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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
Institution:
  • 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  d-glucose" target="_blank">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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