Article ID Journal Published Year Pages File Type
1925536 Archives of Biochemistry and Biophysics 2012 8 Pages PDF
Abstract

Vitamin D was discovered as an anti-rachitic agent, but even at present, there is no direct evidence to support the concept that vitamin D directly stimulates osteoblastic bone formation and mineralization. It appears to be paradoxical, but vitamin D functions in the process of osteoclastic bone resorption. In 1952, Carlsson reported that administration of vitamin D3 to rats fed a vitamin D-deficient, low calcium diet raised serum calcium levels. Since the diet did not contain appreciable amounts of calcium, the rise in serum calcium was considered to be derived from bone. Since then, this assay has been used as a standard bioassay for vitamin D compounds. Osteoclasts, the cells responsible for bone resorption, develop from hematopoietic cells of the monocyte-macrophage lineage. Several lines of evidence have shown that the active form of vitamin D3, 1α,25-dihydroxyvitamin D3 [1α,25(OH)2D3] is one of the most potent inducers of receptor activator of NF-κB ligand (RANKL), a key molecule for osteoclastogenesis, in vitro. In fact, 1α,25(OH)2D3 strongly induced osteoclast formation and bone resorption in vitro. Nevertheless, 1α,25(OH)2D3 and its prodrug, Alfacalcidol (1α-hydroxyvitamin D3) have been used as therapeutic agents for osteoporosis since 1983, because they increase bone mineral density and reduce the incidence of bone fracture in vivo. Furthermore, a new vitamin D analog, Eldecalcitol [2β-(3-hydroxypropoxy)-1α,25(OH)2D3], has been approved as a new drug for osteoporosis in Japan in January 2011. Interestingly, these beneficial effects of in vivo administration of vitamin D compounds are caused by the suppression of osteoclastic bone resorption. The present review article describes the mechanism of the discrepancy of vitamin D compounds in osteoclastic bone resorption between in vivo and in vitro.

► Active forms of vitamin D have been used as therapeutic agents for osteoporosis. ► Active vitamin D compounds, however, stimulate osteoclastogenesis in vitro. ► Daily administration of vitamin D compounds reversely inhibits bone resorption in vivo. ► Discrepancy of bone effects of vitamin D between in vivo and in vitro is discussed. ► Characterization of a new active vitamin D analog (Eldecalcitol) is also described.

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