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|Title:||Long-term effects of neridronate on human osteoblastic cell cultures||Authors:||Frediani, Bruno
|Keywords:||Bisphosphonates; Bone markers; Neridronate; Osteoblasts; Osteoporosis treatment; Aged; Alkaline Phosphatase; Calcification, Physiologic; Cell Differentiation; Cell Proliferation; Cells, Cultured; Collagen Type I; Diphosphonates; Female; Humans; Male; Middle Aged; Osteoblasts; RNA, Messenger; Time Factors; Physiology; Hematology||Issue Date:||2004||Project:||None||Journal:||BONE||Abstract:||
Bisphosphonates (BP's) are widely used in the treatment of a variety of bone-related diseases, particularly where the bone turnover is skewed in favor of osteolysis. The mechanisms by which BP's reduce bone resorption directly acting oil osteoclasts are now largely clarified even at molecular level. Researches concerning the BP's effects on osteoblast have instead shown variable results. Many in vitro studies have reported positive effects on osteoblasts proliferation and mineralization for several BPs, however, the observed effects differ, depending on the variety of different model system that has been used. Objectives. We have investigated if neridronate, an aminobisphosphonate suitable for pulsatory parenteral administration, could have an effect on human osteoblastic proliferation and differentiation in vitro. Methods. We have investigated whether prolonged addition of neridronate (from 10(-3) to 10(-11) M) to different human osteoblasts cultures, obtained from 14 different bone specimens, could affect the cells number, the endogenous cellular alkaline phosphatase (ALKP) activity, and the formation of mineralized nodules. Results. Our results show that neridronate does not negatively affect in vitro the viability, proliferation, and cellular activity of normal human osteoblasts even after a long period addition of the drug (20 days) at concentrations equal or lower than 10(-5) mol/l (therapeutic dose). In addition, neridronate seems to enhance the differentiation of cultured osteoblasts in mature bone-forming cells. A maximum increase of alkaline phosphatase activity (+50% after 10 days; P < 0.01) and mineralized nodules (+48% after 20 days; P < 0.05) was observed in cultures treated with neridronate 10(-8) M. Conclusions. These results encourage the use of neridronate in long-term therapy of demineralizing metabolic bone disorders.
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