Prolonged Exposure to Insulin Induces Mitochondrion-Derived Oxidative Stress through Increasing Mitochondrial Cholesterol Content in Hepatocytes

• DOI: 10.1210/en.2011-2119
• Publication Date: 2012-02-29T05:35:04Z
• Authors: Shuang Mei; Haihua Gu; Xuefeng Yang; Huailan Guo; Zhenqi Liu; Wenhong Cao
• Keywords: Male; Membrane Potential, Mitochondrial; 0301 basic medicine; Insulin Glargine; Cell Line; Mitochondria; Insulin, Long-Acting; Mice; Oxidative Stress; 03 medical and health sciences; Cholesterol; Hepatocytes; Animals; Hypoglycemic Agents; Insulin; Reactive Oxygen Species

We addressed the link between excessive exposure to insulin and mitochondrion-derived oxidative stress in this study and found that prolonged exposure to insulin increased mitochondrial cholesterol in cultured hepatocytes and in mice and stimulated production of reactive oxygen species (ROS) and decreased the reduced glutathione to glutathione disulfide ratio in cultured hepatocytes. Exposure of isolated hepatic mitochondria to cholesterol alone promoted ROS emission. The oxidative stress induced by the prolonged exposure to insulin was prevented by inhibition of cholesterol synthesis with simvastatin. We further found that prolonged exposure to insulin decreased mitochondrial membrane potential and the increased ROS production came from mitochondrial respiration complex I. Finally, we observed that prolonged exposure to insulin decreased mitochondrial membrane fluidity in a cholesterol synthesis-dependent manner. Together our results demonstrate that excess exposure to insulin causes mitochondrion-derived oxidative stress through cholesterol synthesis in hepatocytes.