Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers

Detalhes bibliográficos
Autor(a) principal: Correa-Costa, Matheus
Data de Publicação: 2012
Outros Autores: Landgraf, Maristella A., Cavanal, Maria de Fátima [UNIFESP], Semedo, Patricia [UNIFESP], Vieira, Daniel Augusto Ghiraldini [UNIFESP], Marco, Davi Tjhio Kolar de [UNIFESP], Hirata, Aparecida Emiko [UNIFESP], Câmara, Niels Olsen Saraiva [UNIFESP], Gil, Frida Zaladek [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.ejphar.2012.05.024
http://repositorio.unifesp.br/handle/11600/35175
Resumo: The present study investigated the early presence of inflammatory response in renal tissue of young offspring from diabetic mothers. the effect of L-arginine (L-arg) supplementation was also investigated. the offspring was divided into four groups: group CO (controls); group DO (diabetic offspring); group CA (CO receiving 2% L-arg solution) and group DA (DO receiving the 2% L-arg solution). Glycemia, arterial pressure and renal function were evaluated; gene and protein expression of pro-inflammatory cytokines were also measured. Blood pressure levels were significantly increased in 2 and 6 month-old DO rats, whereas L-arg administration caused a significant decrease in the DA group, at both ages. DO rats showed a significantly blunted glycemic response to exogenous insulin. in 2 month-old DO animals, renal protein expression of pro-inflammatory molecules was significantly increased. At six months of age, we also observed an increase in gene expression of pro-inflammatory molecules, whereas L-arg supplementation prevented this increase at both ages. Our data suggest that activation of inflammatory pathways is present early in the kidney of DO rats, and that L-arg can attenuate the expression of these markers of tissue inflammation. Our results also reinforce the concept that intrauterine environmental factors are a fundamental determinant in the development of metabolic and vascular diseases later in life. (C) 2012 Elsevier B.V. All rights reserved.
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spelling Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothersFetal programmingMaternal diabetesRenal inflammationL-arginineThe present study investigated the early presence of inflammatory response in renal tissue of young offspring from diabetic mothers. the effect of L-arginine (L-arg) supplementation was also investigated. the offspring was divided into four groups: group CO (controls); group DO (diabetic offspring); group CA (CO receiving 2% L-arg solution) and group DA (DO receiving the 2% L-arg solution). Glycemia, arterial pressure and renal function were evaluated; gene and protein expression of pro-inflammatory cytokines were also measured. Blood pressure levels were significantly increased in 2 and 6 month-old DO rats, whereas L-arg administration caused a significant decrease in the DA group, at both ages. DO rats showed a significantly blunted glycemic response to exogenous insulin. in 2 month-old DO animals, renal protein expression of pro-inflammatory molecules was significantly increased. At six months of age, we also observed an increase in gene expression of pro-inflammatory molecules, whereas L-arg supplementation prevented this increase at both ages. Our data suggest that activation of inflammatory pathways is present early in the kidney of DO rats, and that L-arg can attenuate the expression of these markers of tissue inflammation. Our results also reinforce the concept that intrauterine environmental factors are a fundamental determinant in the development of metabolic and vascular diseases later in life. (C) 2012 Elsevier B.V. All rights reserved.Univ São Paulo, Inst Biomed Sci 4, Dept Immunol, Lab Transplantat Immunobiol, BR-05508000 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Physiol, BR-04039000 São Paulo, BrazilFed Univ São Paulo UNIFESP, Div Nephrol, BR-04039001 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Physiol, BR-04039000 São Paulo, BrazilFed Univ São Paulo UNIFESP, Div Nephrol, BR-04039001 São Paulo, BrazilWeb of ScienceFundacao de Amparo a Pesquisa do Estado de So PauloConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Instituto Nacional de Ciencia e Tecnologia de Fluidos Complexos (INCT Complex Fluids)Fundacao de Amparo a Pesquisa do Estado de So Paulo: 2007/07139-3Fundacao de Amparo a Pesquisa do Estado de So Paulo: 2010/17782-3Fundacao de Amparo a Pesquisa do Estado de So Paulo: 2012/02270-2Fundacao de Amparo a Pesquisa do Estado de So Paulo: 2010/52180-4Elsevier B.V.Universidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Correa-Costa, MatheusLandgraf, Maristella A.Cavanal, Maria de Fátima [UNIFESP]Semedo, Patricia [UNIFESP]Vieira, Daniel Augusto Ghiraldini [UNIFESP]Marco, Davi Tjhio Kolar de [UNIFESP]Hirata, Aparecida Emiko [UNIFESP]Câmara, Niels Olsen Saraiva [UNIFESP]Gil, Frida Zaladek [UNIFESP]2016-01-24T14:27:34Z2016-01-24T14:27:34Z2012-08-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion233-240application/pdfhttp://dx.doi.org/10.1016/j.ejphar.2012.05.024European Journal of Pharmacology. Amsterdam: Elsevier B.V., v. 689, n. 1-3, p. 233-240, 2012.10.1016/j.ejphar.2012.05.024WOS000306646900032.pdf0014-2999http://repositorio.unifesp.br/handle/11600/35175WOS:000306646900032engEuropean Journal of Pharmacologyinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T02:18:45Zoai:repositorio.unifesp.br/:11600/35175Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-01T02:18:45Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
title Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
spellingShingle Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
Correa-Costa, Matheus
Fetal programming
Maternal diabetes
Renal inflammation
L-arginine
title_short Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
title_full Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
title_fullStr Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
title_full_unstemmed Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
title_sort Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
author Correa-Costa, Matheus
author_facet Correa-Costa, Matheus
Landgraf, Maristella A.
