Dual effects of resveratrol on arterial damage induced by insulin resistance in aged mice

Aging leads to increased insulin resistance and arterial dysfunction, with oxidative stress playing an important role. This study explored the metabolic and arterial effects of a chronic treatment with resveratrol, an antioxidant polyphenol compound that has been shown to restore insulin sensitivity...

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Published in:The journals of gerontology. Series A, Biological sciences and medical sciences Vol. 69; no. 3; pp. 260 - 269
Main Authors: Baron, Stephanie, Bedarida, Tatiana, Cottart, Charles-Henry, Vibert, Francoise, Vessieres, Emilie, Ayer, Audrey, Henrion, Daniel, Hommeril, Baptiste, Paul, Jean-Louis, Renault, Gilles, Saubamea, Bruno, Beaudeux, Jean-Louis, Procaccio, Vincent, Nivet-Antoine, Valerie
Format: Journal Article
Language:English
Published: United States Oxford University Press 01-03-2014
Oxford University Press / The Gerontological Society of America
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Summary:Aging leads to increased insulin resistance and arterial dysfunction, with oxidative stress playing an important role. This study explored the metabolic and arterial effects of a chronic treatment with resveratrol, an antioxidant polyphenol compound that has been shown to restore insulin sensitivity and decrease oxidative stress, in old mice with or without a high-protein diet renutrition care. High-protein diet tended to increase insulin resistance and atheromatous risk. Resveratrol improved insulin sensitivity in old mice fed standard diet by decreasing homeostasis model of assessment-insulin resistance and resistin levels. However, resveratrol did not improve insulin resistance status in old mice receiving the high-protein diet. In contrast, resveratrol exhibited deleterious effects by increasing inflammation state and superoxide production and diminishing aortic distensibility. In conclusion, we demonstrate that resveratrol has beneficial or deleterious effects on insulin sensitivity and arterial function, depending on nutritional status in our models.
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ISSN:1079-5006
1758-535X
DOI:10.1093/gerona/glt081