Assessing bioenergetic function in response to oxidative stress by metabolic profiling

被引:359
作者
Dranka, Brian P. [1 ,2 ]
Benavides, Gloria A. [1 ,2 ]
Diers, Anne R. [1 ,2 ]
Giordano, Samantha [1 ,2 ]
Zelickson, Blake R. [1 ,2 ]
Reily, Colin [1 ,2 ]
Zou, Luyun [1 ,2 ]
Chatham, John C. [1 ,2 ]
Hill, Bradford G. [3 ]
Zhang, Jianhua [1 ,2 ]
Landar, Aimee [1 ,2 ]
Darley-Usmar, Victor M. [1 ,2 ]
机构
[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Ctr Free Rad Biol, Birmingham, AL 35294 USA
[3] Univ Louisville, Dept Cardiovasc Med, Louisville, KY 40202 USA
关键词
Extracellular flux; Oxygen consumption rate; Mitochondrial profile; Reserve capacity; Mitochondria; Oxidative stress; Nitric oxide; 4-Hydroxynonenal; Free radicals; CYTOCHROME-C RELEASE; NITRIC-OXIDE; 15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2); MITOCHONDRIAL DYSFUNCTION; ENDOTHELIAL-CELLS; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; CELLULAR BIOENERGETICS; PROTEIN; ACTIVATION; INHIBITION;
D O I
10.1016/j.freeradbiomed.2011.08.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1621 / 1635
页数:15
相关论文
共 73 条
[1]  
[Anonymous], 2002, BIOENERGETICS
[2]   Mitochondrial dysfunction in cardiovascular disease [J].
Ballinger, SW .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 38 (10) :1278-1295
[3]   Loss of ischemic preconditioning's cardioprotection in aged mouse hearts is associated with reduced gap junctional and mitochondrial levels of connexin 43 [J].
Boengler, Kerstin ;
Konietzka, Ina ;
Buechert, Astrid ;
Heinen, Yvonne ;
Garcia-Dorado, David ;
Heusch, Gerd ;
Schulz, Rainer .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 292 (04) :H1764-H1769
[4]   Nitric oxide induces apoptosis via hydrogen peroxide, but necrosis via energy and thiol depletion [J].
Borutaite, V ;
Brown, GC .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (11) :1457-1468
[5]   Assessing mitochondrial dysfunction in cells [J].
Brand, Martin D. ;
Nicholls, David G. .
BIOCHEMICAL JOURNAL, 2011, 435 :297-312
[6]   FLUOROCITRATE INHIBITION OF ACONITATE HYDRATASE AND TRICARBOXYLATE CARRIER OF RAT-LIVER MITOCHONDRIA [J].
BRAND, MD ;
EVANS, SM ;
MENDESMO.J ;
CHAPPELL, JB .
BIOCHEMICAL JOURNAL, 1973, 134 (01) :217-224
[7]   Bioenergetic analysis of isolated cerebrocortical nerve terminals on a microgram scale: spare respiratory capacity and stochastic mitochondrial failure [J].
Choi, Sung W. ;
Gerencser, Akos A. ;
Nicholls, David G. .
JOURNAL OF NEUROCHEMISTRY, 2009, 109 (04) :1179-1191
[8]   Interference and blood sample preparation for a pyruvate enzymatic assay [J].
Chuang, CK ;
Wang, TJ ;
Yeung, CY ;
Hsieh, WS ;
Lin, DS ;
Ho, SC ;
Lin, SP .
CLINICAL BIOCHEMISTRY, 2006, 39 (01) :74-77
[9]   CONTINUOUS RECORDING OF BLOOD OXYGEN TENSIONS BY POLAROGRAPHY [J].
CLARK, LC ;
WOLF, R ;
GRANGER, D ;
TAYLOR, Z .
JOURNAL OF APPLIED PHYSIOLOGY, 1953, 6 (03) :189-193
[10]   REVERSIBLE INHIBITION OF CYTOCHROME-C-OXIDASE, THE TERMINAL ENZYME OF THE MITOCHONDRIAL RESPIRATORY-CHAIN, BY NITRIC-OXIDE - IMPLICATIONS FOR NEURODEGENERATIVE DISEASES [J].
CLEETER, MWJ ;
COOPER, JM ;
DARLEYUSMAR, VM ;
MONCADA, S ;
SCHAPIRA, AHV .
FEBS LETTERS, 1994, 345 (01) :50-54