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葡萄籽原花青素提取物(GSPE)对胰岛素抵抗的影响。

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

机构信息

Department of Biochemistry and Biotechnology, Rovira i Virgili University, Tarragona, 43007 Spain.

出版信息

J Nutr Biochem. 2010 Oct;21(10):961-7. doi: 10.1016/j.jnutbio.2009.08.001. Epub 2009 Dec 4.

DOI:10.1016/j.jnutbio.2009.08.001
PMID:19962298
Abstract

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.

摘要

类黄酮是对抗代谢综合征危险因素的有益化合物,但它们对葡萄糖稳态调节的作用和机制尚不清楚。在本研究中,我们首先检查了葡萄籽原花青素提取物(GSPE)对胰岛素抵抗的 3T3-L1 脂肪细胞中葡萄糖摄取的刺激作用。结果表明,当用慢性胰岛素处理诱导抵抗时,GSPE 保持比胰岛素更高的刺激能力。相比之下,当使用地塞米松作为诱导抵抗的试剂时,GSPE 的效果较差。接下来,我们评估了不同 GSPE 处理在改善高胰岛素血症动物(喂食自助餐厅饮食)葡萄糖代谢中的有效性。GSPE 降低了血浆胰岛素水平。低剂量(25mgGSPE/kg 体重/天)给药 30 天可改善稳态模型评估-胰岛素抵抗指数。这伴随着肠白色脂肪组织中 Pparg2、Glut4 和 Irs1 的下调。同样,慢性 GSPE 处理胰岛素抵抗的 3T3-L1 脂肪细胞也下调了这些脂肪细胞标志物的 mRNA 水平,尽管细胞仍然能够对葡萄糖摄取的急性刺激做出反应。总之,每天 25mg/kg 体重的 GSPE 对葡萄糖稳态具有积极的长期影响,GSPE 可能靶向脂肪组织,在脂肪组织中它可能直接刺激葡萄糖摄取。这项工作还强调需要仔细考虑生物活性剂量,因为高剂量不一定与更大的积极效果相关。

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