Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats

Detalhes bibliográficos
Autor(a) principal: Baracho,Nilo César do Vale
Data de Publicação: 2017
Outros Autores: Silveira,Kátia Daniela da, Rocha,Natália Pessoa, Cordeiro,Thiago Macedo, Feracin,Victor, Pereira,Regina Maria, Reis,Marconi Augusto Aguiar dos, Teixeira,Mauro Martins, Silva,Ana Cristina Simões e
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal Brasileiro de Nefrologia
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000200108
Resumo: Abstract Introduction: It is still unknown how the pharmacological inhibition of the Renin Angiotensin System (RAS) impacts the levels of inflammation and fibrosis biomarkers. Objective: This study sought to evaluate the effect of enalapril, candesartan and aliskiren on urinary levels of cytokines in a model of chronic kidney disease (CKD). Methods: Male Wistar rats were submitted to surgical removal of ¾ of renal parenchyma to induce CKD (¾ nephrectomy), or subjected to sham surgery (control). Animals were then randomized into five groups: Sham surgery receiving vehicle; ¾ Nephrectomy receiving vehicle; ¾ Nephrectomy receiving enalapril (10 mg/kg); ¾ Nephrectomy receiving candesartan (10 mg/kg) and ¾ Nephrectomy receiving aliskiren (10 mg/kg). Urine output, water intake, mean arterial pressure (MAP) and urinary concentrations of creatinine, urea, albuminuria, Na+, K+, interleukin (IL) -1β, IL-6, IL-10 and transforming growth factor beta (TGF-β) were measured. Results: Nephrectomy significantly impaired renal function, increased MAP and altered the levels of all evaluated cytokines in urine. Enalapril, candesartan and aliskiren improved renal function and decreased MAP and IL-6 when compared to vehicle-treated nephrectomized group. Candesartan and aliskiren decreased IL-1β, while only candesartan reduced TGF-β and only aliskiren increased IL-10. Conclusion: Enalapril, candesartan and aliskiren presented similar effects on improving renal function and reducing MAP and urinary levels of IL-6 in rats with CKD. On the other hand, cytokine profile differed according to the treatment, suggesting that differential mechanisms were triggered in response to the site of RAS blockade.
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spelling Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized ratsangiotensinsangiotensin-converting enzyme inhibitorsangiotensin receptor antagonistskidney failure, chronicnephrectomyAbstract Introduction: It is still unknown how the pharmacological inhibition of the Renin Angiotensin System (RAS) impacts the levels of inflammation and fibrosis biomarkers. Objective: This study sought to evaluate the effect of enalapril, candesartan and aliskiren on urinary levels of cytokines in a model of chronic kidney disease (CKD). Methods: Male Wistar rats were submitted to surgical removal of ¾ of renal parenchyma to induce CKD (¾ nephrectomy), or subjected to sham surgery (control). Animals were then randomized into five groups: Sham surgery receiving vehicle; ¾ Nephrectomy receiving vehicle; ¾ Nephrectomy receiving enalapril (10 mg/kg); ¾ Nephrectomy receiving candesartan (10 mg/kg) and ¾ Nephrectomy receiving aliskiren (10 mg/kg). Urine output, water intake, mean arterial pressure (MAP) and urinary concentrations of creatinine, urea, albuminuria, Na+, K+, interleukin (IL) -1β, IL-6, IL-10 and transforming growth factor beta (TGF-β) were measured. Results: Nephrectomy significantly impaired renal function, increased MAP and altered the levels of all evaluated cytokines in urine. Enalapril, candesartan and aliskiren improved renal function and decreased MAP and IL-6 when compared to vehicle-treated nephrectomized group. Candesartan and aliskiren decreased IL-1β, while only candesartan reduced TGF-β and only aliskiren increased IL-10. Conclusion: Enalapril, candesartan and aliskiren presented similar effects on improving renal function and reducing MAP and urinary levels of IL-6 in rats with CKD. On the other hand, cytokine profile differed according to the treatment, suggesting that differential mechanisms were triggered in response to the site of RAS blockade.Sociedade Brasileira de Nefrologia2017-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000200108Brazilian Journal of Nephrology v.39 n.2 2017reponame:Jornal Brasileiro de Nefrologiainstname:Sociedade Brasileira de Nefrologia (SBN)instacron:SBN10.5935/0101-2800.20170028info:eu-repo/semantics/openAccessBaracho,Nilo César do ValeSilveira,Kátia Daniela daRocha,Natália PessoaCordeiro,Thiago MacedoFeracin,VictorPereira,Regina MariaReis,Marconi Augusto Aguiar dosTeixeira,Mauro MartinsSilva,Ana Cristina Simões eeng2017-08-15T00:00:00Zoai:scielo:S0101-28002017000200108Revistahttp://www.bjn.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||jbn@sbn.org.br2175-82390101-2800opendoar:2017-08-15T00:00Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)false
