Literature DB >> 21550430

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

Mathieu Ferron1, Marc D McKee, Robert L Levine, Patricia Ducy, Gérard Karsenty.   

Abstract

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 β-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.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21550430      PMCID: PMC3181267          DOI: 10.1016/j.bone.2011.04.017

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  30 in total

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3.  The effects of variations in dose and method of administration on glucagon like peptide-2 activity in the rat.

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Journal:  Eur J Pharmacol       Date:  2008-08-22       Impact factor: 4.432

4.  Association between serum osteocalcin and markers of metabolic phenotype.

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Journal:  J Clin Endocrinol Metab       Date:  2008-12-16       Impact factor: 5.958

5.  Osteocalcin differentially regulates beta cell and adipocyte gene expression and affects the development of metabolic diseases in wild-type mice.

Authors:  Mathieu Ferron; Eiichi Hinoi; Gerard Karsenty; Patricia Ducy
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  139 in total

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Review 3.  An overview of osteocalcin progress.

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4.  Increased Gs Signaling in Osteoblasts Reduces Bone Marrow and Whole-Body Adiposity in Male Mice.

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Review 5.  Insulin and bone: Recent developments.

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Journal:  Mol Metab       Date:  2013-08-15       Impact factor: 7.422

7.  Osteoblasts mediate the adverse effects of glucocorticoids on fuel metabolism.

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8.  Osteocalcin, under-carboxylated osteocalcin and osteopontin are not associated with gestational diabetes mellitus but are inversely associated with leptin in non-diabetic women.

Authors:  R Saucedo; G Rico; G Vega; L Basurto; L Cordova; R Galvan; M Hernandez; E Puello; A Zarate
Journal:  J Endocrinol Invest       Date:  2014-12-06       Impact factor: 4.256

9.  Recombinant Mouse Osteocalcin Secreted by Lactococcus lactis Promotes Glucagon-Like Peptide-1 Induction in STC-1 Cells.

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10.  Tactile/kinesthetic stimulation (TKS) increases tibial speed of sound and urinary osteocalcin (U-MidOC and unOC) in premature infants (29-32weeks PMA).

Authors:  S Haley; J Beachy; K K Ivaska; H Slater; S Smith; L J Moyer-Mileur
Journal:  Bone       Date:  2012-07-27       Impact factor: 4.398

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