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Assessing bioenergetic function in response to oxidative stress by metabolic profiling
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
Affiliation:
  • a Department of Pathology and Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA
  • b Department of Cardiovascular Medicine, University of Louisville, Louisville, KY 40202, USA
  • 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.
    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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