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首页> 外文期刊>The biochemical journal >Changes in uncoupling protein and GLUT4 glucose transporter expressions in interscapular brown adipose tissue of diabetic rats: relative roles of hyperglycaemia and hypoinsulinaemia
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Changes in uncoupling protein and GLUT4 glucose transporter expressions in interscapular brown adipose tissue of diabetic rats: relative roles of hyperglycaemia and hypoinsulinaemia

机译:糖尿病大鼠肩ular棕色脂肪组织中解偶联蛋白和GLUT4葡萄糖转运蛋白表达的变化:高血糖和低胰岛素血症的相对作用

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pWe have studied the time course and relative effects of hypoinsulinaemia and hyperglycaemia on concentrations of uncoupling protein (UCP) and glucose transporter (GLUT4) and their mRNAs in brown adipose tissue (BAT) during the early phase of diabetes induced by streptozotocin. Two days after intravenous injection of streptozotocin, plasma insulin concentration was at its lowest and glycaemia was higher than 22 mmol/l. After 3 days, a 60% decrease in BAT UCP mRNA concentration and a 36% decrease in UCP was observed. Concomitantly, there was an 80% decrease in GLUT4 mRNA and a 44% decrease in GLUT4 levels. When hyperglycaemia was prevented by infusing phlorizin into diabetic rats, BAT UCP mRNA and protein levels were further decreased (respectively 90% and 60% lower than in control rats). In contrast, the marked decreases in GLUT4 mRNA and protein concentrations in BAT were similar in hyperglycaemic and normoglycaemic diabetic rats. Infusion of physiological amounts of insulin restored normoglycaemia in diabetic rats, and BAT UCP and GLUT4 mRNA and protein concentrations were maintained at the level of control rats. When insulin infusion was stopped, a 75% decrease in BAT UCP mRNA level and a 75% decrease in GLUT4 mRNA level were observed after 24 h, but UCP and GLUT4 concentrations did not decrease. This study shows that insulin plays an important role in the regulation of UCP and GLUT4 mRNA and protein concentrations in BAT. Hyperglycaemia partially prevents the rapid decrease in concentration of UCP and its mRNA observed in insulinopenic diabetes whereas it did not affect the decrease in GLUT4 mRNA and protein concentration. It is suggested that UCP is produced by a glucose-dependent gene./p
机译:>我们研究了链脲佐菌素诱导的糖尿病早期阶段低胰岛素血症和高血糖症对棕色脂肪组织(BAT)中解偶联蛋白(UCP)和葡萄糖转运蛋白(GLUT4)的表达及其时间的影响及其相对影响。静脉注射链脲佐菌素两天后,血浆胰岛素浓度最低,血糖高于22 mmol / l。 3天后,观察到BAT UCP mRNA浓度降低了60%,UCP降低了36%。同时,GLUT4 mRNA降低了80%,GLUT4水平降低了44%。当通过向糖尿病大鼠中注射氟硝嗪来预防高血糖症时,BAT UCP mRNA和蛋白水平进一步降低(分别比对照组大鼠低90%和60%)。相反,高血糖和高血糖糖尿病大鼠中BAT中GLUT4 mRNA和蛋白浓度的显着下降相似。在糖尿病大鼠中,注入生理量的胰岛素可恢复正常血糖,BAT UCP和GLUT4 mRNA和蛋白浓度保持在对照组大鼠水平。停止胰岛素输注后,在24小时后观察到BAT UCP mRNA水平降低了75%,GLUT4 mRNA水平降低了75%,但UCP和GLUT4浓度并未降低。这项研究表明,胰岛素在BAT中UCP和GLUT4 mRNA和蛋白质浓度的调节中起着重要作用。高血糖症部分阻止了在胰岛素缺乏性糖尿病中观察到的UCP及其mRNA的浓度迅速降低,而并未影响GLUT4 mRNA和蛋白浓度的降低。提示UCP是由葡萄糖依赖性基因产生的。

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