Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/117528
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Type: Journal article
Title: Short-term hypoxia accelerates bone loss in ovariectomized rats by suppressing osteoblastogenesis but enhancing osteoclastogenesis
Author: Wang, G.
Wang, J.
Sun, D.
Xin, J.
Wang, L.
Huang, D.
Wu, W.
Xian, C.J.
Citation: Medical Science Monitor: international medical journal for clinical and experimental research, 2016; 22:2961-2971
Publisher: Medical Science International Publishing
Issue Date: 2016
ISSN: 1234-1010
1643-3750
Statement of
Responsibility: 
Guixin Wang, Jia Wang, Dawei Sun, Jingyi Xin, Liping Wang, Dong Huang, Weichi Wu, Cory J. Xian
Abstract: BACKGROUND: Although it has been reported that hypoxic exposure can attenuate hypertension, heart disease, diabetes, and some other diseases, effects of hypoxia on osteoporosis are still unknown. MATERIAL AND METHODS: The current study investigated whether short-term hypoxic exposure (in comparison with normoxic conditions) affects bone metabolism in normal or ovariectomized (OVX) adult female rats in an vivo study. Micro-computed tomography bone volume/structural analyses, histological examination, and serum bone turnover biochemical assays were used. In addition, the expressions of some associated major regulatory molecules were measured in osteoblastic cultures. RESULTS: While the 14-day hypoxic exposure did not change the bone-remodeling process in normal adult female rats, it decreased bone volume, osteoclast density, and serum bone formation marker (alkaline phosphatase) level, but increased osteoclast density and serum bone resorption marker (C-telopeptide of collagen) level in OVX rats. The bone marrow adipocyte number and serum fatty acid binding protein-4 level were increased in OVX-hypoxic rats compared with OVX-normoxic rats. Consistently, in human MG-63 osteoblastic cultures, the hypoxic condition suppressed protein expression of osteogenic transcriptional factors Runx2 and osterix, elevated protein expression of osteoclastogenic cytokine receptor activator of nuclear factor kappa-B ligand, but reduced that of osteoclastogenic inhibitor osteoprotegerin. CONCLUSIONS: Our results suggest that, although no change occurred in the bone-remodeling process in normal adult female rats after hypoxic exposure, under the estrogen-deficient osteoporotic condition, the hypoxic condition can alter the bone microenvironment so that it may further impair osteoblastic differentiation and enhance osteoclastic formation, and thus reduce bone formation, enhance bone resorption, and accelerate bone loss.
Keywords: Cell dedifferentiation; cell hypoxia; osteoblasts; osteoclasts; osteoporosis
Rights: © Med Sci Monit, 2016. This work is licensed under Creative Common Attribution- NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
DOI: 10.12659/MSM.899485
Grant ID: NHMRC
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