Loss of mPer2 increases plasma insulin levels by enhanced glucose-stimulated insulin secretion and impaired insulin clearance in mice

被引:48
作者
Zhao, Yue [1 ]
Zhang, Ying [1 ]
Zhou, Mengyi [1 ]
Wang, Shiming [1 ]
Hua, Zichun [2 ]
Zhang, Jianfa [1 ,2 ]
机构
[1] Nanjing Univ Sci & Technol, Ctr Mol Metab, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Nanjing, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
mPer2; Insulin secretion; Insulin clearance; Glucose homeostasis; CIRCADIAN CLOCK; LIPID-METABOLISM; DEGRADING ENZYME; GENE PER2; IN-VIVO; HYPERINSULINEMIA; EXPRESSION; MUTATION; PROTEIN; MOUSE;
D O I
10.1016/j.febslet.2012.03.034
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 existence of peripheral oscillators has been shown, and they are critically important for organizing the metabolism of the whole body. Here we show that mice deficient in mPer2 markedly increase circulatory levels of insulin compared with wild type mice. Insulin secretion was more effectively stimulated by glucose, and alloxan, a glucose analogue, induced more severe hyperglycemia in mPer2-deficient mice. Hepatic insulin degrading enzyme (Ide) displayed an obvious day and night rhythm, which was impaired in mPer2-deficient mice, leading to a decrease in insulin clearance. Deficiency in mPer2 caused increased Clock expression and decreased expression of Mkp1 and Ide1, possibly underlying the observed phenotypes and suggesting that mPer2 plays a role in regulation of circulating insulin levels. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1306 / 1311
页数:6
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