Assessing bioenergetic function in response to oxidative stress by metabolic profiling |
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Authors: | Dranka Brian P Benavides Gloria A Diers Anne R Giordano Samantha Zelickson Blake R Reily Colin Zou Luyun Chatham John C Hill Bradford G Zhang Jianhua Landar Aimee Darley-Usmar Victor M |
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Affiliation: | a Department of Pathology and Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USAb Department of Cardiovascular Medicine, University of Louisville, Louisville, KY 40202, USA |
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Abstract: | It is now clear that mitochondria are an important target for oxidative stress in a broad range of pathologies, including cardiovascular disease, diabetes, neurodegeneration, and cancer. Methods for assessing the impact of reactive species on isolated mitochondria are well established but constrained by the need for large amounts of material to prepare intact mitochondria for polarographic measurements. With the availability of high-resolution polarography and fluorescence techniques for the measurement of oxygen concentration in solution, measurements of mitochondrial function in intact cells can be made. Recently, the development of extracellular flux methods to monitor changes in oxygen concentration and pH in cultures of adherent cells in multiple-sample wells simultaneously has greatly enhanced the ability to measure bioenergetic function in response to oxidative stress. Here we describe these methods in detail using representative cell types from renal, cardiovascular, nervous, and tumorigenic model systems while illustrating the application of three protocols to analyze the bioenergetic response of cells to oxidative stress. |
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Keywords: | 15d-PGJ2, 15-deoxy-Δ12,14-prostaglandin J2 2-DG, 2-deoxy-d-glucose AUC, area under the curve Deta NO, Deta NONOate, (Z)-1-[2-(2-aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate DMNQ, 2,3-dimethoxy-1,4-napthoquinone DPI, diphenyleneiodonium ECAR, extracellular acidification rate FCCP, carbonyl cyanide p-(trifluoromethoxy)phenylhydrazone GAPDH, glyceraldehyde-3-phosphate dehydrogenase HNE, 4-hydroxy-2-nonenal HO-1, heme oxygenase-1 IAA, iodoacetic acid KA, koningic acid mito-15d-PGJ2, mitochondrially targeted 15d-PGJ2 mito-PGE2, mitochondrially targeted prostaglandin E2 NRVM, neonatal rat ventricular myocytes OA, oxamate OCR, oxygen consumption rate PBS, phosphate-buffered saline PPR, proton production rate RASMC, rat aortic smooth muscle cells RNS, reactive nitrogen species ROS, reactive oxygen species siRNA, short-interfering RNA XF, extracellular flux |
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