Cited by 28Mitochondrial Function and PathologyRedox biology and oxidative stressBioactive Compounds and Antitumor Agents

The respiratory-chain poison antimycin A promotes the formation of DNA single-strand breaks and reduces toxicity in U937 cells exposed to t-butylhydroperoxide

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GUIDARELLI, Andrea, BRAMBILLA, Liliana, ROTA, Cristina, TOMASI, Aldo, CATTABENI, Flaminio, CANTONI, Orazio·1996·Biochemical Journal

Abstract

Antimycin A at levels that abolish oxygen consumption had a slight, although statistically significant, inhibitory effect on the toxicity elicited by t-butylhydroperoxide in U937 cells. The protective effect was observed after 6 h of post-treatment incubation, but was no longer apparent after 24 h. Unexpectedly, these events were associated with a marked accumulation of DNA single-strand breaks produced by low levels of t-butylhydroperoxide. Both an oxygen- and a carbon-centred radical were found to arise during treatment with t-butylhydroperoxide, and their formation was significantly lowered by antimycin A. Thus inhibition of electron transport at the level of complex III appears (a) to decrease the formation of toxic species which mediate, at least partially, the lethal effects elicited by t-butylhydroperoxide, and (b) to enhance the formation of DNA-damaging species generated at low concentrations of t-butylhydroperoxide. Rotenone and cyanide, which respectively inhibit complexes I and IV, did not affect DNA damage elicited by t-butylhydroperoxide. These results suggest that DNA single-strand breaks do not mediate the toxicity of t-butylhydroperoxide, and that specific mitochondrial functions might modulate the formation of toxic and of DNA-damaging species generated by organic hydroperoxides.

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Crossref · 10.1042/bj3170371

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Authors
GUIDARELLI, A., BRAMBILLA, L., ROTA, C., TOMASI, A., CATTABENI, F., & CANTONI, O.
Affiliations
  • University of Urbino (IT)
  • University of Modena and Reggio Emilia (IT)
Venue
Biochemical Journal
Published
1996-07-15
Volume
317
Issue
2
Pages
371-375
ISSN
  • 0264-6021 (ISSN-L)
  • 1470-8728
OpenAlex
W272280634
Cited by
28
References
17
Citations by year
2024: 1 · 2021: 1 · 2020: 1
FWCI
1.64
Type
journal article
Language
en
Open access
Locations
  • Biochemical Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Bioactive Compounds and Antitumor Agents
Keywords
antimycin A, tert-butyl hydroperoxide, single-strand breaks, U937 cells, oxidative DNA damage, organic hydroperoxides, oxygen-centred radicals, carbon-centered radicals, rotenone, cyanide, mitochondrial function, cytotoxicity
MeSH terms
Antimycin A, Cells, Cultured, DNA Damage, DNA Repair, Dose-Response Relationship, Drug, Electron Spin Resonance Spectroscopy, Electron Transport, Enzyme Inhibitors, Humans, Mitochondria, Peroxides, Reactive Oxygen Species, Toxicity Tests, tert-Butylhydroperoxide

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