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二甲双胍可增加胰岛素抵抗的人体骨骼肌中胰岛素刺激的葡萄糖转运。

Metformin increases insulin-stimulated glucose transport in insulin-resistant human skeletal muscle.

作者信息

Galuska D, Zierath J, Thörne A, Sonnenfeld T, Wallberg-Henriksson H

机构信息

Department of Clinical Physiology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Diabete Metab. 1991 May;17(1 Pt 2):159-63.

PMID:1936469
Abstract

The effect of metformin (0.1 mM) on glucose transport was investigated in healthy control and in insulin-resistant human skeletal muscle. Muscle samples (200-400 mg) were obtained from the rectus abdominis muscle (abdominal surgery) or from the vastus lateralis portion of the quadriceps femoris muscle (open biopsy technique) from 8 healthy controls (age 38 +/- 4 yrs, BMI 23 +/- 1) and from 6 insulin-resistant subjects (age 53 +/- 5 yrs, BMI 30 +/- 2). Metformin had no effect on basal or insulin-stimulated (100 microU/ml) 3-0-methylglucose transport in incubated muscle strips from healthy subjects. Muscle tissue from the insulin resistant group did not respond to 100 microU/ml of insulin (0.73 +/- 0.17 for basal and 0.81 +/- 0.22 mumol x ml-1 x h-1 for insulin-stimulation, NS). Basal glucose transport was unaffected by metformin, whereas insulin-stimulated (100 microU/ml) glucose transport was increased by 63% in the insulin-resistant muscles (0.73 +/- 0.17 in the absence vs 1.19 +/- 0.18 mumol x ml-1 x h-1 in the presence of metformin, p less than 0.05). In conclusion, metformin abolishes insulin-resistance in human skeletal muscle by normalizing insulin-stimulated glucose transport accross the muscle cell membrane. The mechanism for this effect remains to be elucidated.

摘要

在健康对照者和胰岛素抵抗的人体骨骼肌中研究了二甲双胍(0.1 mM)对葡萄糖转运的影响。从8名健康对照者(年龄38±4岁,体重指数23±1)的腹直肌(腹部手术)或股四头肌的外侧肌部分(开放活检技术)以及6名胰岛素抵抗受试者(年龄53±5岁,体重指数30±2)获取肌肉样本(200 - 400 mg)。二甲双胍对健康受试者孵育的肌条中基础或胰岛素刺激(100微单位/毫升)的3 - O - 甲基葡萄糖转运没有影响。胰岛素抵抗组的肌肉组织对100微单位/毫升胰岛素无反应(基础状态下为0.73±0.17,胰岛素刺激下为0.81±0.22微摩尔·毫升⁻¹·小时⁻¹,无显著性差异)。基础葡萄糖转运不受二甲双胍影响,而在胰岛素抵抗的肌肉中,胰岛素刺激(100微单位/毫升)的葡萄糖转运增加了63%(无二甲双胍时为0.73±0.17,有二甲双胍时为1.19±0.18微摩尔·毫升⁻¹·小时⁻¹,p<0.05)。总之,二甲双胍通过使胰岛素刺激的跨肌细胞膜葡萄糖转运正常化,消除了人体骨骼肌中的胰岛素抵抗。这种作用的机制仍有待阐明。

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