Mitochondrial function is differentially affected upon oxidative stress

Detalhes bibliográficos
Autor(a) principal: Cardoso, Sandra Morais
Data de Publicação: 1999
Outros Autores: Pereira, Cláudia, Oliveira, Catarina Resende
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/4853
https://doi.org/10.1016/S0891-5849(98)00205-6
Resumo: The mechanisms that lead to mitochondrial damage under oxidative stress conditions were examined in synaptosomes treated with ascorbate/iron. A loss of membrane integrity, evaluated by electron microscopy and by LDH leakage, was observed in peroxidized synaptosomes and it was prevented by pre-incubation with vitamin E (150 [mu]M) and idebenone (50 [mu]M). ATP levels decreased, in synaptosomes exposed to ascorbate/iron, as compared to controls. NADH-ubiquinone oxidoreductase (Cx I) and cytochrome c oxidase (Cx IV) activities were unchanged after ascorbate/iron treatment, whereas succinate-ubiquinone oxidoreductase (Cx II), ubiquinol cytochrome c reductase (Cx III) and ATP-synthase (Cx V) activities were reduced by 55%, 40%, and 55%, respectively. The decrease of complex II and ATP-synthase activities was prevented by reduced glutathione (GSH), whereas the other antioxidants tested (vitamin E and idebenone) were ineffective. However, vitamin E, idebenone and GSH prevented the reduction of complex III activity observed in synaptosomes treated with ascorbate/iron. GSH protective effect suggests that the oxidation of protein SH-groups is involved in the inhibition of complexes II, III and V activity, whereas vitamin E and idebenone protection suggests that membrane lipid peroxidation is also involved in the reduction of complex III activity. These results may indicate that the inhibition of the mitochondrial respiratory chain enzymatic complexes, that are differentially affected by oxidative stress, can be recovered by specific antioxidants.
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spelling Mitochondrial function is differentially affected upon oxidative stressLipid peroxidationSynaptosomesFree radicalsMitochondria respiratory chainAntioxidantsThe mechanisms that lead to mitochondrial damage under oxidative stress conditions were examined in synaptosomes treated with ascorbate/iron. A loss of membrane integrity, evaluated by electron microscopy and by LDH leakage, was observed in peroxidized synaptosomes and it was prevented by pre-incubation with vitamin E (150 [mu]M) and idebenone (50 [mu]M). ATP levels decreased, in synaptosomes exposed to ascorbate/iron, as compared to controls. NADH-ubiquinone oxidoreductase (Cx I) and cytochrome c oxidase (Cx IV) activities were unchanged after ascorbate/iron treatment, whereas succinate-ubiquinone oxidoreductase (Cx II), ubiquinol cytochrome c reductase (Cx III) and ATP-synthase (Cx V) activities were reduced by 55%, 40%, and 55%, respectively. The decrease of complex II and ATP-synthase activities was prevented by reduced glutathione (GSH), whereas the other antioxidants tested (vitamin E and idebenone) were ineffective. However, vitamin E, idebenone and GSH prevented the reduction of complex III activity observed in synaptosomes treated with ascorbate/iron. GSH protective effect suggests that the oxidation of protein SH-groups is involved in the inhibition of complexes II, III and V activity, whereas vitamin E and idebenone protection suggests that membrane lipid peroxidation is also involved in the reduction of complex III activity. These results may indicate that the inhibition of the mitochondrial respiratory chain enzymatic complexes, that are differentially affected by oxidative stress, can be recovered by specific antioxidants.http://www.sciencedirect.com/science/article/B6T38-3VF94NK-1/1/18082880dbbd089b22b9e844e8e20b6f1999info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/4853http://hdl.handle.net/10316/4853https://doi.org/10.1016/S0891-5849(98)00205-6engFree Radical Biology and Medicine. 26:1-2 (1999) 3-13Cardoso, Sandra MoraisPereira, CláudiaOliveira, Catarina Resendeinfo: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:RCAAP2021-10-11T08:54:42Zoai:estudogeral.uc.pt:10316/4853Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:29.378994Repositório 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 Mitochondrial function is differentially affected upon oxidative stress
title Mitochondrial function is differentially affected upon oxidative stress
spellingShingle Mitochondrial function is differentially affected upon oxidative stress
Cardoso, Sandra Morais
Lipid peroxidation
Synaptosomes
Free radicals
Mitochondria respiratory chain
Antioxidants
title_short Mitochondrial function is differentially affected upon oxidative stress
title_full Mitochondrial function is differentially affected upon oxidative stress
title_fullStr Mitochondrial function is differentially affected upon oxidative stress
title_full_unstemmed Mitochondrial function is differentially affected upon oxidative stress
title_sort Mitochondrial function is differentially affected upon oxidative stress
author Cardoso, Sandra Morais
author_facet Cardoso, Sandra Morais
Pereira, Cláudia
Oliveira, Catarina Resende
author_role author
author2 Pereira, Cláudia
Oliveira, Catarina Resende
author2_role author
author
dc.contributor.author.fl_str_mv Cardoso, Sandra Morais
Pereira, Cláudia
Oliveira, Catarina Resende
dc.subject.por.fl_str_mv Lipid peroxidation
Synaptosomes
Free radicals
Mitochondria respiratory chain
Antioxidants
topic Lipid peroxidation
Synaptosomes
Free radicals
Mitochondria respiratory chain
Antioxidants
description The mechanisms that lead to mitochondrial damage under oxidative stress conditions were examined in synaptosomes treated with ascorbate/iron. A loss of membrane integrity, evaluated by electron microscopy and by LDH leakage, was observed in peroxidized synaptosomes and it was prevented by pre-incubation with vitamin E (150 [mu]M) and idebenone (50 [mu]M). ATP levels decreased, in synaptosomes exposed to ascorbate/iron, as compared to controls. NADH-ubiquinone oxidoreductase (Cx I) and cytochrome c oxidase (Cx IV) activities were unchanged after ascorbate/iron treatment, whereas succinate-ubiquinone oxidoreductase (Cx II), ubiquinol cytochrome c reductase (Cx III) and ATP-synthase (Cx V) activities were reduced by 55%, 40%, and 55%, respectively. The decrease of complex II and ATP-synthase activities was prevented by reduced glutathione (GSH), whereas the other antioxidants tested (vitamin E and idebenone) were ineffective. However, vitamin E, idebenone and GSH prevented the reduction of complex III activity observed in synaptosomes treated with ascorbate/iron. GSH protective effect suggests that the oxidation of protein SH-groups is involved in the inhibition of complexes II, III and V activity, whereas vitamin E and idebenone protection suggests that membrane lipid peroxidation is also involved in the reduction of complex III activity. These results may indicate that the inhibition of the mitochondrial respiratory chain enzymatic complexes, that are differentially affected by oxidative stress, can be recovered by specific antioxidants.
publishDate 1999
dc.date.none.fl_str_mv 1999
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/4853
http://hdl.handle.net/10316/4853
https://doi.org/10.1016/S0891-5849(98)00205-6
url http://hdl.handle.net/10316/4853
https://doi.org/10.1016/S0891-5849(98)00205-6
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Free Radical Biology and Medicine. 26:1-2 (1999) 3-13
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dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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