Cavanal, Maria de Fátima [UNIFESP]
Semedo, Patricia [UNIFESP]
Vieira, Daniel Augusto Ghiraldini [UNIFESP]
Marco, Davi Tjhio Kolar de [UNIFESP]
Hirata, Aparecida Emiko [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
Gil, Frida Zaladek [UNIFESP]
author_role author
author2 Landgraf, Maristella A.
Cavanal, Maria de Fátima [UNIFESP]
Semedo, Patricia [UNIFESP]
Vieira, Daniel Augusto Ghiraldini [UNIFESP]
Marco, Davi Tjhio Kolar de [UNIFESP]
Hirata, Aparecida Emiko [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
Gil, Frida Zaladek [UNIFESP]
author2_role author
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 Correa-Costa, Matheus
Landgraf, Maristella A.
Cavanal, Maria de Fátima [UNIFESP]
Semedo, Patricia [UNIFESP]
Vieira, Daniel Augusto Ghiraldini [UNIFESP]
Marco, Davi Tjhio Kolar de [UNIFESP]
Hirata, Aparecida Emiko [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
Gil, Frida Zaladek [UNIFESP]
dc.subject.por.fl_str_mv Fetal programming
Maternal diabetes
Renal inflammation
L-arginine
topic Fetal programming
Maternal diabetes
Renal inflammation
L-arginine
description The present study investigated the early presence of inflammatory response in renal tissue of young offspring from diabetic mothers. the effect of L-arginine (L-arg) supplementation was also investigated. the offspring was divided into four groups: group CO (controls); group DO (diabetic offspring); group CA (CO receiving 2% L-arg solution) and group DA (DO receiving the 2% L-arg solution). Glycemia, arterial pressure and renal function were evaluated; gene and protein expression of pro-inflammatory cytokines were also measured. Blood pressure levels were significantly increased in 2 and 6 month-old DO rats, whereas L-arg administration caused a significant decrease in the DA group, at both ages. DO rats showed a significantly blunted glycemic response to exogenous insulin. in 2 month-old DO animals, renal protein expression of pro-inflammatory molecules was significantly increased. At six months of age, we also observed an increase in gene expression of pro-inflammatory molecules, whereas L-arg supplementation prevented this increase at both ages. Our data suggest that activation of inflammatory pathways is present early in the kidney of DO rats, and that L-arg can attenuate the expression of these markers of tissue inflammation. Our results also reinforce the concept that intrauterine environmental factors are a fundamental determinant in the development of metabolic and vascular diseases later in life. (C) 2012 Elsevier B.V. All rights reserved.
publishDate 2012
dc.date.none.fl_str_mv 2012-08-15
2016-01-24T14:27:34Z
2016-01-24T14:27:34Z
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/10.1016/j.ejphar.2012.05.024
European Journal of Pharmacology. Amsterdam: Elsevier B.V., v. 689, n. 1-3, p. 233-240, 2012.
10.1016/j.ejphar.2012.05.024
WOS000306646900032.pdf
0014-2999
http://repositorio.unifesp.br/handle/11600/35175
WOS:000306646900032
url http://dx.doi.org/10.1016/j.ejphar.2012.05.024
http://repositorio.unifesp.br/handle/11600/35175
identifier_str_mv European Journal of Pharmacology. Amsterdam: Elsevier B.V., v. 689, n. 1-3, p. 233-240, 2012.
10.1016/j.ejphar.2012.05.024
WOS000306646900032.pdf
0014-2999
WOS:000306646900032
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv European Journal of Pharmacology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.format.none.fl_str_mv 233-240
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
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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