Easom R A, Zammit V A
Biochem J. 1985 Sep 15;230(3):747-52. doi: 10.1042/bj2300747.
The expressed and total activities of HMG-CoA (3-hydroxy-3-methylglutaryl-CoA) reductase (EC 1.1.1.34) were measured in microsomal fractions prepared from cold-clamped liver samples [Easom & Zammit (1984) Biochem. J. 220, 733-738] from control or insulin-treated diabetic animals. Streptozotocin-induced diabetes resulted in a marked decrease in total activity of HMG-CoA reductase and in the fraction of the enzyme in the active form, but appreciable effects were only observed in the liver of animals in which the blood glucose was above 20 mM. Intravenous infusion of insulin into diabetic rats resulted in a rapid (less than 20 min) and total dephosphorylation of the enzyme in vivo without any change in total activity. Longer-term (4 h) treatment with insulin (injected intraperitoneally) produced a rapid increase in expressed/total HMG-CoA reductase activity ratio to about 90%, followed, after a lag of 2-3 h, by a 5-6-fold increase in total activity. These observations are discussed with respect to the possible role of insulin in generating and maintaining the respective diurnal rhythms in total and in expressed/total HMG-CoA reductase activity ratio observed for normal animals in vivo [Easom & Zammit (1984) Biochem. J. 220, 739-745].
从对照或胰岛素治疗的糖尿病动物的冷钳夹肝脏样本中制备微粒体组分,测定其中HMG-CoA(3-羟基-3-甲基戊二酰辅酶A)还原酶(EC 1.1.1.34)的表达活性和总活性[伊索姆和扎米特(1984年)《生物化学杂志》220卷,733 - 738页]。链脲佐菌素诱导的糖尿病导致HMG-CoA还原酶的总活性以及活性形式的酶比例显著降低,但仅在血糖高于20 mM的动物肝脏中观察到明显影响。给糖尿病大鼠静脉输注胰岛素导致该酶在体内迅速(少于20分钟)完全去磷酸化,而总活性没有任何变化。用胰岛素(腹腔注射)进行长期(4小时)治疗使表达的/总HMG-CoA还原酶活性比迅速增加至约90%,在延迟2 - 3小时后,总活性增加5 - 6倍。结合胰岛素在正常动物体内产生和维持HMG-CoA还原酶总活性以及表达的/总活性比的各自昼夜节律中可能发挥的作用,对这些观察结果进行了讨论[伊索姆和扎米特(1984年)《生物化学杂志》220卷,739 - 745页]。