Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage

Detalhes bibliográficos
Autor(a) principal: Francescato, Heloisa Della Coletta
Data de Publicação: 2011
Outros Autores: Cunha, Fernando Queiroz, Costa, Roberto Silva, Barbosa Junior, Fernando, Boim, Mirian Aparecida [UNIFESP], Arnoni, Carine Prisco [UNIFESP], Alves da Silva, Cleonice Giovanini, Coimbra, Terezila Machado
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1093/ndt/gfq447
http://repositorio.unifesp.br/handle/11600/33390
Resumo: Background. Cisplatin (CP)-induced renal damage is associated with inflammation. Hydrogen sulphide (H(2)S) is involved in models of inflammation. This study evaluates the effect of DL-propargylglycine (PAG), an inhibitor of endogenous H(2)S formation, on the renal damage induced by CP.Methods. the rats were injected with CP (5 mg/kg, i.p.) or PAG(5 mg/kg twice a day, i.p.) for 4 days, starting 1 h before CP injection. Control rats were injected with 0.15 M NaCl or PAG only. Blood and urine samples were collected 5 days after saline or CP injections for renal function evaluation. the kidneys were removed for tumour necrosis factor (TNF)-alpha quantification, histological, immunohistochemical and Western blot analysis. the cystathionine gamma-lyase (CSE) activity and expression were assessed. the direct toxicity of H(2)S in renal tubular cells was evaluated by the incubation of these cells with NaHS, a donor of H(2)S.Results. CP-treated rats presented increases in plasma creatinine levels and in sodium and potassium fractional excretions associated with tubulointerstitial lesions in the outer medulla. Increased expression of TNF-alpha, macrophages, neutrophils and T lymphocytes, associated with increased H(2)S formation rate and CSE expression, were also observed in the outer medulla from CP-injected rats. All these alterations were reduced by treatment with PAG. A direct toxicity of NaHS for renal tubular epithelial cells was not observed.Conclusions. Treatment with PAG reduces the renal damage induced by CP. This effect seems to be related to the H2S formation and the restriction of the inflammation in the kidneys from PAG+CP-treated rats.
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spelling Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damageacute renal failurecisplatinDL-propargylglycinehydrogen sulphideinflammationBackground. Cisplatin (CP)-induced renal damage is associated with inflammation. Hydrogen sulphide (H(2)S) is involved in models of inflammation. This study evaluates the effect of DL-propargylglycine (PAG), an inhibitor of endogenous H(2)S formation, on the renal damage induced by CP.Methods. the rats were injected with CP (5 mg/kg, i.p.) or PAG(5 mg/kg twice a day, i.p.) for 4 days, starting 1 h before CP injection. Control rats were injected with 0.15 M NaCl or PAG only. Blood and urine samples were collected 5 days after saline or CP injections for renal function evaluation. the kidneys were removed for tumour necrosis factor (TNF)-alpha quantification, histological, immunohistochemical and Western blot analysis. the cystathionine gamma-lyase (CSE) activity and expression were assessed. the direct toxicity of H(2)S in renal tubular cells was evaluated by the incubation of these cells with NaHS, a donor of H(2)S.Results. CP-treated rats presented increases in plasma creatinine levels and in sodium and potassium fractional excretions associated with tubulointerstitial lesions in the outer medulla. Increased expression of TNF-alpha, macrophages, neutrophils and T lymphocytes, associated with increased H(2)S formation rate and CSE expression, were also observed in the outer medulla from CP-injected rats. All these alterations were reduced by treatment with PAG. A direct toxicity of NaHS for renal tubular epithelial cells was not observed.Conclusions. Treatment with PAG reduces the renal damage induced by CP. This effect seems to be related to the H2S formation and the restriction of the inflammation in the kidneys from PAG+CP-treated rats.Univ São Paulo, Fac Med Ribeirao Preto, Dept Physiol, São Paulo, BrazilUniv São Paulo, Fac Med Ribeirao Preto, Dept Pharmacol, São Paulo, BrazilUniv São Paulo, Fac Med Ribeirao Preto, Dept Pathol, São Paulo, BrazilUniv São Paulo, Fac Pharmaceut Sci Ribeirao Preto, Dept Clin Toxicol & Bromatol Anal, São Paulo, BrazilUniversidade Federal de São Paulo, Div Renal, Dept Med, São Paulo, BrazilDepartment of Medicine, Renal Division, Federal University of São Paulo, São Paulo, BrazilWeb of ScienceConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Oxford Univ PressUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Francescato, Heloisa Della ColettaCunha, Fernando QueirozCosta, Roberto SilvaBarbosa Junior, FernandoBoim, Mirian Aparecida [UNIFESP]Arnoni, Carine Prisco [UNIFESP]Alves da Silva, Cleonice GiovaniniCoimbra, Terezila Machado2016-01-24T14:06:05Z2016-01-24T14:06:05Z2011-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion479-488http://dx.doi.org/10.1093/ndt/gfq447Nephrology Dialysis Transplantation. Oxford: Oxford Univ Press, v. 26, n. 2, p. 479-488, 2011.10.1093/ndt/gfq4470931-0509http://repositorio.unifesp.br/handle/11600/33390WOS:000286675400014engNephrology Dialysis Transplantationinfo:eu-repo/semantics/openAccesshttp://www.oxfordjournals.org/access_purchase/self-archiving_policyb.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-07-08T10:22:09Zoai:repositorio.unifesp.br/:11600/33390Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-07-08T10:22:09Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
title Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
spellingShingle Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
Francescato, Heloisa Della Coletta
acute renal failure
cisplatin
DL-propargylglycine
hydrogen sulphide
inflammation
title_short Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
title_full Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
title_fullStr Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
title_full_unstemmed Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
title_sort Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
author Francescato, Heloisa Della Coletta
author_facet Francescato, Heloisa Della Coletta
Cunha, Fernando Queiroz
Costa, Roberto Silva
Barbosa Junior, Fernando
Boim, Mirian Aparecida [UNIFESP]
Arnoni, Carine Prisco [UNIFESP]
Alves da Silva, Cleonice Giovanini
Coimbra, Terezila Machado
author_role author
author2 Cunha, Fernando Queiroz
Costa, Roberto Silva
Barbosa Junior, Fernando
Boim, Mirian Aparecida [UNIFESP]
Arnoni, Carine Prisco [UNIFESP]
Alves da Silva, Cleonice Giovanini
Coimbra, Terezila Machado
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Francescato, Heloisa Della Coletta
Cunha, Fernando Queiroz
Costa, Roberto Silva
Barbosa Junior, Fernando
Boim, Mirian Aparecida [UNIFESP]
Arnoni, Carine Prisco [UNIFESP]
Alves da Silva, Cleonice Giovanini
Coimbra, Terezila Machado
dc.subject.por.fl_str_mv acute renal failure
cisplatin
DL-propargylglycine
hydrogen sulphide
inflammation
topic acute renal failure
cisplatin
DL-propargylglycine
hydrogen sulphide
inflammation
description Background. Cisplatin (CP)-induced renal damage is associated with inflammation. Hydrogen sulphide (H(2)S) is involved in models of inflammation. This study evaluates the effect of DL-propargylglycine (PAG), an inhibitor of endogenous H(2)S formation, on the renal damage induced by CP.Methods. the rats were injected with CP (5 mg/kg, i.p.) or PAG(5 mg/kg twice a day, i.p.) for 4 days, starting 1 h before CP injection. Control rats were injected with 0.15 M NaCl or PAG only. Blood and urine samples were collected 5 days after saline or CP injections for renal function evaluation. the kidneys were removed for tumour necrosis factor (TNF)-alpha quantification, histological, immunohistochemical and Western blot analysis. the cystathionine gamma-lyase (CSE) activity and expression were assessed. the direct toxicity of H(2)S in renal tubular cells was evaluated by the incubation of these cells with NaHS, a donor of H(2)S.Results. CP-treated rats presented increases in plasma creatinine levels and in sodium and potassium fractional excretions associated with tubulointerstitial lesions in the outer medulla. Increased expression of TNF-alpha, macrophages, neutrophils and T lymphocytes, associated with increased H(2)S formation rate and CSE expression, were also observed in the outer medulla from CP-injected rats. All these alterations were reduced by treatment with PAG. A direct toxicity of NaHS for renal tubular epithelial cells was not observed.Conclusions. Treatment with PAG reduces the renal damage induced by CP. This effect seems to be related to the H2S formation and the restriction of the inflammation in the kidneys from PAG+CP-treated rats.
publishDate 2011
dc.date.none.fl_str_mv 2011-02-01
2016-01-24T14:06:05Z
2016-01-24T14:06:05Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1093/ndt/gfq447
Nephrology Dialysis Transplantation. Oxford: Oxford Univ Press, v. 26, n. 2, p. 479-488, 2011.
10.1093/ndt/gfq447
0931-0509
http://repositorio.unifesp.br/handle/11600/33390
WOS:000286675400014
url http://dx.doi.org/10.1093/ndt/gfq447
http://repositorio.unifesp.br/handle/11600/33390
identifier_str_mv Nephrology Dialysis Transplantation. Oxford: Oxford Univ Press, v. 26, n. 2, p. 479-488, 2011.
10.1093/ndt/gfq447
0931-0509
WOS:000286675400014
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Nephrology Dialysis Transplantation
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html
dc.format.none.fl_str_mv 479-488
dc.publisher.none.fl_str_mv Oxford Univ Press
publisher.none.fl_str_mv Oxford Univ Press
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 biblioteca.csp@unifesp.br
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