Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study

Detalhes bibliográficos
Autor(a) principal: Fernandes, M. A. S.
Data de Publicação: 2002
Outros Autores: Santos, M. S., Alpoim, M. C., Madeira, V. M. C., Vicente, J. A. F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8343
https://doi.org/10.1002/jbt.10025
Resumo: The mechanism of Cr(VI)-induced toxicity in plants and animals has been assessed for mitochondrial bioenergetics and membrane damage in turnip root and rat liver mitochondria. By using succinate as the respiratory substrate, ADP/O and respiratory control ratio (RCR) were depressed as a function of Cr(VI) concentration. State 3 and uncoupled respiration were also depressed by Cr(VI). Rat mitochondria revealed a higher sensitivity to Cr(VI), as compared to turnip mitochondria. Rat mitochondrial state 4 respiration rate triplicated in contrast to negligible stimulation of turnip state 4 respiration. Chromium(VI) inhibited the activity of the NADH-ubiquinone oxidoreductase (complex I) from rat liver mitochondria and succinate-dehydrogenases (complex II) from plant and animal mitochondria. In rat liver mitochondria, complex I was more sensitive to Cr(VI) than complex II. The activity of cytochrome c oxidase (complex IV) was not sensitive to Cr(VI). Unique for plant mitochondria, exogenous NADH uncoupled respiration was unaffected by Cr(VI), indicating that the NADH dehydrogenase of the outer leaflet of the plant inner membrane, in addition to complexes III and IV, were insensitive to Cr(VI). The ATPase activity (complex V) was stimulated in rat liver mitochondria, but inhibited in turnip root mitochondria. In both, turnip and rat mitochondria, Cr(VI) depressed mitochondrial succinate-dependent transmembrane potential (Deltapsi) and phosphorylation efficiency, but it neither affected mitochondrial membrane permeabilization to protons (H+) nor induced membrane lipid peroxidation. However, Cr(VI) induced mitochondrial membrane permeabilization to K+, an effect that was more pronounced in turnip root than in rat liver mitochondria. In conclusion, Cr(VI)-induced perturbations of mitochondrial bioenergetics compromises energy-dependent biochemical processes and, therefore, may contribute to the basal mechanism underlying its toxic effects in plant and animal cells. © 2002 Wiley Periodicals, Inc. J Biochem Mol Toxicol 16:53-63, 2002; Published online in Wiley Interscience (www.interscience.wiley.com). DOI 10.1002/jbt.10025
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spelling Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative studyThe mechanism of Cr(VI)-induced toxicity in plants and animals has been assessed for mitochondrial bioenergetics and membrane damage in turnip root and rat liver mitochondria. By using succinate as the respiratory substrate, ADP/O and respiratory control ratio (RCR) were depressed as a function of Cr(VI) concentration. State 3 and uncoupled respiration were also depressed by Cr(VI). Rat mitochondria revealed a higher sensitivity to Cr(VI), as compared to turnip mitochondria. Rat mitochondrial state 4 respiration rate triplicated in contrast to negligible stimulation of turnip state 4 respiration. Chromium(VI) inhibited the activity of the NADH-ubiquinone oxidoreductase (complex I) from rat liver mitochondria and succinate-dehydrogenases (complex II) from plant and animal mitochondria. In rat liver mitochondria, complex I was more sensitive to Cr(VI) than complex II. The activity of cytochrome c oxidase (complex IV) was not sensitive to Cr(VI). Unique for plant mitochondria, exogenous NADH uncoupled respiration was unaffected by Cr(VI), indicating that the NADH dehydrogenase of the outer leaflet of the plant inner membrane, in addition to complexes III and IV, were insensitive to Cr(VI). The ATPase activity (complex V) was stimulated in rat liver mitochondria, but inhibited in turnip root mitochondria. In both, turnip and rat mitochondria, Cr(VI) depressed mitochondrial succinate-dependent transmembrane potential (Deltapsi) and phosphorylation efficiency, but it neither affected mitochondrial membrane permeabilization to protons (H+) nor induced membrane lipid peroxidation. However, Cr(VI) induced mitochondrial membrane permeabilization to K+, an effect that was more pronounced in turnip root than in rat liver mitochondria. In conclusion, Cr(VI)-induced perturbations of mitochondrial bioenergetics compromises energy-dependent biochemical processes and, therefore, may contribute to the basal mechanism underlying its toxic effects in plant and animal cells. © 2002 Wiley Periodicals, Inc. J Biochem Mol Toxicol 16:53-63, 2002; Published online in Wiley Interscience (www.interscience.wiley.com). DOI 10.1002/jbt.100252002info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8343http://hdl.handle.net/10316/8343https://doi.org/10.1002/jbt.10025engJournal of Biochemical and Molecular Toxicology. 16:2 (2002) 53-63Fernandes, M. A. S.Santos, M. S.Alpoim, M. C.Madeira, V. M. C.Vicente, J. A. F.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-11-09T10:11:56Zoai:estudogeral.uc.pt:10316/8343Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:32.176122Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
title Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
spellingShingle Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
Fernandes, M. A. S.
