Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid

Chronic administration of glucocorticoids induces insulin resistance that is compensated by an increase in p-cell function and mass. Since insulin signaling is involved in the control of p-cell function and mass, we investigated the content of insulin pathway proteins in pancreatic islets. Rats were...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: De Paula,Flávia MM, Boschero,Antonio C, Carneiro,Everardo M, Bosqueiro,José R, Rafacho,Alex
Lenguaje:English
Publicado: Sociedad de Biología de Chile 2011
Materias:
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602011000300006
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:scielo:S0716-97602011000300006
record_format dspace
spelling oai:scielo:S0716-976020110003000062011-11-07Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoidDe Paula,Flávia MMBoschero,Antonio CCarneiro,Everardo MBosqueiro,José RRafacho,Alex dexamethasone glucocorticoid insulin resistance insulin signaling pancreatic islets Chronic administration of glucocorticoids induces insulin resistance that is compensated by an increase in p-cell function and mass. Since insulin signaling is involved in the control of p-cell function and mass, we investigated the content of insulin pathway proteins in pancreatic islets. Rats were made insulin resistant by daily administration of dexamethasone (1mg/kg, b.w., i.p.) for 5 consecutive days (DEX), whilst control rats received saline (CTL). Circulating insulin and insulin released from isolated islets were measured by radioimmunoassay whereas the content of proteins was analyzed by Western blotting. DEX rats were hyperinsulinemic and exhibited augmented insulin secretion in response to glucose (P < 0.01). The IRa-subunit, IRS-1, Shc, AKT, p-p70S6K, ERK1/2, p-ERK1/2, and glucocorticoid receptor protein levels were similar between DEX and CTL islets. However, the IRp-subunit, p-IRp-subunit, IRS-2, PI3-K, p-AKT and p70S6K protein contents were increased in DEX islets (P < 0.05). We conclude that IRS-2 may have a major role, among the immediate substrates of the insulin receptor, to link activated receptors to downstream signaling components related to islet function and growth in this insulin-resistant rat model.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.44 n.3 20112011-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602011000300006en10.4067/S0716-97602011000300006
institution Scielo Chile
collection Scielo Chile
language English
topic dexamethasone
glucocorticoid
insulin resistance
insulin signaling
pancreatic islets
spellingShingle dexamethasone
glucocorticoid
insulin resistance
insulin signaling
pancreatic islets
De Paula,Flávia MM
Boschero,Antonio C
Carneiro,Everardo M
Bosqueiro,José R
Rafacho,Alex
Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
description Chronic administration of glucocorticoids induces insulin resistance that is compensated by an increase in p-cell function and mass. Since insulin signaling is involved in the control of p-cell function and mass, we investigated the content of insulin pathway proteins in pancreatic islets. Rats were made insulin resistant by daily administration of dexamethasone (1mg/kg, b.w., i.p.) for 5 consecutive days (DEX), whilst control rats received saline (CTL). Circulating insulin and insulin released from isolated islets were measured by radioimmunoassay whereas the content of proteins was analyzed by Western blotting. DEX rats were hyperinsulinemic and exhibited augmented insulin secretion in response to glucose (P < 0.01). The IRa-subunit, IRS-1, Shc, AKT, p-p70S6K, ERK1/2, p-ERK1/2, and glucocorticoid receptor protein levels were similar between DEX and CTL islets. However, the IRp-subunit, p-IRp-subunit, IRS-2, PI3-K, p-AKT and p70S6K protein contents were increased in DEX islets (P < 0.05). We conclude that IRS-2 may have a major role, among the immediate substrates of the insulin receptor, to link activated receptors to downstream signaling components related to islet function and growth in this insulin-resistant rat model.
author De Paula,Flávia MM
Boschero,Antonio C
Carneiro,Everardo M
Bosqueiro,José R
Rafacho,Alex
author_facet De Paula,Flávia MM
Boschero,Antonio C
Carneiro,Everardo M
Bosqueiro,José R
Rafacho,Alex
author_sort De Paula,Flávia MM
title Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
title_short Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
title_full Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
title_fullStr Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
title_full_unstemmed Insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
title_sort insulin signaling proteins in pancreatic islets of insulin-resistant rats induced by glucocorticoid
publisher Sociedad de Biología de Chile
publishDate 2011
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602011000300006
work_keys_str_mv AT depaulaflaviamm insulinsignalingproteinsinpancreaticisletsofinsulinresistantratsinducedbyglucocorticoid
AT boscheroantonioc insulinsignalingproteinsinpancreaticisletsofinsulinresistantratsinducedbyglucocorticoid
AT carneiroeverardom insulinsignalingproteinsinpancreaticisletsofinsulinresistantratsinducedbyglucocorticoid
AT bosqueirojoser insulinsignalingproteinsinpancreaticisletsofinsulinresistantratsinducedbyglucocorticoid
AT rafachoalex insulinsignalingproteinsinpancreaticisletsofinsulinresistantratsinducedbyglucocorticoid
_version_ 1718441477761138688