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二甲双胍可诱导来自不同脂肪部位的人前体脂肪细胞分化成的脂肪细胞摄取葡萄糖。

Metformin induces glucose uptake in human preadipocyte-derived adipocytes from various fat depots.

机构信息

Department of Biomedicine, University Hospital Basel, CH-4031 Basel, Switzerland.

出版信息

Diabetes Obes Metab. 2010 Apr;12(4):356-9. doi: 10.1111/j.1463-1326.2009.01169.x.

Abstract

To evaluate the effect of metformin on basal and insulin-induced glucose uptake in subcutaneous and visceral preadipocyte-derived adipocytes from obese and non-obese patients, preadipocytes were obtained from subcutaneous and visceral fat depots during abdominal surgery. Differentiation efficiency was evaluated by measurement of intracellular triglyceride accumulation. Preadipocyte-derived adipocytes were treated with metformin (1 mM) for 24 h with or without the addition of insulin (100 nM) for 20 min and glucose uptake was measured. In cells from each donor, intracellular triglyceride accumulation was more abundant in subcutaneous preadipocyte-derived adipocytes than in visceral preadipocyte-derived adipocytes (p < 0.001). Insulin stimulated glucose uptake in subcutaneous preadipocyte-derived adipocytes from both non-obese and obese patients (p < 0.001 vs. basal). In visceral preadipocyte-derived adipocytes, insulin did not increase basal glucose uptake. In subcutaneous preadipocyte-derived adipocytes from non-obese and obese patients, metformin alone increased glucose uptake to 2.7 +/- 0.2 (p < 0.001) and 2.1 +/- 0.1 fold (p < 0.001) respectively. Metformin increased glucose uptake in visceral preadipocyte-derived adipocytes from non-obese (1.7 +/- 0.1 fold vs. basal, p < 0.001) and obese (2.0 +/- 0.2 fold vs. basal, p < 0.001) patients. Combined treatment with metformin and insulin increased glucose uptake in subcutaneous preadipocyte-derived adipocytes from both non-obese and obese patients (p < 0.001 vs. insulin alone). In preadipocyte-derived adipocytes glucose uptake is induced by metformin independent of the fat depot origin of the preadipocytes (subcutaneous or visceral) and the obesity state of the patients (non-obese or obese). In adipocytes, metformin seems to induce glucose uptake independent of insulin suggesting an alternative mechanism of action of this drug.

摘要

为了评估二甲双胍对肥胖和非肥胖患者皮下和内脏前体脂肪衍生脂肪细胞基础和胰岛素诱导的葡萄糖摄取的影响,在腹部手术期间从皮下和内脏脂肪组织中获得前体脂肪细胞。通过测量细胞内甘油三酯积累来评估分化效率。用二甲双胍(1mM)处理前体脂肪衍生的脂肪细胞 24 小时,有或没有添加胰岛素(100nM)20 分钟,并测量葡萄糖摄取。在每个供体的细胞中,皮下前体脂肪衍生的脂肪细胞中的细胞内甘油三酯积累比内脏前体脂肪衍生的脂肪细胞更丰富(p<0.001)。胰岛素刺激非肥胖和肥胖患者的皮下前体脂肪衍生的脂肪细胞中的葡萄糖摄取(与基础相比,p<0.001)。在内脏前体脂肪衍生的脂肪细胞中,胰岛素不会增加基础葡萄糖摄取。在非肥胖和肥胖患者的皮下前体脂肪衍生的脂肪细胞中,二甲双胍单独使葡萄糖摄取增加 2.7+/-0.2(p<0.001)和 2.1+/-0.1 倍(p<0.001)。二甲双胍增加非肥胖(1.7+/-0.1 倍与基础相比,p<0.001)和肥胖(2.0+/-0.2 倍与基础相比,p<0.001)患者的内脏前体脂肪衍生的脂肪细胞中的葡萄糖摄取。二甲双胍和胰岛素联合治疗增加了非肥胖和肥胖患者的皮下前体脂肪衍生的脂肪细胞中的葡萄糖摄取(与胰岛素单独治疗相比,p<0.001)。在脂肪细胞中,二甲双胍诱导的葡萄糖摄取独立于前体脂肪细胞(皮下或内脏)的脂肪库起源和患者的肥胖状态(非肥胖或肥胖)。在脂肪细胞中,二甲双胍似乎独立于胰岛素诱导葡萄糖摄取,提示该药物的替代作用机制。

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