Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
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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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 |
_version_ |
1814268423142637568 |