title_short Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
title_full Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
title_fullStr Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
title_full_unstemmed Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
title_sort Chromium(VI) interaction with plant and animal mitochondrial bioenergetics: A comparative study
author Fernandes, M. A. S.
author_facet Fernandes, M. A. S.
Santos, M. S.
Alpoim, M. C.
Madeira, V. M. C.
Vicente, J. A. F.
author_role author
author2 Santos, M. S.
Alpoim, M. C.
Madeira, V. M. C.
Vicente, J. A. F.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Fernandes, M. A. S.
Santos, M. S.
Alpoim, M. C.
Madeira, V. M. C.
Vicente, J. A. F.
description The mechanism of Cr(VI)-induced toxicity in plants and animals has been assessed for mitochondrial bioenergetics and membrane damage in turnip root and rat liver mitochondria. By using succinate as the respiratory substrate, ADP/O and respiratory control ratio (RCR) were depressed as a function of Cr(VI) concentration. State 3 and uncoupled respiration were also depressed by Cr(VI). Rat mitochondria revealed a higher sensitivity to Cr(VI), as compared to turnip mitochondria. Rat mitochondrial state 4 respiration rate triplicated in contrast to negligible stimulation of turnip state 4 respiration. Chromium(VI) inhibited the activity of the NADH-ubiquinone oxidoreductase (complex I) from rat liver mitochondria and succinate-dehydrogenases (complex II) from plant and animal mitochondria. In rat liver mitochondria, complex I was more sensitive to Cr(VI) than complex II. The activity of cytochrome c oxidase (complex IV) was not sensitive to Cr(VI). Unique for plant mitochondria, exogenous NADH uncoupled respiration was unaffected by Cr(VI), indicating that the NADH dehydrogenase of the outer leaflet of the plant inner membrane, in addition to complexes III and IV, were insensitive to Cr(VI). The ATPase activity (complex V) was stimulated in rat liver mitochondria, but inhibited in turnip root mitochondria. In both, turnip and rat mitochondria, Cr(VI) depressed mitochondrial succinate-dependent transmembrane potential (Deltapsi) and phosphorylation efficiency, but it neither affected mitochondrial membrane permeabilization to protons (H+) nor induced membrane lipid peroxidation. However, Cr(VI) induced mitochondrial membrane permeabilization to K+, an effect that was more pronounced in turnip root than in rat liver mitochondria. In conclusion, Cr(VI)-induced perturbations of mitochondrial bioenergetics compromises energy-dependent biochemical processes and, therefore, may contribute to the basal mechanism underlying its toxic effects in plant and animal cells. © 2002 Wiley Periodicals, Inc. J Biochem Mol Toxicol 16:53-63, 2002; Published online in Wiley Interscience (www.interscience.wiley.com). DOI 10.1002/jbt.10025
publishDate 2002
dc.date.none.fl_str_mv 2002
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8343
http://hdl.handle.net/10316/8343
https://doi.org/10.1002/jbt.10025
url http://hdl.handle.net/10316/8343
https://doi.org/10.1002/jbt.10025
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv Journal of Biochemical and Molecular Toxicology. 16:2 (2002) 53-63
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