南方医科大学学报 ›› 2014, Vol. 34 ›› Issue (07): 1061-.

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慢性间歇性缺氧对大鼠骨骼肌葡萄糖转运蛋白4表达的影响

谭健,莫海兰,李洁,吴应玲,何晓丽,李兵   

  • 出版日期:2014-07-20 发布日期:2014-07-20

Effects of chronic intermittent hypoxia on glucose transporter 4 expression in rat skeletal
muscles

  • Online:2014-07-20 Published:2014-07-20

摘要: 目的探讨慢性间歇性缺氧所致炎症因子以及复氧对大鼠糖代谢及骨骼肌葡萄糖转运蛋白4(GLUT-4)表达的影响。方
法24只SD雄性大鼠,分为空白组(UC组)、慢性间歇性缺氧组(CIH组)和复氧组(RH组);所有大鼠在模型建立后,分别用氧化
酶-过氧化物酶法、放射免疫法、ELISA检测血糖、血清胰岛素及炎症因子的变化;Western blotting检测骨骼肌GLUT-4蛋白的表
达。结果大鼠空腹血糖,CIH组高于UC组和RH组(P<0.05),RH组高于UC组(P<0.05);血清胰岛素及胰岛素抵抗指数,CIH
组高于UC组和RH组(P<0.05)。各组大鼠血清炎症指标TNF-α、IL-6,CIH组显著高于UC组和RH组(P<0.05),RH组高于UC
组(P<0.05)。大鼠骨骼肌GLUT4蛋白,CIH组显著低于UC组和RH组(P<0.05),RH组低于UC组(P<0.05)。结论慢性间歇
性缺氧可引起大鼠体内炎症因子增加及胰岛素抵抗;大鼠胰岛素抵抗与炎症因子所致的骨骼肌GLUT-4蛋白量降低有关。

Abstract: Objective To study the effect of chronic intermittent hypoxia-induced inflammatory cytokines and reoxygenation on
glucose transporter 4 (GLUT-4) expression in rat skeletal muscles. Methods Twenty-four male Sprague-Dawley rats were
randomly assigned to blank control group, chronic intermittent hypoxia (CIH) group, and reoxygenation group. At the end of
the experiment, fasting blood glucose (FBG), fasting blood insulin (FINS) and serum inflammatory cytokine levels were
measured with glucose oxidase-peroxidase, insulin radioimmunoassay and ELISA, respectively. Homeostasis model
assessment (IRI) was used to evaluate insulin resistance in the rats, and GLUT-4 protein expression in the skeletal muscles was
measured with Western blotting. Results Compared with the blank control group, CIH resulted in significantly increased
fasting blood glucose, blood insulin levels and insulin resistance index (IRI) (P<0.05); fasting blood glucose was significantly
elevated in reoxygenation group (P<0.05). Inflammatory cytokines levels (IL-6 and TNF-α) were significantly higher in CIH
group than in the blank control and reoxygenation groups (P<0.05), and were higher in reoxygenation group than in the blank
control group. GLUT-4 expression in the skeletal muscles was significantly reduced after CIH (P<0.05) but increased after
subsequent reoxygenation (P<0.05). Conclusions CIH can cause increased release of inflammatory cytokines to lower GLUT-4
protein expression in the skeletal muscles, which contributes to insulin resistance in adult rats.