Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications

Detalhes bibliográficos
Autor(a) principal: Augusto,Ohara
Data de Publicação: 2008
Outros Autores: Trindade,Daniel F., Linares,Edlaine, Vaz,Sandra M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Anais da Academia Brasileira de Ciências (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652008000100013
Resumo: The substantial therapeutic potential of tempol (4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy) and related cyclic nitroxides as antioxidants has stimulated innumerous studies of their reactions with reactive oxygen species. In comparison, reactions of nitroxides with nitric oxide-derived oxidants have been less frequently investigated. Nevertheless, this is relevant because tempol has also been shown to protect animals from injuries associated with inflammatory conditions, which are characterized by the increased production of nitric oxide and its derived oxidants. Here, we review recent studies addressing the mechanisms by which cyclic nitroxides attenuate the toxicity of nitric oxidederived oxidants. As an example, we present data showing that tempol protects mice from acetaminophen-induced hepatotoxicity and discuss the possible protection mechanism. In view of the summarized studies, it is proposed that nitroxides attenuate tissue injury under inflammatory conditions mainly because of their ability to react rapidly with nitrogen dioxide and carbonate radical. In the process the nitroxides are oxidized to the corresponding oxammonium cation, which, in turn, can be recycled back to the nitroxides by reacting with upstream species, such as peroxynitrite and hydrogen peroxide, or with cellular reductants. An auxiliary protection mechanism may be down-regulation of inducible nitric oxide synthase expression. The possible therapeutic implications of these mechanisms are addressed.
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spelling Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implicationscyclic nitroxidestempolantioxidantsnitric oxide-derived oxidantsinflammationacetaminopheninduced hepatotoxicityThe substantial therapeutic potential of tempol (4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy) and related cyclic nitroxides as antioxidants has stimulated innumerous studies of their reactions with reactive oxygen species. In comparison, reactions of nitroxides with nitric oxide-derived oxidants have been less frequently investigated. Nevertheless, this is relevant because tempol has also been shown to protect animals from injuries associated with inflammatory conditions, which are characterized by the increased production of nitric oxide and its derived oxidants. Here, we review recent studies addressing the mechanisms by which cyclic nitroxides attenuate the toxicity of nitric oxidederived oxidants. As an example, we present data showing that tempol protects mice from acetaminophen-induced hepatotoxicity and discuss the possible protection mechanism. In view of the summarized studies, it is proposed that nitroxides attenuate tissue injury under inflammatory conditions mainly because of their ability to react rapidly with nitrogen dioxide and carbonate radical. In the process the nitroxides are oxidized to the corresponding oxammonium cation, which, in turn, can be recycled back to the nitroxides by reacting with upstream species, such as peroxynitrite and hydrogen peroxide, or with cellular reductants. An auxiliary protection mechanism may be down-regulation of inducible nitric oxide synthase expression. The possible therapeutic implications of these mechanisms are addressed.Academia Brasileira de Ciências2008-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652008000100013Anais da Academia Brasileira de Ciências v.80 n.1 2008reponame:Anais da Academia Brasileira de Ciências (Online)instname:Academia Brasileira de Ciências (ABC)instacron:ABC10.1590/S0001-37652008000100013info:eu-repo/semantics/openAccessAugusto,OharaTrindade,Daniel F.Linares,EdlaineVaz,Sandra M.eng2008-03-10T00:00:00Zoai:scielo:S0001-37652008000100013Revistahttp://www.scielo.br/aabchttps://old.scielo.br/oai/scielo-oai.php||aabc@abc.org.br1678-26900001-3765opendoar:2008-03-10T00:00Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC)false
dc.title.none.fl_str_mv Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
title Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
spellingShingle Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
Augusto,Ohara
cyclic nitroxides
tempol
antioxidants
nitric oxide-derived oxidants
inflammation
acetaminopheninduced hepatotoxicity
title_short Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
title_full Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
title_fullStr Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
title_full_unstemmed Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
title_sort Cyclic nitroxides inhibit the toxicity of nitric oxide-derived oxidants: mechanisms and implications
author Augusto,Ohara
author_facet Augusto,Ohara
Trindade,Daniel F.
Linares,Edlaine
Vaz,Sandra M.
author_role author
author2 Trindade,Daniel F.
Linares,Edlaine
Vaz,Sandra M.
author2_role author
author
author
dc.contributor.author.fl_str_mv Augusto,Ohara
Trindade,Daniel F.
Linares,Edlaine
Vaz,Sandra M.
dc.subject.por.fl_str_mv cyclic nitroxides
tempol
antioxidants
nitric oxide-derived oxidants
inflammation
acetaminopheninduced hepatotoxicity
topic cyclic nitroxides
tempol
antioxidants
nitric oxide-derived oxidants
inflammation
acetaminopheninduced hepatotoxicity
description The substantial therapeutic potential of tempol (4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy) and related cyclic nitroxides as antioxidants has stimulated innumerous studies of their reactions with reactive oxygen species. In comparison, reactions of nitroxides with nitric oxide-derived oxidants have been less frequently investigated. Nevertheless, this is relevant because tempol has also been shown to protect animals from injuries associated with inflammatory conditions, which are characterized by the increased production of nitric oxide and its derived oxidants. Here, we review recent studies addressing the mechanisms by which cyclic nitroxides attenuate the toxicity of nitric oxidederived oxidants. As an example, we present data showing that tempol protects mice from acetaminophen-induced hepatotoxicity and discuss the possible protection mechanism. In view of the summarized studies, it is proposed that nitroxides attenuate tissue injury under inflammatory conditions mainly because of their ability to react rapidly with nitrogen dioxide and carbonate radical. In the process the nitroxides are oxidized to the corresponding oxammonium cation, which, in turn, can be recycled back to the nitroxides by reacting with upstream species, such as peroxynitrite and hydrogen peroxide, or with cellular reductants. An auxiliary protection mechanism may be down-regulation of inducible nitric oxide synthase expression. The possible therapeutic implications of these mechanisms are addressed.
publishDate 2008
dc.date.none.fl_str_mv 2008-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652008000100013
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652008000100013
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0001-37652008000100013
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Academia Brasileira de Ciências
publisher.none.fl_str_mv Academia Brasileira de Ciências
dc.source.none.fl_str_mv Anais da Academia Brasileira de Ciências v.80 n.1 2008
reponame:Anais da Academia Brasileira de Ciências (Online)
instname:Academia Brasileira de Ciências (ABC)
instacron:ABC
instname_str Academia Brasileira de Ciências (ABC)
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reponame_str Anais da Academia Brasileira de Ciências (Online)
collection Anais da Academia Brasileira de Ciências (Online)
repository.name.fl_str_mv Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC)
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