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


Autoria(s): TAHARA, Erich B.; NAVARETE, Felipe D. T.; KOWALTOWSKI, Alicia J.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

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(2)O(2) release in mitochondria isolated from rat brain, heart, kidney, liver, and skeletal muscle, using various respiratory substrates (alpha-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. (C) 2009 Elsevier Inc. All rights reserved.

Fundocao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

John Simon Guggenhein Memorial Foundation and Conselho Nacional de Pesquisa e Tecnologia (CNPq)

John Simon Guggenhein Memorial Foundation and Conselho Nacional de Pesquisa e Tecnologia (CNPq)

Instituto Nacional de Ciencia e Tecnologia de Processos Redox em Biomedicina (INCT Redoxoma)

Instituto Nacional de Ciencia e Tecnologia de Processos Redox em Biomedicina(INCT Redoxoma)

Identificador

FREE RADICAL BIOLOGY AND MEDICINE, v.46, n.9, p.1283-1297, 2009

0891-5849

http://producao.usp.br/handle/BDPI/30838

10.1016/j.freeradbiomed.2009.02.008

http://dx.doi.org/10.1016/j.freeradbiomed.2009.02.008

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Free Radical Biology and Medicine

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #Mitochondria #Free radical #Respiration #Oxidative stress #Hydrogen peroxide #Superoxide radical #ELECTRON-TRANSPORT CHAIN #SENSITIVE K+-CHANNELS #ALPHA-KETOGLUTARATE DEHYDROGENASE #OXIDOREDUCTASE COMPLEX-I #SKELETAL-MUSCLE CELLS #HYDROGEN-PEROXIDE #SUPEROXIDE-PRODUCTION #CYTOCHROME-C #BRAIN MITOCHONDRIA #HEART-MITOCHONDRIA #Biochemistry & Molecular Biology #Endocrinology & Metabolism
Tipo

article

original article

publishedVersion