation and renal damages. All inulin-type fructans containing diets prevented fructose induced hypertriglyceridemia. CONCLUSIONS: These results suggest that supplementation with inulin-type fructans is efficient against fructose induced hypertension and that effects are most pronounced for long-chain inulin and oligofructose-enriched inulin. We hypothesize that the anti-hypertensive effect of inulin could be explained by the reduction of the high fructose induced oxidative stress.


Subject(s)
Fructans/pharmacology , Hypertension/prevention & control , Hypertriglyceridemia/prevention & control , Inulin/pharmacology , Oligosaccharides/pharmacology , Oxidative Stress/drug effects , Animals , Dietary Supplements , Disease Models, Animal , Fructans/chemistry , Fructose/administration & dosage , Fructose/adverse effects , Hypertension/blood , Hypertension/chemically induced , Hypertriglyceridemia/blood , Hypertriglyceridemia/chemically induced , Inulin/chemistry , Male , Oligosaccharides/chemistry , Random Allocation , Rats , Rats, Wistar , Starch
2.
Br J Nutr ; 96(5): 840-4, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17092371

ABSTRACT

Effects of different inulin-type fructan fractions were studied on atherosclerotic plaque formation in male apo E-deficient mice. Thirty-two mice were randomly divided into four groups and received either a semi-purified sucrose-based diet (control group), or diets in which sucrose was replaced in part by various inulin-type fructans (10 g/100 g): long-chain inulin, oligofructose, or an oligofructose-enriched inulin for 16 weeks. The presence of atherosclerotic plaques was assessed by histomorphometry in the aortic sinus. The apo E-deficient mice fed long-chain inulin or an oligofructose-enriched inulin had about 35 % and 25 % less atherosclerotic lesion area compared with the control group, respectively. Feeding long-chain inulin significantly reduced plasma cholesterol concentrations (P<0.001), and the three inulin-type fructans reduced triacylglycerol (TAG) concentrations compared with the control group (P<0.001). Both the long-chain inulin and an oligofructose-enriched inulin significantly lowered hepatic cholesterol concentrations compared with the control diet (P<0.05). Hepatic TAG concentrations were significantly lower in all three groups fed the fructan-supplemented diets v. the control group (P<0.0001). The results of the present study suggest that inhibition of atherosclerotic plaque formation is more potent in the presence of long-chain inulin, either alone or in combination with oligofructose (an oligofructose-enriched inulin), and that this probably is related to changes in lipid metabolism.


Subject(s)
Apolipoproteins E/deficiency , Atherosclerosis/drug therapy , Dietary Carbohydrates/administration & dosage , Inulin/administration & dosage , Animals , Atherosclerosis/pathology , Blood Pressure/drug effects , Body Weight/physiology , Cholesterol/blood , Dietary Sucrose/administration & dosage , Disease Models, Animal , Liver/chemistry , Male , Mice , Oligosaccharides/administration & dosage , Sinus of Valsalva/pathology , Triglycerides/blood
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