Superoxide production is inversely related to complex I activity in inherited complex I deficiency.
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SourceBiochimica et Biophysica Acta. Molecular Basis of Disease, 1772, 3, (2007), pp. 373-81
Article / Letter to editor
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Paediatrics - OUD tm 2017
Biochimica et Biophysica Acta. Molecular Basis of Disease
SubjectIGMD 8: Mitochondrial medicine; IGMD 9: Renal disorder; NCMLS 2: Metabolism, transport and motion; NCMLS 4: Energy and redox metabolism; UMCN 5.3: Cellular energy metabolism; UMCN 5.4: Renal disorders
Deficiency of NADH:ubiquinone oxidoreductase or complex I (CI) is the most common cause of disorders of the oxidative phosphorylation system in humans. Using life cell imaging and blue-native electrophoresis we quantitatively compared superoxide production and CI amount and activity in cultured skin fibroblasts of 7 healthy control subjects and 21 children with inherited isolated CI deficiency. Thirteen children had a disease causing mutation in one of the nuclear-encoded CI subunits, whereas in the remainder the genetic cause of the disease is not yet established. Superoxide production was significantly increased in all but two of the patient cell lines. An inverse relationship with the amount and residual activity of CI was observed. In agreement with this finding, rotenone, a potent inhibitor of CI activity, dose-dependently increased superoxide production in healthy control cells. Also in this case an inverse relationship with the residual activity of CI was observed. In sharp contrast, however, rotenone did not decrease the amount of CI. The data presented show that superoxide production is increased in inherited CI deficiency and that this increase is primarily a consequence of the reduction in cellular CI activity and not of a further leakage of electrons from mutationally malformed complexes.
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