Dehydroepiandrosterone increases β-cell mass and improves the glucose-induced insulin secretion by pancreatic islets from aged rats

被引:25
|
作者
Medina, MC
Souza, LC
Caperuto, LC
Anhêh, GF
Amanso, AM
Teixeira, VPA
Bordin, S
Carpinelli, AR
Britto, LRG
Barbieri, RL
Borella, MI
Carvalho, CRO [1 ]
机构
[1] Univ Sao Paulo, ICB, Dept Physiol & Biophys, BR-05389970 Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Dev & Cell Biol, Sao Paulo, Brazil
[3] Coll Med Triangulo Mineiro, Dept Gen Pathol, Uberaba, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
DHEA; insulin secretion; aged rats; Akt; IRS proteins; pancreatic islet;
D O I
10.1016/j.febslet.2005.12.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of dehydroepiandrosterone (DHEA) on pancreatic islet function of aged rats, an animal model with impaired glucose-induced insulin secretion, was investigated. The following parameters were examined: morphological analysis of endocrine pancreata by immunohistochemistry; protein levels of insulin receptor, IRS-1, IRS-2, PI 3-kinase, Akt-1, and Akt-2; and static insulin secretion in isolated pancreatic islets. Pancreatic islets from DHEA-treated rats showed an increased beta-cell mass accompanied by increased Akt-1 protein level but reduced IR, IRS-1, and IRS-2 protein levels and enhanced glucose-stimulated insulin secretion. The present results suggest that DHEA may be a promising drug to prevent diabetes during aging. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:285 / 290
页数:6
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