Journal
FREE RADICAL BIOLOGY AND MEDICINE
Volume 49, Issue 12, Pages 1903-1915Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2010.09.020
Keywords
Chromate; Chromium(VI); Mitochondria; Iron-sulfur proteins; Aconitase; Complex I; Complex II; Free radicals
Funding
- National Institute of Environmental Health Sciences (NIEHS) NIH [ES012707]
- NIH [EB001980]
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Hexavalent chromium (Cr(VI)) compounds (e g chromates) are strong oxidants that readily enter cells where they are reduced to reactive Cr species that also facilitate reactive oxygen species generation Recent studies demonstrated inhibition and oxidation of the thioredoxin system with greater effects on mitochondrial thioredoxin (Trx2) This implies that Cr(VI) induced oxidant stress may be especially directed at the mitochondria Examination of other redox-sensitive mitochondrial functions showed that Cr(VI) treatments that cause Trx2 oxidation in human bronchial epithelial cells also result in pronounced and irreversible inhibition of aconitase a TCA cycle enzyme that has an iron-sulfur (Fe-S) center that is labile with respect to certain oxidants The activities of electron transport complexes I and II were also inhibited whereas complex III was not Electron paramagnetic resonance (EPR) studies of samples at liquid helium temperature (10 K) showed a strong signal at g=1 94 that is consistent with the inhibition of electron flow through complex I and/or II A signal at g=2 02 was also observed which is consistent with oxidation of the Fe-S center of aconitase The g=1 94 signal was particularly intense and remained after extracellular Cr(VI) was removed whereas the g=2 02 signal declined in intensity after Cr(VI) was removed A similar inhibition of these activities and analogous EPR findings were noted in bovine airways treated ex vivo with Cr(VI) Overall the data support the hypothesis that Cr(VI) exposure has deleterious effects on a number of redox-sensitive core mitochondrial proteins The g=1 94 signal could prove to be an important biomarker for oxidative damage resulting from Cr(VI) exposure The EPR spectra simultaneously showed signals for Cr(V) and Cr(III) which verify Cr(VI) exposure and its intracellular reductive activation (C) 2010 Elsevier Inc All rights reserved
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