Kurtz J W, Wells W W
J Biol Chem. 1981 Nov 10;256(21):10870-5.
To determine the relative contributions of glucose, insulin, dexamethasone, and triiodothyronine to the induction of hepatic glucose-6-phosphate dehydrogenase, hepatocytes isolated from normal or adrenalectomized rats, either fasted or fed, were examined in culture. Addition of insulin (42 milliunits/ml, 0.9 microM) and dexamethasone (1 microM) to hepatocytes obtained from 3-day-fasted rats and cultured for 48 h in serum-free Dulbecco's medium resulted in a 7- to 11-fold increase in Glc-6-P dehydrogenase specific activity compared with a 2- to 3-fold increase in activity in control cultures incubated without added hormones. The effects of insulin and dexamethasone were independent of DNA synthesis, dose-dependent, and additive; each contributing about one-half of the total response. Medium glucose was neither sufficient nor necessary for the insulin- or dexamethasone-stimulated increase in Glc-6-P dehydrogenase specific activity. Addition of triiodothyronine (10 microM) preferentially blocked the dexamethasone-stimulated increase in Glc-6-P dehydrogenase specific activity. Insulin failed to stimulate the induction of Glc-6-P dehydrogenase in hepatocytes obtained from normal fed rats or from fasted and fed adrenalectomized rats. However, insulin caused a significant increase in the Glc-6-P dehydrogenase specific activity of these cells when dexamethasone was concurrently added to the culture medium.
为了确定葡萄糖、胰岛素、地塞米松和三碘甲状腺原氨酸对肝葡萄糖-6-磷酸脱氢酶诱导的相对贡献,我们在培养中检测了从正常或肾上腺切除的大鼠中分离的肝细胞,这些大鼠分别处于禁食或进食状态。向从禁食3天的大鼠获得的肝细胞中添加胰岛素(42毫单位/毫升,0.9微摩尔)和地塞米松(1微摩尔),并在无血清的杜尔贝科培养基中培养48小时,与未添加激素的对照培养物中活性增加2至3倍相比,葡萄糖-6-磷酸脱氢酶的比活性增加了7至11倍。胰岛素和地塞米松的作用与DNA合成无关,呈剂量依赖性且具有加和性;各自约占总反应的一半。培养基中的葡萄糖对于胰岛素或地塞米松刺激的葡萄糖-6-磷酸脱氢酶比活性增加既非充分条件也非必要条件。添加三碘甲状腺原氨酸(10微摩尔)优先阻断了地塞米松刺激的葡萄糖-6-磷酸脱氢酶比活性增加。胰岛素未能刺激从正常进食大鼠或禁食和进食的肾上腺切除大鼠获得的肝细胞中葡萄糖-6-磷酸脱氢酶的诱导。然而,当将地塞米松同时添加到培养基中时,胰岛素导致这些细胞的葡萄糖-6-磷酸脱氢酶比活性显著增加。