4.7 Article

Effects of a grapeseed procyanidin extract (GSPE) on insulin resistance

期刊

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
卷 21, 期 10, 页码 961-967

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2009.08.001

关键词

High-fat diet; Adipose tissue; Obesity; Procyanidins; Insulin resistance

资金

  1. Ministerio de Ciencia e Innovacion (MICINN) of the Spanish Government [AGL2008-01310/ALI, AGL2008-00387/ALI]
  2. Rovira i Virgili University in Tarragona

向作者/读者索取更多资源

Flavonoids are beneficial compounds against risk factors for metabolic syndrome, but their effects and the mechanisms on glucose homeostasis modulation are not well defined. In the present study, we first checked the efficacy of grapeseed procyanidin extract (GSPE) for stimulating glucose uptake in insulin-resistant 3T3-L1 adipocytes. Results show that when resistance is induced with chronic insulin treatment, GSPE maintain a higher stimulating capacity than insulin. In contrast, when dexamethasone is used as the resistance-inducing agent, GSPE is less effective. Next we evaluated how effective different GSPE treatments are at improving glucose metabolism in hyperinsulinemic animals (fed a cafeteria diet). GSPE reduced plasma insulin levels. The lower dose (25 mg GSPE/kg body weight per day) administered for 30 days improved the HOmeostasis Model Assessment-insulin resistance index. This was accompanied by down-regulation of Pparg2, Glut4 and Irs1 in mesenteric white adipose tissue. Similarly, a chronic GSPE treatment of insulin-resistant 3T3-L1 adipocytes down-regulated the mRNA levels of those adipocyte markers, although cells were still able to respond to the acute stimulation of glucose uptake. In summary, 25 mg/kg body weight per day of GSPE has a positive long-term effect on glucose homeostasis, and GSPE could be targeted at adipose tissue, where it might directly stimulate glucose uptake. This work also highlights the need to carefully consider the bioactive dose, since a higher dose does not necessarily correlate to a greater positive effect. (C) 2010 Elsevier Inc. All rights reserved.

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