The regulatory role of skeleton in maintaining glucose homeostasis
10.3760/cma.j.issn.1000-6699.2016.12.008
- VernacularTitle:骨骼对维持血糖稳态的作用
- Author:
Dongmei LIU
;
Jianmin LIU
;
Mingdao CHEN
- Keywords:
Skeleton;
Osteoblast;
Osteocalcin;
Diabetes;
Glucose metabolism
- From:
Chinese Journal of Endocrinology and Metabolism
2016;32(12):1015-1022
- CountryChina
- Language:Chinese
-
Abstract:
Bone is now regarded as an endocrine organ modulating energy metabolism. Osteocalcin, which was a traditional bone remodeling marker, especially in its undercarboxylated form, was believed to be a metabolic active molecule involving in glucose homeostasis. Bone can uptake glucose through glucose transporter 1 expressed on osteoblasts, and this process is crucial for osteoblasts differentiation and bone formation. In addition, the osteoblasts specific insulin resistance may also lead to the dysregulation of whole body glucose metabolism. Clinical investigations generally echo the findings from mice studies. More work, especially prospective clinical studies are needed to prove the clinical utility of osteocalcin and/or other bone turnover parameters as solid predictors of pancreaticβcell function and incident diabetes, as well as the potential use of osteocalcin and/or its undercarboxylated form as an anti-diabetic agent. In the 11th issue of Diabetes in 2016, a review paper entitled asRegulation of glucose handling by the skeleton:Insights from mouse and human studies was published [Diabetes, 2016,65(11):3225-3232]. With the permission of Diabetes and American Diabetes Association, we translated the most important part of this review into Chinese with a new title:The regulatory role of skeleton in maintaining glucose homeostasis.
