4.2 Article

Abdominal Adipose Tissue: Early Metabolic Dysfunction Associated to Insulin Resistance and Oxidative Stress Induced by an Unbalanced Diet

期刊

HORMONE AND METABOLIC RESEARCH
卷 40, 期 11, 页码 794-800

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2008-1081502

关键词

abdominal adipose tissue metabolism; fructose-rich diet; fat tissue composition; fatty acid release; saturated and unsaturated fatty acids

资金

  1. National Fund for Scientific and Technological Research (FONCYT)
  2. National Research Council (CONICET)

向作者/读者索取更多资源

The possible contribution of early changes in lipid composition, function, and antioxidant status of abdominal adipose tissue (AAT) induced by a fructose-rich diet (FRD) to the development of insulin resistance (IR) and oxidative stress (OS) was studied. Wistar rats were fed with a commercial diet with (FRD) or without 10% fructose in the drinking water for 3 weeks. The glucose (G), triglyceride (TG), and insulin (1) plasma levels, and the activity of antioxidant enzymes, lyposoluble antioxidants, total glutathione (GSH), lipid peroxidation as TBARS, fatty acid (FA) composition of AAT-TG as well as their release by incubated pieces of AAT were measured. Rats fed with a FRD have significantly higher plasma levels of G, TG, and I. Their AAT showed a marked increase in content and ratios of saturated to monounsaturated and polyunsaturated FAs, TBARS, and catalase, GSH-transferase and GSH-reductase, together with a decrease in superoxide dismutase and GSH-peroxidase activity, and total GSH, alpha-tocopherol, beta-carotene and lycopene content. Incubated AAT from FRD released in vitro higher amount of free fatty acids (FFAs) with higher ratios of saturated to monounsaturated and polyunsaturated FAs. Our data suggest that FRD induced an early prooxidative state and metabolic dysfunction in AAT that would favor the overall development of IR and OS and further development of pancreatic beta-cell failure; therefore, its early control would represent an appropriate strategy to prevent alterations such as the development of type 2 diabetes.

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