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黄酮类化合物对脂肪细胞基础状态和胰岛素刺激的 2-脱氧葡萄糖摄取的影响。

Effect of flavonoids on basal and insulin-stimulated 2-deoxyglucose uptake in adipocytes.

机构信息

Else-Kröner-Fresenius Center for Nutritional Medicine, Technische Universität München, Freising, Germany.

出版信息

Mol Nutr Food Res. 2011 May;55 Suppl 1:S26-34. doi: 10.1002/mnfr.201000372. Epub 2011 Jan 31.

Abstract

SCOPE

The adipose tissue is a major site of insulin action and contributes substantially to energy homeostasis. Insulin increases the extraction of glucose from circulation into adipose tissue by recruiting the glucose transporter GLUT4 to the plasma membrane. It has been proposed that dietary flavonoids may interfere with glucose transport processes.

METHODS AND RESULTS

We have used murine 3T3-L1 adipocytes and isolated mature human adipocytes to assess the interaction of selected flavonoids with glucose uptake, both in the basal state and after insulin stimulation. Kinetic characterization of 2-deoxyglucose uptake in the basal state revealed in both cell types an apparent K(m) of around 8 mM with no change in affinity but a significant increase in maximal influx in the presence of insulin. A screening of representative flavonoids of different structural classes revealed the flavanone naringenin and the isoflavone daidzein to affect glucose transport significantly with half-maximal inhibition at concentrations of around 60-80 μM for basal and 70-110 μM for insulin-stimulated glucose uptake in both 3T3-L1 adipocytes and mature human adipocytes.

CONCLUSION

Considering attainable plasma concentrations of flavonoids in vivo, we assume that even under physiological conditions naringenin and daidzein could impair glucose removal from plasma, which may pose a risk to patients with diabetes mellitus.

摘要

范围

脂肪组织是胰岛素作用的主要部位,对能量稳态有重要贡献。胰岛素通过将葡萄糖转运蛋白 GLUT4 募集到质膜来增加葡萄糖从循环中向脂肪组织的提取。有人提出,膳食类黄酮可能会干扰葡萄糖转运过程。

方法和结果

我们使用鼠 3T3-L1 脂肪细胞和分离的成熟人脂肪细胞来评估选定的类黄酮与葡萄糖摄取的相互作用,包括在基础状态和胰岛素刺激后。在基础状态下 2-脱氧葡萄糖摄取的动力学特征表明,在两种细胞类型中,表观 K(m) 约为 8mM,亲和力没有变化,但胰岛素存在时最大内流显著增加。对不同结构类别的代表性类黄酮的筛选显示,黄烷酮柚皮素和异黄酮大豆苷元显著影响葡萄糖转运,在 3T3-L1 脂肪细胞和成熟人脂肪细胞中,基础葡萄糖摄取的半最大抑制浓度约为 60-80μM,胰岛素刺激的葡萄糖摄取的半最大抑制浓度约为 70-110μM。

结论

考虑到体内类黄酮的可达到血浆浓度,我们假设即使在生理条件下,柚皮素和大豆苷元也可能会损害从血浆中去除葡萄糖,这可能会对糖尿病患者构成风险。

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