Intermittent injections of osteocalcin improve glucose metabolism and prevent type 2 diabetes in mice

被引:372
作者
Ferron, Mathieu [1 ]
McKee, Marc D. [2 ,3 ]
Levine, Robert L. [1 ]
Ducy, Patricia [4 ]
Karsenty, Gerard [1 ]
机构
[1] Columbia Univ, Dept Genet & Dev, Coll Phys & Surg, New York, NY 10032 USA
[2] McGill Univ, Fac Dent, Montreal, PQ H3A 2B2, Canada
[3] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 2B2, Canada
[4] Columbia Univ, Dept Pathol & Cell Biol, Coll Phys & Surg, New York, NY 10032 USA
基金
加拿大健康研究院;
关键词
Glucose; Insulin; Osteocalcin; Energy expenditure; Liver steatosis; SERUM OSTEOCALCIN; PLASMA-GLUCOSE; FAT MASS; INSULIN; DEFICIENCY; DISEASE;
D O I
10.1016/j.bone.2011.04.017
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The uncarboxylated form of the osteoblast-specific secreted molecule osteocalcin is a hormone favoring glucose handling and increasing energy expenditure. As a result, the absence of osteocalcin leads to glucose intolerance in mice, while genetically modified mice with an increase in uncarboxylated osteocalcin are protected from type 2 diabetes and obesity. Here, we tested in the mouse the therapeutic potential of intermittent administration of osteocalcin. We found that daily injections of osteocalcin at either 3 or 30 ng/g/day significantly improved glucose tolerance and insulin sensitivity in mice fed a normal diet. This was attributable, in part, to an increase in both beta-cell mass and insulin secretion. When mice were fed a high-fat diet (HFD), daily injections of osteocalcin partially restored insulin sensitivity and glucose tolerance. Moreover, mice treated with intermittent osteocalcin injections displayed additional mitochondria in their skeletal muscle, had increased energy expenditure and were protected from diet-induced obesity. Finally, the hepatic steatosis induced by the HFD was completely rescued in mice receiving osteocalcin daily. Overall, these results provide evidence that daily injections of osteocalcin can improve glucose handling and prevent the development of type 2 diabetes. This article is part of a Special Issue entitled: Interactions Between Bone, Adipose Tissue and Metabolism. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:568 / 575
页数:8
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