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For cellular fractionation, the tissues were homogenized in H-medium (70 mM sucrose, 220 mM mannitol, 2.5 mM HEPES, 2 mM EDTA, 0.1 mM phenylmethylsulfonylfluoride, pH 7.4) at 4°C and the fractions separated by differential centrifugation and the purity of the fractions were checked as described before ( Measurement of ROS production, NADPH oxidase (NOX) activity, and lipid and protein oxidation ROS production was measured in the liver and kidneys of exercised and sedentary control Wistar and type 2 diabetic GK rats using the DCFH-DA fluorescence method to measure the total peroxides as described before ( Measurement of GSH level, and GSH-peroxidase, GSH reductase, and SOD activities The enzymatic and non-enzymatic physiological antioxidants play an important role in oxidative stress defense