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      The effect of the alendronate on OPG/RANKL system in differentiated primary human osteoblasts.

      Endocrine
      Alendronate, pharmacology, Alkaline Phosphatase, metabolism, Bone Density Conservation Agents, Cell Differentiation, drug effects, Cell Survival, Cells, Cultured, Dose-Response Relationship, Drug, Enzyme Activation, Gene Expression, Humans, Osteoblasts, cytology, physiology, Osteoprotegerin, genetics, RANK Ligand, RNA, Messenger, Vitamin D

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          Abstract

          Alendronate is a well-established treatment for osteoporosis and suppresses bone resorption by a direct effect on osteoclasts and their precursors. The effect of alendronate on osteoclasts is produced, at least in part, by the receptor activator of nuclear factor kappaB ligand (RANKL) and the osteoprotegerin (OPG) synthesized by the osteoblasts. This study analyzes the effect of alendronate in cell viability, alkaline phosphatase (ALP) activity and RANKL and OPG expression in primary human osteoblasts (hOB). Alendronate at concentrations lower than 10⁻⁵ M did not have a toxic effect on hOB in vitro and did not modify the ALP activity at least for 72 h. Alendronate did not change OPG expression in basal, 10% fetal bovine serum (FBS), and vitamin D-treated cultures. Similar results were observed at the protein level. Unexpectedly, alendronate at 10⁻⁷ and 10⁻⁵ M concentrations increased the RANKL expression with the presence of vitamin D in differentiated hOB, and this induction of RANKL mRNA levels by alendronate was dose-dependent. However, this effect was not observed in basal and 10% FBS culture conditions. Thus, we conclude that alendronate does not affect the ALP activity and OPG gene expression in differentiated hOB, but may increase RANKL gene expression induced by vitamin D.

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