Tissue-, substrate-, and site-specific characteristics of mitochondrial reactive oxygen species generation

• Published in: Free radical biology & medicine 2009-05, Vol.46 (9), p.1283-1297
• Main Authors: Tahara, Erich B., Navarete, Felipe D.T., Kowaltowski, Alicia J.
• Format: Article
• Language: English
• Subjects: Animals; Brain - metabolism; Electron Transport Chain Complex Proteins - antagonists & inhibitors; Electron Transport Chain Complex Proteins - physiology; Free radical; Hydrogen peroxide; Kidney - metabolism; Liver - metabolism; Male; Membrane Potential, Mitochondrial - drug effects; Membrane Transport Modulators - pharmacology; Mitochondria; Mitochondria - metabolism; Muscle, Skeletal - metabolism; Myocardium - metabolism; Organ Specificity; Oxidative Phosphorylation; Oxidative Stress; Oxygen Consumption; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; Respiration; Substrate Specificity; Superoxide radical
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2009.02.008

Reactive oxygen species are a by-product of mitochondrial oxidative phosphorylation, derived from a small quantity of superoxide radicals generated during electron transport. We conducted a comprehensive and quantitative study of oxygen consumption, inner membrane potentials, and H 2O 2 release in mitochondria isolated from rat brain, heart, kidney, liver, and skeletal muscle, using various respiratory substrates (α-ketoglutarate, glutamate, succinate, glycerol phosphate, and palmitoyl carnitine). The locations and properties of reactive oxygen species formation were determined using oxidative phosphorylation and the respiratory chain modulators oligomycin, rotenone, myxothiazol, and antimycin A and the uncoupler CCCP. We found that in mitochondria isolated from most tissues incubated under physiologically relevant conditions, reactive oxygen release accounts for 0.1–0.2% of O 2 consumed. Our findings support an important participation of flavoenzymes and complex III and a substantial role for reverse electron transport to complex I as reactive oxygen species sources. Our results also indicate that succinate is an important substrate for isolated mitochondrial reactive oxygen production in brain, heart, kidney, and skeletal muscle, whereas fatty acids generate significant quantities of oxidants in kidney and liver. Finally, we found that increasing respiratory rates is an effective way to prevent mitochondrial oxidant release under many, but not all, conditions. Altogether, our data uncover and quantify many tissue-, substrate-, and site-specific characteristics of mitochondrial ROS release.