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Generation of superoxide and hydrogen peroxide by side reactions of mitochondrial 2-oxoacid dehydrogenase complexes in isolation and in cells.
Bunik, Victoria I; Brand, Martin D.
Affiliation
  • Bunik VI; A.N. Belozersky Institute of Physicochemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia.
  • Brand MD; Buck Institute for Research on Aging, 8001 Redwood Blvd., Novato, CA 94945, USA.
Biol Chem ; 399(5): 407-420, 2018 04 25.
Article in En | MEDLINE | ID: mdl-29337692
ABSTRACT
Mitochondrial 2-oxoacid dehydrogenase complexes oxidize 2-oxoglutarate, pyruvate, branched-chain 2-oxoacids and 2-oxoadipate to the corresponding acyl-CoAs and reduce NAD+ to NADH. The isolated enzyme complexes generate superoxide anion radical or hydrogen peroxide in defined reactions by leaking electrons to oxygen. Studies using isolated mitochondria in media mimicking cytosol suggest that the 2-oxoacid dehydrogenase complexes contribute little to the production of superoxide or hydrogen peroxide relative to other mitochondrial sites at physiological steady states. However, the contributions may increase under pathological conditions, in accordance with the high maximum capacities of superoxide or hydrogen peroxide-generating reactions of the complexes, established in isolated mitochondria. We assess available data on the use of modulations of enzyme activity to infer superoxide or hydrogen peroxide production from particular 2-oxoacid dehydrogenase complexes in cells, and limitations of such methods to discriminate specific superoxide or hydrogen peroxide sources in vivo.
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Full text: 1 Database: MEDLINE Main subject: Superoxides / 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide) / Hydrogen Peroxide Limits: Animals / Humans Language: En Year: 2018 Type: Article

Full text: 1 Database: MEDLINE Main subject: Superoxides / 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide) / Hydrogen Peroxide Limits: Animals / Humans Language: En Year: 2018 Type: Article