Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/194032
Type: Artigo de periódico
Title: Effect Of Chronic Growth Hormone Treatment On Insulin Signal Transduction In Rat Tissues.
Author: Thirone, A C
Carvalho, C R
Brenelli, S L
Velloso, L A
Saad, M J
Abstract: Growth hormone (GH) is known to produce insulin resistance, but the exact molecular mechanism remains unclear. We have chronically treated rats with GH and observed that the levels of insulin receptor in the liver or muscle were similar in both the GH-treated and non-treated rats. Insulin-stimulated receptor autophosphorylation was unaltered in the liver, but was reduced in the muscle of rats treated with GH. Insulin receptor substrate-1 (IRS-1) and phosphatidylinositol (PI) 3-kinase protein levels decreased in the liver but not muscle of GH-treated rats. There was no change in hepatic and muscle IRS-2 concentrations. A common finding in liver and muscle was the decrease in IRS-1 and IRS-2 tyrosine phosphorylation associated with a reduction in the interaction between these substrates and PI 3-kinase. These data suggest that changes in the early steps of insulin signal transduction may have a role in the insulin resistance observed in rats exposed to an excess of GH.
Subject: Animals
Human Growth Hormone
Insulin
Insulin Receptor Substrate Proteins
Insulin Resistance
Intracellular Signaling Peptides And Proteins
Liver
Male
Muscle, Skeletal
Phosphatidylinositol 3-kinases
Phosphoproteins
Phosphorylation
Phosphotransferases (alcohol Group Acceptor)
Rats
Rats, Wistar
Receptor, Insulin
Signal Transduction
Rights: fechado
Identifier DOI: 
Address: http://www.ncbi.nlm.nih.gov/pubmed/9220019
Date Issue: 1997
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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