May J M, de Haën C
J Biol Chem. 1979 Apr 10;254(7):2214-20.
Insulin stimulation of hydrogen peroxide production by rat epididymal fat cells was investigated by studying the oxidation of formate to CO2 by endogenous catalase. Under optimal concentrations of formate (0.1 to 1 mM) and glucose (0.275 mM), insulin stimulated formate oxidation 1.5- to 2.0-fold. Inhibitors of catalase activity, including nitrite and azide, inhibited both basal and insulin-stimulated formate oxidation at concentrations that did not interfere with insulin effects on glucose C-1 oxidation or glucose H-3 incorporation into lipids. The addition of exogenous catalase increased formate oxidation only slightly, while exogenous H2O2 (0.5 mM) stimulated formate oxidation by endogenous catalase strongly. These data indicate that the insulin-stimulated H2O2 production was intracellular. Insulin dose-response curves for formate oxidation were identical with those for glucose H-3 incorporation into lipids. The dependence of relative insulin effects on the logarithm of the glucose concentration was bell-shaped for formate oxidation and correlated highly with the coresponding dependences of glucose C-1 oxidation and glucose H-3 incorporation into lipids. This suggests that insulin stimulation of intracellular H2O2 production is linked to glucose metabolism. Since it is known that extracellular H2O2 can mimic insulin in several respects, these observations suggest that H2O2 may act as a "second messenger" for the observed effects of insulin.
通过研究内源性过氧化氢酶将甲酸氧化为二氧化碳,对胰岛素刺激大鼠附睾脂肪细胞产生过氧化氢的情况进行了研究。在甲酸(0.1至1 mM)和葡萄糖(0.275 mM)的最佳浓度下,胰岛素使甲酸氧化增加了1.5至2.0倍。过氧化氢酶活性抑制剂,包括亚硝酸盐和叠氮化物,在不干扰胰岛素对葡萄糖C-1氧化或葡萄糖H-3掺入脂质的作用的浓度下,抑制基础和胰岛素刺激的甲酸氧化。添加外源性过氧化氢酶仅略微增加甲酸氧化,而外源性H2O2(0.5 mM)强烈刺激内源性过氧化氢酶的甲酸氧化。这些数据表明胰岛素刺激产生的H2O2是细胞内的。甲酸氧化的胰岛素剂量反应曲线与葡萄糖H-3掺入脂质的曲线相同。相对胰岛素效应与葡萄糖浓度对数的关系对于甲酸氧化呈钟形,并且与葡萄糖C-1氧化和葡萄糖H-3掺入脂质的相应关系高度相关。这表明胰岛素刺激细胞内H2O2产生与葡萄糖代谢有关。由于已知细胞外H2O2在几个方面可以模拟胰岛素,这些观察结果表明H2O2可能作为胰岛素所观察到的效应的“第二信使”。