Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats

Detalhes bibliográficos
Autor(a) principal: Gil, Frida Zaladek [UNIFESP]
Data de Publicação: 2005
Outros Autores: Lucas, Sandra Regina Rodrigues [UNIFESP], Gomes, Guiomar Nascimento [UNIFESP], Cavanal, Maria de Fátima [UNIFESP], Coimbra, Terezila Machado
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/28270
http://dx.doi.org/10.1203/01.PDR.0000159514.06939.7E
Resumo: We have previously demonstrated that restricting intrauterine food by 50% in 3-mo-old rats produced lower nephron numbers and early-onset hypertension, the latter being normalized by L-arginine administration. in 18-mo-old rats, such restriction increased glomerulosclerosis. in this study, we expanded our investigation, evaluating functional, morphologic, and immunohistochemical parameters in intrauterine-food-restricted 18-mo-old rats, either receiving L-arginine (RA18) or not (R18). Age-matched, non-food-restricted controls were assigned to similar groups with L-arginine (CA18) and without (C18). After weaning, L-arginine was given daily for 17 mo. No functional or morphologic changes were observed in C IS rats. the R18 rats developed early-onset hypertension, which persisted throughout the observation period, as well its significant proteinuria from 12 mo on. in RA18 rats, L-arginine decreased both blood pressure levels and proteinuria, and glomerular diameter was si,significantly smaller than in R18 rats (115.63 +/- 2.2 versus 134.8 +/- 1.0 mu m, p < 0.05). However, in RA18 rats, glomerular filtration rate remained depressed. Although L-arginine prevented glomerulosclerosis (R18 = 14%, RA18 = 4%; p < 0.05), glomerular expression of fibronectin and desmin was still greater in RA18 rats than in controls. Our data show that, although L-arginine prevented hypertension and proteinuria, glomerular injury still occurred, suggesting that intrauterine food restriction may be one of the leading causes of impaired renal function in adult life.
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spelling Gil, Frida Zaladek [UNIFESP]Lucas, Sandra Regina Rodrigues [UNIFESP]Gomes, Guiomar Nascimento [UNIFESP]Cavanal, Maria de Fátima [UNIFESP]Coimbra, Terezila MachadoUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)2016-01-24T12:37:49Z2016-01-24T12:37:49Z2005-05-01Pediatric Research. Baltimore: Int Pediatric Research Foundation, Inc, v. 57, n. 5, p. 724-731, 2005.0031-3998http://repositorio.unifesp.br/handle/11600/28270http://dx.doi.org/10.1203/01.PDR.0000159514.06939.7E10.1203/01.PDR.0000159514.06939.7EWOS:000228645700020We have previously demonstrated that restricting intrauterine food by 50% in 3-mo-old rats produced lower nephron numbers and early-onset hypertension, the latter being normalized by L-arginine administration. in 18-mo-old rats, such restriction increased glomerulosclerosis. in this study, we expanded our investigation, evaluating functional, morphologic, and immunohistochemical parameters in intrauterine-food-restricted 18-mo-old rats, either receiving L-arginine (RA18) or not (R18). Age-matched, non-food-restricted controls were assigned to similar groups with L-arginine (CA18) and without (C18). After weaning, L-arginine was given daily for 17 mo. No functional or morphologic changes were observed in C IS rats. the R18 rats developed early-onset hypertension, which persisted throughout the observation period, as well its significant proteinuria from 12 mo on. in RA18 rats, L-arginine decreased both blood pressure levels and proteinuria, and glomerular diameter was si,significantly smaller than in R18 rats (115.63 +/- 2.2 versus 134.8 +/- 1.0 mu m, p < 0.05). However, in RA18 rats, glomerular filtration rate remained depressed. Although L-arginine prevented glomerulosclerosis (R18 = 14%, RA18 = 4%; p < 0.05), glomerular expression of fibronectin and desmin was still greater in RA18 rats than in controls. Our data show that, although L-arginine prevented hypertension and proteinuria, glomerular injury still occurred, suggesting that intrauterine food restriction may be one of the leading causes of impaired renal function in adult life.Universidade Federal de São Paulo, Dept Physiol, EPM, Dept Physiol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Physiol, EPM, Dept Morphol,Embrol Div, BR-04023900 São Paulo, BrazilUniv São Paulo, Ribeirao Preto Sch Med, Dept Physiol & Biophys, Brookline, MA 02146 USAUniversidade Federal de São Paulo, Dept Physiol, EPM, Dept Physiol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Physiol, EPM, Dept Morphol,Embrol Div, BR-04023900 São Paulo, BrazilWeb of Science724-731engInt Pediatric Research Foundation, IncPediatric ResearchEffects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of ratsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/282702023-02-15 10:56:36.706metadata only accessoai:repositorio.unifesp.br:11600/28270Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-02-15T13:56:36Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
title Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
spellingShingle Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
Gil, Frida Zaladek [UNIFESP]
title_short Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
title_full Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
title_fullStr Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
title_full_unstemmed Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
title_sort Effects of intrauterine food restriction and long-term dietary supplementation with L-arginine on age-related changes in renal function and structure of rats
author Gil, Frida Zaladek [UNIFESP]
author_facet Gil, Frida Zaladek [UNIFESP]
Lucas, Sandra Regina Rodrigues [UNIFESP]
Gomes, Guiomar Nascimento [UNIFESP]
Cavanal, Maria de Fátima [UNIFESP]
Coimbra, Terezila Machado
author_role author
author2 Lucas, Sandra Regina Rodrigues [UNIFESP]
Gomes, Guiomar Nascimento [UNIFESP]
Cavanal, Maria de Fátima [UNIFESP]
Coimbra, Terezila Machado
author2_role author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Gil, Frida Zaladek [UNIFESP]
Lucas, Sandra Regina Rodrigues [UNIFESP]
Gomes, Guiomar Nascimento [UNIFESP]
Cavanal, Maria de Fátima [UNIFESP]
Coimbra, Terezila Machado
description We have previously demonstrated that restricting intrauterine food by 50% in 3-mo-old rats produced lower nephron numbers and early-onset hypertension, the latter being normalized by L-arginine administration. in 18-mo-old rats, such restriction increased glomerulosclerosis. in this study, we expanded our investigation, evaluating functional, morphologic, and immunohistochemical parameters in intrauterine-food-restricted 18-mo-old rats, either receiving L-arginine (RA18) or not (R18). Age-matched, non-food-restricted controls were assigned to similar groups with L-arginine (CA18) and without (C18). After weaning, L-arginine was given daily for 17 mo. No functional or morphologic changes were observed in C IS rats. the R18 rats developed early-onset hypertension, which persisted throughout the observation period, as well its significant proteinuria from 12 mo on. in RA18 rats, L-arginine decreased both blood pressure levels and proteinuria, and glomerular diameter was si,significantly smaller than in R18 rats (115.63 +/- 2.2 versus 134.8 +/- 1.0 mu m, p < 0.05). However, in RA18 rats, glomerular filtration rate remained depressed. Although L-arginine prevented glomerulosclerosis (R18 = 14%, RA18 = 4%; p < 0.05), glomerular expression of fibronectin and desmin was still greater in RA18 rats than in controls. Our data show that, although L-arginine prevented hypertension and proteinuria, glomerular injury still occurred, suggesting that intrauterine food restriction may be one of the leading causes of impaired renal function in adult life.
publishDate 2005
dc.date.issued.fl_str_mv 2005-05-01
dc.date.accessioned.fl_str_mv 2016-01-24T12:37:49Z
dc.date.available.fl_str_mv 2016-01-24T12:37:49Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Pediatric Research. Baltimore: Int Pediatric Research Foundation, Inc, v. 57, n. 5, p. 724-731, 2005.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/28270
http://dx.doi.org/10.1203/01.PDR.0000159514.06939.7E
dc.identifier.issn.none.fl_str_mv 0031-3998
dc.identifier.doi.none.fl_str_mv 10.1203/01.PDR.0000159514.06939.7E
dc.identifier.wos.none.fl_str_mv WOS:000228645700020
identifier_str_mv Pediatric Research. Baltimore: Int Pediatric Research Foundation, Inc, v. 57, n. 5, p. 724-731, 2005.
0031-3998
10.1203/01.PDR.0000159514.06939.7E
WOS:000228645700020
url http://repositorio.unifesp.br/handle/11600/28270
http://dx.doi.org/10.1203/01.PDR.0000159514.06939.7E
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Pediatric Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 724-731
dc.publisher.none.fl_str_mv Int Pediatric Research Foundation, Inc
publisher.none.fl_str_mv Int Pediatric Research Foundation, Inc
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
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