Assessment of the Expression of IR beta, IRS-1, IRS-2 and IGF-IR beta in a Rat Model of Intrauterine Growth Restriction


Autoria(s): BUENO, Marcia Pereira; GUADAGNINI, Dioze; GONCALVES, Frances Lilian Lanhellas; BARINI, Ricardo; SAAD, Mario Jose Abdalla; SCHMIDT, Augusto Frederico; SBRAGIA, Lourenco
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Objective: To investigate glomerular development and expression of insulin and insulin-like growth factor receptors in an experimental model of intrauterine growth restriction (IUGR). Material and Methods: We studied three groups of Sprague-Dawley fetuses: IUGR - restricted by ligation of the right uterine artery; C-IUGR - left horn controls, and EC - external controls (non-manipulated). Body and organs were weighed, and glomerular number and volume were analyzed. Expression of IR beta, IRS-1, IRS-2 and IGF-IR beta was analyzed in liver, intestine and kidneys by immunoblotting. Results: Organ/body weight ratios were similar. In IUGR, glomerular number and volume were increased compared to C-IUGR and EC (p < 0.001). In the IUGR liver, increases were found in IGF-IR beta compared to C-IUGR and EC; IR beta compared to EC, and IRS-2 compared to C-IUGR. However, decreases in IR beta were noted in IUGR compared to C-IUGR; IRS-1 compared to C-IUGR and EC, and IRS-2 compared to EC. In IUGR intestine, increases were detected in IR beta, IRS-1 and IGF-IR beta compared to C-IUGR and EC. In IUGR kidneys, increases were observed in IR beta and IGF-IR beta compared to C-IUGR and EC, and IRS-1 compared to EC. Decreased IRS-2 in the intestine and kidney were noticed in IUGR compared to C-IUGR and EC. Conclusion: IUGR fetuses had less glomeruli and alterations in insulin receptors, which may be associated with an increased risk of disease occurrence in adulthood. Copyright (C) 2010 S. Karger AG, Basel

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo - Sao Paulo Research Foundation)[08/51487-9]

Identificador

FETAL DIAGNOSIS AND THERAPY, v.28, n.3, p.145-152, 2010

1015-3837

http://producao.usp.br/handle/BDPI/23879

10.1159/000316932

http://dx.doi.org/10.1159/000316932

Idioma(s)

eng

Publicador

KARGER

Relação

Fetal Diagnosis and Therapy

Direitos

closedAccess

Copyright KARGER

Palavras-Chave #Fetal glomerular development #Glomeruli #Insulin receptor #Insulin-like growth factor receptor #Intrauterine growth restriction #INSULIN-RESISTANCE #FETAL-GROWTH #POSTNATAL-GROWTH #ADULT DISEASE #RETARDATION #RECEPTOR #PROTEINS #HORMONE #GENE #MICE #Obstetrics & Gynecology
Tipo

article

original article

publishedVersion