dc.title.none.fl_str_mv Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
title Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
spellingShingle Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
Baracho,Nilo César do Vale
angiotensins
angiotensin-converting enzyme inhibitors
angiotensin receptor antagonists
kidney failure, chronic
nephrectomy
title_short Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
title_full Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
title_fullStr Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
title_full_unstemmed Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
title_sort Urinary cytokine profiles according to the site of blockade of the renin-angiotensin system in nephrectomized rats
author Baracho,Nilo César do Vale
author_facet Baracho,Nilo César do Vale
Silveira,Kátia Daniela da
Rocha,Natália Pessoa
Cordeiro,Thiago Macedo
Feracin,Victor
Pereira,Regina Maria
Reis,Marconi Augusto Aguiar dos
Teixeira,Mauro Martins
Silva,Ana Cristina Simões e
author_role author
author2 Silveira,Kátia Daniela da
Rocha,Natália Pessoa
Cordeiro,Thiago Macedo
Feracin,Victor
Pereira,Regina Maria
Reis,Marconi Augusto Aguiar dos
Teixeira,Mauro Martins
Silva,Ana Cristina Simões e
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Baracho,Nilo César do Vale
Silveira,Kátia Daniela da
Rocha,Natália Pessoa
Cordeiro,Thiago Macedo
Feracin,Victor
Pereira,Regina Maria
Reis,Marconi Augusto Aguiar dos
Teixeira,Mauro Martins
Silva,Ana Cristina Simões e
dc.subject.por.fl_str_mv angiotensins
angiotensin-converting enzyme inhibitors
angiotensin receptor antagonists
kidney failure, chronic
nephrectomy
topic angiotensins
angiotensin-converting enzyme inhibitors
angiotensin receptor antagonists
kidney failure, chronic
nephrectomy
description Abstract Introduction: It is still unknown how the pharmacological inhibition of the Renin Angiotensin System (RAS) impacts the levels of inflammation and fibrosis biomarkers. Objective: This study sought to evaluate the effect of enalapril, candesartan and aliskiren on urinary levels of cytokines in a model of chronic kidney disease (CKD). Methods: Male Wistar rats were submitted to surgical removal of ¾ of renal parenchyma to induce CKD (¾ nephrectomy), or subjected to sham surgery (control). Animals were then randomized into five groups: Sham surgery receiving vehicle; ¾ Nephrectomy receiving vehicle; ¾ Nephrectomy receiving enalapril (10 mg/kg); ¾ Nephrectomy receiving candesartan (10 mg/kg) and ¾ Nephrectomy receiving aliskiren (10 mg/kg). Urine output, water intake, mean arterial pressure (MAP) and urinary concentrations of creatinine, urea, albuminuria, Na+, K+, interleukin (IL) -1β, IL-6, IL-10 and transforming growth factor beta (TGF-β) were measured. Results: Nephrectomy significantly impaired renal function, increased MAP and altered the levels of all evaluated cytokines in urine. Enalapril, candesartan and aliskiren improved renal function and decreased MAP and IL-6 when compared to vehicle-treated nephrectomized group. Candesartan and aliskiren decreased IL-1β, while only candesartan reduced TGF-β and only aliskiren increased IL-10. Conclusion: Enalapril, candesartan and aliskiren presented similar effects on improving renal function and reducing MAP and urinary levels of IL-6 in rats with CKD. On the other hand, cytokine profile differed according to the treatment, suggesting that differential mechanisms were triggered in response to the site of RAS blockade.
publishDate 2017
dc.date.none.fl_str_mv 2017-06-01
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000200108
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000200108
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0101-2800.20170028
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 Sociedade Brasileira de Nefrologia
publisher.none.fl_str_mv Sociedade Brasileira de Nefrologia
dc.source.none.fl_str_mv Brazilian Journal of Nephrology v.39 n.2 2017
reponame:Jornal Brasileiro de Nefrologia
instname:Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
instname_str Sociedade Brasileira de Nefrologia (SBN)
instacron_str SBN
institution SBN
reponame_str Jornal Brasileiro de Nefrologia
collection Jornal Brasileiro de Nefrologia
repository.name.fl_str_mv Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)
repository.mail.fl_str_mv ||jbn@sbn.org.br
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