Resistin induces insulin resistance in pancreatic islets to impair glucose-induced insulin release

被引:62
作者
Nakata, Masanori [1 ]
Okada, Takashi
Ozawa, Keiya
Yada, Toshihiko
机构
[1] Jichi Med Univ, Dept Physiol, Div Integrat Physiol, Sch Med, Shimotsuke, Tochigi 3290498, Japan
[2] Jichi Med Univ, Ctr Mol Med, Div Genet Therapeut, Sch Med, Shimotsuke, Tochigi 3290498, Japan
基金
日本学术振兴会;
关键词
insulin; resistin; pancreatic beta-cell; obesity; adipokine;
D O I
10.1016/j.bbrc.2006.12.134
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
An adipokine resistin, a small cysteine-rich protein, is one of the major risk factors of insulin resistance. In the present study, transiently resistin-expressing mice using adenovirus method showed an impaired glucose tolerance due to insulin resistance. We found that resistin-expressing mice exhibited impaired insulin secretory response to glucose. In addition, in vitro treatment with resistin for I day induced insulin resistance in pancreatic islets and impaired glucose-stimulated insulin secretion by elevating insulin release at basal glucose (2.8 mM) and suppressing insulin release at stimulatory glucose (8.3 mM). In addition, resistin inhibited insulin-induced phosphorylation of Akt in islets as well as other insulin target organs. Furthermore, resistin induced SOCS-3 expression in P-cells. In conclusion, resistin induces insulin resistance in islet beta-cells at least partly via induction of SOCS-3 expression and reduction of Akt phosphorylation and impairs glucose-induced insulin secretion. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1046 / 1051
页数:6
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