Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Luciane
Data de Publicação: 2004
Outros Autores: Silva, Fábio Assunção e [UNIFESP], Kurihara, Rose Saemi, Schor, Nestor [UNIFESP], Higa, Elisa Mieko Suemitsu [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/27596
http://dx.doi.org/10.1111/j.1523-1755.2004.00408.x
Resumo: Background. Radiocontrast agents (RC), substances largely used in diagnostic procedures, present the nephrotoxicity as one of its major side effects, which could be due to an altered synthesis of vasodilators. the aim of the present study was to evaluate the nitric oxide (NO) production in rat renal artery smooth muscle cells primary culture (rVSMC) exposed to RC.Methods. the cells were treated for 72 hours with mannitol at 10% (MT10; 600 mOsm/kg H2O) or 35% (MT35; 2100 mOsm/kg H2O), with the nonionic iobitridol (IBT), the low-osmolality ioxaglate (IXG), the high-osmolality ioxitalamate (IXT), the nonionic, iso-osmolar iodixanol (IDX), and with lipopolysaccharide (LPS). We determined the NO and osmolality in the cell culture media and the cellular viability.Results. By the Griess and chemiluminescence methods, the NO was not different in MT10 and IDX, but decreased in MT35, IBT, IXG, and IXT when compared with the control; it was increased in LPS and also decreased in all RC + LPS when compared with LPS. MT35, IXT, and IXT + LPS decreased the cellular viability, and the media osmolality was increased in MT35 and IXT compared with the control.Conclusion. the RC (except IDX) significantly reduced NO in rVSMC, which was more pronounced after IXT treatment (57.3%). This was not related to the reduced cell viability (15.8%) or to its high osmolality, because in MT35, with similar osmolality as IXT, NO decreased only 11.0% relatively to the control. Neither the media osmolality nor the cell viability was altered by IXG or IBT. the decreased NO could explain the vasoconstriction and, therefore, the acute renal failure by RC.
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spelling Ribeiro, LucianeSilva, Fábio Assunção e [UNIFESP]Kurihara, Rose SaemiSchor, Nestor [UNIFESP]Higa, Elisa Mieko Suemitsu [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2016-01-24T12:34:15Z2016-01-24T12:34:15Z2004-02-01Kidney International. Malden: Blackwell Publishing Inc, v. 65, n. 2, p. 589-596, 2004.0085-2538http://repositorio.unifesp.br/handle/11600/27596http://dx.doi.org/10.1111/j.1523-1755.2004.00408.x10.1111/j.1523-1755.2004.00408.xWOS:000187919500024Background. Radiocontrast agents (RC), substances largely used in diagnostic procedures, present the nephrotoxicity as one of its major side effects, which could be due to an altered synthesis of vasodilators. the aim of the present study was to evaluate the nitric oxide (NO) production in rat renal artery smooth muscle cells primary culture (rVSMC) exposed to RC.Methods. the cells were treated for 72 hours with mannitol at 10% (MT10; 600 mOsm/kg H2O) or 35% (MT35; 2100 mOsm/kg H2O), with the nonionic iobitridol (IBT), the low-osmolality ioxaglate (IXG), the high-osmolality ioxitalamate (IXT), the nonionic, iso-osmolar iodixanol (IDX), and with lipopolysaccharide (LPS). We determined the NO and osmolality in the cell culture media and the cellular viability.Results. By the Griess and chemiluminescence methods, the NO was not different in MT10 and IDX, but decreased in MT35, IBT, IXG, and IXT when compared with the control; it was increased in LPS and also decreased in all RC + LPS when compared with LPS. MT35, IXT, and IXT + LPS decreased the cellular viability, and the media osmolality was increased in MT35 and IXT compared with the control.Conclusion. the RC (except IDX) significantly reduced NO in rVSMC, which was more pronounced after IXT treatment (57.3%). This was not related to the reduced cell viability (15.8%) or to its high osmolality, because in MT35, with similar osmolality as IXT, NO decreased only 11.0% relatively to the control. Neither the media osmolality nor the cell viability was altered by IXG or IBT. the decreased NO could explain the vasoconstriction and, therefore, the acute renal failure by RC.Universidade Federal de São Paulo, Escola Paulista Med, Nephrol & Emergency Div, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Nephrol & Emergency Div, São Paulo, BrazilWeb of Science589-596engBlackwell Publishing IncKidney Internationalradiocontrastnitric oxiderenal arteryvascular smooth muscle cells culturenephrotoxic drugsacute renal failureEvaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agentsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/275962023-01-30 22:17:47.186metadata only accessoai:repositorio.unifesp.br:11600/27596Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-01-31T01:17:47Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
title Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
spellingShingle Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
Ribeiro, Luciane
radiocontrast
nitric oxide
renal artery
vascular smooth muscle cells culture
nephrotoxic drugs
acute renal failure
title_short Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
title_full Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
title_fullStr Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
title_full_unstemmed Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
title_sort Evaluation of the nitric oxide production in rat renal artery smooth muscle cells culture exposed to radiocontrast agents
author Ribeiro, Luciane
author_facet Ribeiro, Luciane
Silva, Fábio Assunção e [UNIFESP]
Kurihara, Rose Saemi
Schor, Nestor [UNIFESP]
Higa, Elisa Mieko Suemitsu [UNIFESP]
author_role author
author2 Silva, Fábio Assunção e [UNIFESP]
Kurihara, Rose Saemi
Schor, Nestor [UNIFESP]
Higa, Elisa Mieko Suemitsu [UNIFESP]
author2_role author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Ribeiro, Luciane
Silva, Fábio Assunção e [UNIFESP]
Kurihara, Rose Saemi
Schor, Nestor [UNIFESP]
Higa, Elisa Mieko Suemitsu [UNIFESP]
dc.subject.eng.fl_str_mv radiocontrast
nitric oxide
renal artery
vascular smooth muscle cells culture
nephrotoxic drugs
acute renal failure
topic radiocontrast
nitric oxide
renal artery
vascular smooth muscle cells culture
nephrotoxic drugs
acute renal failure
description Background. Radiocontrast agents (RC), substances largely used in diagnostic procedures, present the nephrotoxicity as one of its major side effects, which could be due to an altered synthesis of vasodilators. the aim of the present study was to evaluate the nitric oxide (NO) production in rat renal artery smooth muscle cells primary culture (rVSMC) exposed to RC.Methods. the cells were treated for 72 hours with mannitol at 10% (MT10; 600 mOsm/kg H2O) or 35% (MT35; 2100 mOsm/kg H2O), with the nonionic iobitridol (IBT), the low-osmolality ioxaglate (IXG), the high-osmolality ioxitalamate (IXT), the nonionic, iso-osmolar iodixanol (IDX), and with lipopolysaccharide (LPS). We determined the NO and osmolality in the cell culture media and the cellular viability.Results. By the Griess and chemiluminescence methods, the NO was not different in MT10 and IDX, but decreased in MT35, IBT, IXG, and IXT when compared with the control; it was increased in LPS and also decreased in all RC + LPS when compared with LPS. MT35, IXT, and IXT + LPS decreased the cellular viability, and the media osmolality was increased in MT35 and IXT compared with the control.Conclusion. the RC (except IDX) significantly reduced NO in rVSMC, which was more pronounced after IXT treatment (57.3%). This was not related to the reduced cell viability (15.8%) or to its high osmolality, because in MT35, with similar osmolality as IXT, NO decreased only 11.0% relatively to the control. Neither the media osmolality nor the cell viability was altered by IXG or IBT. the decreased NO could explain the vasoconstriction and, therefore, the acute renal failure by RC.
publishDate 2004
dc.date.issued.fl_str_mv 2004-02-01
dc.date.accessioned.fl_str_mv 2016-01-24T12:34:15Z
dc.date.available.fl_str_mv 2016-01-24T12:34:15Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Kidney International. Malden: Blackwell Publishing Inc, v. 65, n. 2, p. 589-596, 2004.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/27596
http://dx.doi.org/10.1111/j.1523-1755.2004.00408.x
dc.identifier.issn.none.fl_str_mv 0085-2538
dc.identifier.doi.none.fl_str_mv 10.1111/j.1523-1755.2004.00408.x
dc.identifier.wos.none.fl_str_mv WOS:000187919500024
identifier_str_mv Kidney International. Malden: Blackwell Publishing Inc, v. 65, n. 2, p. 589-596, 2004.
0085-2538
10.1111/j.1523-1755.2004.00408.x
WOS:000187919500024
url http://repositorio.unifesp.br/handle/11600/27596
http://dx.doi.org/10.1111/j.1523-1755.2004.00408.x
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Kidney International
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 589-596
dc.publisher.none.fl_str_mv Blackwell Publishing Inc
publisher.none.fl_str_mv Blackwell Publishing Inc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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