Metabolic Syndrome and Hypertension Resulting from Fructose Enriched Diet in Wistar Rats

Author:

Dupas Julie1,Feray Annie12,Goanvec Christelle13ORCID,Guernec Anthony12,Samson Nolwenn4,Bougaran Pauline1,Guerrero François12ORCID,Mansourati Jacques15ORCID

Affiliation:

1. EA 4324-Optimisation des Régulations Physiologiques, Institut Brestois Santé Agro Matières, Université de Bretagne Occidentale, 6 avenue Victor Le Gorgeu, 29238 Brest Cedex 3, France

2. UFR Sciences du Sport et de l’Education, 20 avenue Victor Le Gorgeu, 29238 Brest Cedex 3, France

3. UFR Sciences et Techniques, 6 avenue Victor Le Gorgeu, 29238 Brest Cedex 3, France

4. Institut Universitaire de Cardiologie et de Pneumologie de Québec, Université de Laval, 2725 chemin Ste-Foy, Québec, QC, Canada G1V 4G5

5. Département de Cardiologie, Centre Hospitalo-Universitaire de Brest, boulevard Tanguy Prigent, 29200 Brest, France

Abstract

Increased sugar consumption, especially fructose, is strongly related to the development of type 2 diabetes (T2D) and metabolic syndrome. The aim of this study was to evaluate long term effects of fructose supplementation on Wistar rats. Three-week-old male rats were randomly divided into 2 groups: control (C;n=14) and fructose fed (FF;n=18), with a fructose enriched drink (20–25% w/v fructose in water) for 21 weeks. Systolic blood pressure, fasting glycemia, and bodyweight were regularly measured. Glucose tolerance was evaluated three times using an oral glucose tolerance test. Insulin levels were measured concomitantly and insulin resistance markers were evaluated (HOMA 2-IR, Insulin Sensitivity Index for glycemia (ISI-gly)). Lipids profile was evaluated on plasma. This fructose supplementation resulted in the early induction of hypertension without renal failure (stable theoretical creatinine clearance) and in the progressive development of fasting hyperglycemia and insulin resistance (higher HOMA 2-IR, lower ISI-gly) without modification of glucose tolerance. FF rats presented dyslipidemia (higher plasma triglycerides) and early sign of liver malfunction (higher liver weight). Although abdominal fat weight was increased in FF rats, no significant overweight was found. In Wistar rats, 21 weeks of fructose supplementation induced a metabolic syndrome (hypertension, insulin resistance, and dyslipidemia) but not T2D.

Funder

Fédération Française de Cardiologie

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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