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磺脲类药物通过GLUT4转运体转位刺激大鼠骨骼肌对葡萄糖的摄取。

Sulfonylureas stimulate glucose uptake through GLUT4 transporter translocation in rat skeletal muscle.

作者信息

Pulido N, Romero R, Suárez A I, Rodríguez E, Casanova B, Rovira A

机构信息

Department of Endocrinology, Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Spain.

出版信息

Biochem Biophys Res Commun. 1996 Nov 12;228(2):499-504. doi: 10.1006/bbrc.1996.1689.

Abstract

We studied the effect of gliclazide on glucose uptake and GLUT4 translocation in skeletal muscle. Rat hindquarters were perfused in the absence or presence of gliclazide (300 micrograms/ml), insulin or both drugs. The basal glucose uptake was increased 2.7-fold by gliclazide (p < 0.05). Gastrocnemius muscles perfused with gliclazide had a significant increase (2.4-fold) in the GLUT4 content in plasma membranes compared to basal conditions (p < 0.05). The stimulations produced by 1 nM insulin on muscle glucose uptake (2.8-fold) and on GLUT4 level in plasma membranes (2.5-fold) were similar to those produced by gliclazide. The effect of insulin on the glucose uptake and on the GLUT 4 translocation was significantly enhanced by gliclazide (3.4-fold and 3.7-fold vs basal, respectively). These data show that sulfonylureas stimulate glucose uptake in skeletal muscle by promoting the movement of GLUT4 to the plasma membrane.

摘要

我们研究了格列齐特对骨骼肌葡萄糖摄取及葡萄糖转运蛋白4(GLUT4)转位的影响。在不存在或存在格列齐特(300微克/毫升)、胰岛素或两种药物的情况下对大鼠后肢进行灌注。格列齐特使基础葡萄糖摄取增加了2.7倍(p<0.05)。与基础状态相比,灌注格列齐特的腓肠肌质膜中的GLUT4含量显著增加(2.4倍)(p<0.05)。1纳摩尔胰岛素对肌肉葡萄糖摄取(2.8倍)和质膜中GLUT4水平(2.5倍)的刺激作用与格列齐特产生的刺激作用相似。格列齐特显著增强了胰岛素对葡萄糖摄取及GLUT4转位的作用(分别相对于基础状态为3.4倍和3.7倍)。这些数据表明,磺脲类药物通过促进GLUT4向质膜的移动来刺激骨骼肌中的葡萄糖摄取。

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