Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , |
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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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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1814268291643867136 |