Slieker L J, Sundell K L, Heath W F, Osborne H E, Bue J, Manetta J, Sportsman J R
Diabetes Research Division, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285.
Diabetes. 1992 Feb;41(2):187-93. doi: 10.2337/diab.41.2.187.
We used antibodies to the fat/muscle glucose transporter (GLUT4) and the liver glucose transporter (GLUT2) to measure levels of these proteins in various tissues of two rodent models of non-insulin-dependent (type II) diabetes mellitus: the obese spontaneously diabetic male Zucker fa/fa rat (ZDF/drt) and the male viable yellow Avy/a obese diabetic mouse. The ZDF/drt strain generally develops overt diabetes associated with decreased plasma insulin levels. Depending on the age of the animals, the ZDF/drt rats can be arbitrarily segregated into age-matched obese, mildly diabetic (blood glucose less than 11 mM) and obese, and severely diabetic (blood glucose greater than 20 mM) groups. Avy/a mice are comparably hyperglycemic but unlike the ZDF/drt rats are severely hyperinsulinemic. In both groups of diabetic animals, GLUT4 in adipose tissue, heart, and skeletal muscle was reduced 25-55%, and GLUT2 in liver was increased 30-40%, relative to lean, age-matched controls. However, when the mildly diabetic ZDF/drt rats were compared to the lean controls, the only significant difference was a 25% reduction of GLUT4 in heart. Within all of the ZDF/drt rats (excluding the lean controls), GLUT2 in liver and GLUT4 in adipose tissue, heart, and skeletal muscle correlated significantly with glycemia. These data suggest that, in these two models of type II diabetes, glucose transporter levels in muscle, adipose tissue, and liver are regulated in a tissue-selective manner in response to changes in insulin and glucose. Furthermore, at least in the ZDF/drt rat, alterations in GLUT2 and/or GLUT4 protein levels appear not to be associated with obesity per se but appear to be secondary to the severely diabetic state.(ABSTRACT TRUNCATED AT 250 WORDS)
我们使用针对脂肪/肌肉葡萄糖转运蛋白(GLUT4)和肝脏葡萄糖转运蛋白(GLUT2)的抗体,来测量两种非胰岛素依赖型(II型)糖尿病啮齿动物模型各组织中这些蛋白质的水平:肥胖自发糖尿病雄性 Zucker fa/fa 大鼠(ZDF/drt)和雄性存活黄色Avy/a肥胖糖尿病小鼠。ZDF/drt品系通常会发展为明显的糖尿病,并伴有血浆胰岛素水平降低。根据动物的年龄,ZDF/drt大鼠可被任意分为年龄匹配的肥胖、轻度糖尿病(血糖低于11 mM)和肥胖、重度糖尿病(血糖高于20 mM)组。Avy/a小鼠同样血糖过高,但与ZDF/drt大鼠不同的是,它们严重高胰岛素血症。在两组糖尿病动物中,相对于年龄匹配的瘦对照,脂肪组织、心脏和骨骼肌中的GLUT4减少了25 - 55%,肝脏中的GLUT2增加了30 - 40%。然而,当将轻度糖尿病的ZDF/drt大鼠与瘦对照进行比较时,唯一显著的差异是心脏中GLUT4减少了25%。在所有ZDF/drt大鼠(不包括瘦对照)中,肝脏中的GLUT2以及脂肪组织、心脏和骨骼肌中的GLUT4与血糖显著相关。这些数据表明,在这两种II型糖尿病模型中,肌肉、脂肪组织和肝脏中的葡萄糖转运蛋白水平会根据胰岛素和葡萄糖的变化以组织选择性方式进行调节。此外,至少在ZDF/drt大鼠中,GLUT2和/或GLUT4蛋白水平的改变似乎并非与肥胖本身相关,而是继发于严重的糖尿病状态。(摘要截取自250字)