Use of iQPR-H.sub.2 O for bone regeneration and its potential in the improvement of osteoporosis

Background Current treatments for osteoporosis are associated with various side effects and do not prevent the age-related decrease in osteoblast number. The objective of this study was to evaluate the effects of iQPR-H.sub.2 O on osteogenesis. Methods Mouse fibroblast NIH3T3 and pre-osteoblastic MC...

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Veröffentlicht in:BMC musculoskeletal disorders 2011-10, Vol.12, p.227
Hauptverfasser: Lee, Chiming, Cheong, Meileng, Hsiao, Wentien, Liu, Henyu, Tsai, Chingyu, Wang, Mingfu, Wu, Chihhsiung, Chang, Kwanghwa, Lam, Gowlin, Deng, Winping
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Sprache:eng
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Zusammenfassung:Background Current treatments for osteoporosis are associated with various side effects and do not prevent the age-related decrease in osteoblast number. The objective of this study was to evaluate the effects of iQPR-H.sub.2 O on osteogenesis. Methods Mouse fibroblast NIH3T3 and pre-osteoblastic MC3T3-E1 cells were cultured in medium prepared with iQPR-H.sub.2 O or unprocessed mineral water (control cells), and proliferation and differentiation were assessed by MTT and alkaline phosphatase assay, respectively. Mineral deposition by the cells was determined using Alizarin red S staining. A mouse model of osteoporosis, ovariectomized SAMP8 mice, was used to evaluate the effects of iQPR-H.sub.2 O on osteogenesis in vivo. Mice were given either iQPR-H.sub.2 O or unprocessed mineral water (control group) for four months after which bone mass density (BMD) measurements were made using a bone densitometer and hematoxylin and eosin staining of bone samples. Results NIH3T3 cells grown in medium prepared with iQPR-H.sub.2 O exhibited significantly greater proliferation. NIH3T3 and MC3T3-E1 cells demonstrated a significant increase in alkaline phosphatase levels in the iQPR-H.sub.2 O group. MC3T3-E1 cells showed mineralization at day 28. mRNA expression levels of both osteopontin and runt-related transcription factor 2 in MC3T3-E1 cells were higher in the iQPR-H.sub.2 O group compared with the control group. After four months, significantly greater bone regeneration was evident in ovariectomized SAMP8 mice administered iQPR-H.sub.2 O as compared with control group. Conclusions iQPR-H.sub.2 O may reduce the symptoms of osteoporosis by improving osteogenesis.
ISSN:1471-2474
1471-2474
DOI:10.1186/1471-2474-12-227