Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19252
Title: Sex-related differences in the skeletal phenotype of aged vitamin D receptor global knockout mice.
Austin Authors: Ryan, Jackson W;Starczak, Yolandi;Tsangari, Helen;Sawyer, Rebecca K;Davey, Rachel A;Atkins, Gerald J;Morris, Howard A;Anderson, Paul H
Affiliation: School of Pharmacy and Medical Sciences, Sansom Institute, University of South Australia, Adelaide, SA 5001, Australia
Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Centre for Orthopaedic and Trauma Research, School of Medicine, University of Adelaide, Adelaide, SA 5001, Australia
Issue Date: Nov-2016
metadata.dc.date: 2015-12-09
Publication information: The Journal of steroid biochemistry and molecular biology 2016; 164: 361-368
Abstract: The role of the vitamin D receptor (VDR) in maintaining skeletal health appears to be complex and dependent on the physiological context. Global Vdr deletion in a mouse model (Vdr-/-) results in hypocalcemia, secondary hyperparathyroidism and bone features typical of vitamin D-dependent rickets type II. When weanling Vdr-/- mice are fed a diet containing high levels of calcium, phosphorus and lactose, termed the rescue diet, normalisation of serum calcium, phosphate and parathyroid hormone levels results in prevention of rickets at 10 weeks of age. However, 17 week old male Vdr-/- mice, fed the rescue diet, have been reported as osteopenic due to a decrease in bone formation when compared to wild type mice. We now report confirmation of this finding with further data on the effect of the rescue diet on appendicular and axial skeletal structures in male and female Vdr-/- mice at 26 weeks of age compared to Vdr+/- controls. All Vdr-/- mice were normocalcemic with no evidence of any mineralization defect. However, male Vdr-/- mice exhibited significantly reduced mineral in femoral and vertebral bones when compared to control littermate Vdr+/- mice, consistent with the previously reported data. In contrast, 26-week-old female Vdr-/- mice demonstrated significantly increased femoral trabecular bone volume although there was decreased vertebral trabecular bone volume, similar to males, and femoral cortical bone volume was unchanged. Thus, the Vdr-/- mouse model displays sex- and site-specific differences in skeletal structures with long-term feeding of a rescue diet. Although the global Vdr-/- ablation does not permit the determination of skeletal mechanisms producing these differences, these data confirm skeletal changes even when fed the rescue diet.
URI: http://ahro.austin.org.au/austinjspui/handle/1/19252
DOI: 10.1016/j.jsbmb.2015.12.005
ORCID: 0000-0001-5121-0209
PubMed URL: 26690785
Type: Journal Article
Subjects: 1,25-Dihydroxyvitamin D(3)
Bone remodelling
Osteoblasts
Osteoclasts
Vitamin D receptor
Appears in Collections:Journal articles

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