Decavanadate contribution to vanadium biomarkers

Detalhes bibliográficos
Autor(a) principal: Aureliano, M.
Data de Publicação: 2016
Tipo de documento: Artigo de conferência
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.1/10267
Resumo: The levels of vanadium in urine and blood can be used as biomarkers of exposure, but the mechanism of vanadium toxicity is of major relevance in order to understand how biomarkes can be valuable. Our research group has performed in vivo and in vitro studies using fish and rat models to analysed and compare the toxicity effects induce by vanadium(V) species in the forms of vanadate (V1) and decavanadate (V10). Vanadium toxicological studies often disregarded the formation of decameric vanadate species (V10) known to interact, in vitro, with high-affinity with many proteins such as myosin, actin and sarcoplasmic reticulum calcium pump. Among different experimental in vivo conditions, it was analysed different: (i) mode of administration; (ii) fish species; (iii) metal concentration (1 and 5 mM); (iv) tissues; (v) subcellular fractions ; (vi) exposure time and particularly different metal ionic species, such as V1 and V10. It was observed that‘‘decavanadate’’ promote different effects than other vanadate oligomers in catalase activity, glutathione content, lipid peroxidation, mitochondrial superoxide anion production and vanadium accumulation. Moreover, in in vitro studies using fish and rat liver mitochondria, it was observed that decavanadate impared respiration by depolarization of the mitochondrial membrane, wich altered the redox state of complex III. Putting it all together, it is suggested that decavanadate species are much more effective than monomeric vanadate species in inducing changes in several biomarkers. By changing mitochondrial functioning decavanadate migh provoke ROS formation, but further studies are needed to understand V10 contribution to vanadium biomarkers.
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spelling Decavanadate contribution to vanadium biomarkersDecavanadateBiomarkersThe levels of vanadium in urine and blood can be used as biomarkers of exposure, but the mechanism of vanadium toxicity is of major relevance in order to understand how biomarkes can be valuable. Our research group has performed in vivo and in vitro studies using fish and rat models to analysed and compare the toxicity effects induce by vanadium(V) species in the forms of vanadate (V1) and decavanadate (V10). Vanadium toxicological studies often disregarded the formation of decameric vanadate species (V10) known to interact, in vitro, with high-affinity with many proteins such as myosin, actin and sarcoplasmic reticulum calcium pump. Among different experimental in vivo conditions, it was analysed different: (i) mode of administration; (ii) fish species; (iii) metal concentration (1 and 5 mM); (iv) tissues; (v) subcellular fractions ; (vi) exposure time and particularly different metal ionic species, such as V1 and V10. It was observed that‘‘decavanadate’’ promote different effects than other vanadate oligomers in catalase activity, glutathione content, lipid peroxidation, mitochondrial superoxide anion production and vanadium accumulation. Moreover, in in vitro studies using fish and rat liver mitochondria, it was observed that decavanadate impared respiration by depolarization of the mitochondrial membrane, wich altered the redox state of complex III. Putting it all together, it is suggested that decavanadate species are much more effective than monomeric vanadate species in inducing changes in several biomarkers. By changing mitochondrial functioning decavanadate migh provoke ROS formation, but further studies are needed to understand V10 contribution to vanadium biomarkers.OMICS InternationalSapientiaAureliano, M.2017-12-21T09:33:09Z20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectapplication/pdfhttp://hdl.handle.net/10400.1/10267eng2471-8556AUT: MAA01296;10.4172/2471-8556.C1.003info: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:RCAAP2023-07-24T10:21:53Zoai:sapientia.ualg.pt:10400.1/10267Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:02:01.317047Repositório 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 Decavanadate contribution to vanadium biomarkers
title Decavanadate contribution to vanadium biomarkers
spellingShingle Decavanadate contribution to vanadium biomarkers
Aureliano, M.
Decavanadate
Biomarkers
title_short Decavanadate contribution to vanadium biomarkers
title_full Decavanadate contribution to vanadium biomarkers
title_fullStr Decavanadate contribution to vanadium biomarkers
title_full_unstemmed Decavanadate contribution to vanadium biomarkers
title_sort Decavanadate contribution to vanadium biomarkers
author Aureliano, M.
author_facet Aureliano, M.
author_role author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Aureliano, M.
dc.subject.por.fl_str_mv Decavanadate
Biomarkers
topic Decavanadate
Biomarkers
description The levels of vanadium in urine and blood can be used as biomarkers of exposure, but the mechanism of vanadium toxicity is of major relevance in order to understand how biomarkes can be valuable. Our research group has performed in vivo and in vitro studies using fish and rat models to analysed and compare the toxicity effects induce by vanadium(V) species in the forms of vanadate (V1) and decavanadate (V10). Vanadium toxicological studies often disregarded the formation of decameric vanadate species (V10) known to interact, in vitro, with high-affinity with many proteins such as myosin, actin and sarcoplasmic reticulum calcium pump. Among different experimental in vivo conditions, it was analysed different: (i) mode of administration; (ii) fish species; (iii) metal concentration (1 and 5 mM); (iv) tissues; (v) subcellular fractions ; (vi) exposure time and particularly different metal ionic species, such as V1 and V10. It was observed that‘‘decavanadate’’ promote different effects than other vanadate oligomers in catalase activity, glutathione content, lipid peroxidation, mitochondrial superoxide anion production and vanadium accumulation. Moreover, in in vitro studies using fish and rat liver mitochondria, it was observed that decavanadate impared respiration by depolarization of the mitochondrial membrane, wich altered the redox state of complex III. Putting it all together, it is suggested that decavanadate species are much more effective than monomeric vanadate species in inducing changes in several biomarkers. By changing mitochondrial functioning decavanadate migh provoke ROS formation, but further studies are needed to understand V10 contribution to vanadium biomarkers.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-01-01T00:00:00Z
2017-12-21T09:33:09Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.1/10267
url http://hdl.handle.net/10400.1/10267
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AUT: MAA01296;
10.4172/2471-8556.C1.003
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dc.publisher.none.fl_str_mv OMICS International
publisher.none.fl_str_mv OMICS International
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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