Patel M S, Raefsky C, Hu C W, Ho L
Biochem J. 1985 Mar 1;226(2):607-11. doi: 10.1042/bj2260607.
Chronic exposure of 3T3-L1 pre-adipocytes to dexamethasone plus 3-isobutyl-1-methylxanthine (IBMX) with or without insulin caused a significant increase in the specific activity of 'total' pyruvate dehydrogenase complex (PDC) and in the percentage of the 'active' form of the complex compared with cells exposed to a chronic insulin treatment or an acute treatment (2 days) with dexamethasone plus IBMX. In acute-drug-switch-over experiments, dexamethasone also caused an increase in the percentage of 'active' PDC in 3T3-L1 adipocytes. The results show that, in 3T3-L1 adipocytes, dexamethasone, even in the absence of insulin, increases the proportion of PDC in its 'active' form. The mechanism of the dexamethasone effect remains to be investigated.
将3T3-L1前脂肪细胞长期暴露于地塞米松加3-异丁基-1-甲基黄嘌呤(IBMX),无论有无胰岛素,与长期接受胰岛素处理或用地塞米松加IBMX进行急性处理(2天)的细胞相比,“总”丙酮酸脱氢酶复合体(PDC)的比活性以及该复合体“活性”形式的百分比均显著增加。在急性药物转换实验中,地塞米松也使3T3-L1脂肪细胞中“活性”PDC的百分比增加。结果表明,在3T3-L1脂肪细胞中,即使没有胰岛素,地塞米松也会增加处于“活性”形式的PDC的比例。地塞米松作用的机制仍有待研究。