Yourick J J, Beuving L J
J Recept Res. 1985;5(5-6):381-95. doi: 10.3109/10799898509041889.
Streptozotocin-induced diabetic rat liver was analyzed for glucocorticoid receptor (GR) content by saturation and Scatchard analysis. The hepatic GR content of streptozotocin-induced diabetic rats was significantly decreased from a control level of 0.17 +/- .01 pmol/mg protein to 0.11 +/- .01 pmol/mg protein. Insulin replacement therapy to the diabetic rat dramatically increased the hepatic GR content to 0.26 +/- 0.02 pmol/mg protein as compared to the diabetic value of 0.11 +/- 0.01 pmol/mg protein. A time course study of GR content in the diabetic rat liver demonstrated that after an initial decrease in hepatic GR content at 14 days, the 25-day diabetic receptor level elevated back to control levels. A significant increase in GR content over controls was observed in the 110-day diabetic rats. These results suggest that insulin has a role in the regulation of hepatic GR content.
通过饱和分析和Scatchard分析,对链脲佐菌素诱导的糖尿病大鼠肝脏中的糖皮质激素受体(GR)含量进行了分析。链脲佐菌素诱导的糖尿病大鼠肝脏GR含量从对照水平的0.17±0.01 pmol/mg蛋白质显著降低至0.11±0.01 pmol/mg蛋白质。与糖尿病大鼠0.11±0.01 pmol/mg蛋白质的数值相比,给糖尿病大鼠进行胰岛素替代治疗可使肝脏GR含量显著增加至0.26±0.02 pmol/mg蛋白质。对糖尿病大鼠肝脏GR含量的时间进程研究表明,在第14天肝脏GR含量最初下降后,25天糖尿病大鼠的受体水平回升至对照水平。在110天的糖尿病大鼠中观察到GR含量比对照组有显著增加。这些结果表明胰岛素在肝脏GR含量的调节中起作用。