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Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate
SUMMARY: Prior 8-week treatment with menatetrenone, MK-4, followed by 8-week risedronate prevented the shortcomings of individual drugs and significantly increased the strength of ovariectomized ICR mouse femur compared to the ovariectomized (OVX) controls. Neither MK-4 following risedronate nor the...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765650/ https://www.ncbi.nlm.nih.gov/pubmed/19280272 http://dx.doi.org/10.1007/s00198-009-0888-z |
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author | Matsumoto, Y. Mikuni-Takagaki, Y. Kozai, Y. Miyagawa, K. Naruse, K. Wakao, H. Kawamata, R. Kashima, I. Sakurai, T. |
author_facet | Matsumoto, Y. Mikuni-Takagaki, Y. Kozai, Y. Miyagawa, K. Naruse, K. Wakao, H. Kawamata, R. Kashima, I. Sakurai, T. |
author_sort | Matsumoto, Y. |
collection | PubMed |
description | SUMMARY: Prior 8-week treatment with menatetrenone, MK-4, followed by 8-week risedronate prevented the shortcomings of individual drugs and significantly increased the strength of ovariectomized ICR mouse femur compared to the ovariectomized (OVX) controls. Neither MK-4 following risedronate nor the concomitant administration may be recommended because they brought the least beneficial effect. INTRODUCTION: The objective of this study was to determine the best combinatory administration of risedronate at 0.25 mg/kg/day (R) with vitamin K(2) at approximately 100 μg MK-4/kg/day (K) to improve strength of osteoporotic mouse bone. METHODS: Thirteen-week-old ICR mice, ovariectomized at 9-week, were treated for 8 weeks with R, K, or R plus K (R/K), and then, either the treatment was withdrawn (WO) or switched to K or R in the case of R and K. After another 8 weeks, the mice were killed, and mechanical tests and analyses of femur properties by peripheral quantitative computed tomography, microfocus X-ray tube computed tomography, and confocal laser Raman microspectroscopy were carried out. RESULTS: The K to R femur turned out superior in parameters tested such as material properties, bone mineral density, BMC, trabecular structure, and geometry of the cortex. The increased cross-sectional moment of inertia, which occurred after K withdrawal, was prevented by risedronate in K to R. In addition to K to R, some properties of R to WO diaphysis and K to WO epiphysis were significantly better than OVX controls. CONCLUSION: Prior treatment with MK-4 followed by risedronate significantly increased femur strength in comparison to the OVX controls. |
format | Text |
id | pubmed-2765650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-27656502009-10-23 Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate Matsumoto, Y. Mikuni-Takagaki, Y. Kozai, Y. Miyagawa, K. Naruse, K. Wakao, H. Kawamata, R. Kashima, I. Sakurai, T. Osteoporos Int Original Article SUMMARY: Prior 8-week treatment with menatetrenone, MK-4, followed by 8-week risedronate prevented the shortcomings of individual drugs and significantly increased the strength of ovariectomized ICR mouse femur compared to the ovariectomized (OVX) controls. Neither MK-4 following risedronate nor the concomitant administration may be recommended because they brought the least beneficial effect. INTRODUCTION: The objective of this study was to determine the best combinatory administration of risedronate at 0.25 mg/kg/day (R) with vitamin K(2) at approximately 100 μg MK-4/kg/day (K) to improve strength of osteoporotic mouse bone. METHODS: Thirteen-week-old ICR mice, ovariectomized at 9-week, were treated for 8 weeks with R, K, or R plus K (R/K), and then, either the treatment was withdrawn (WO) or switched to K or R in the case of R and K. After another 8 weeks, the mice were killed, and mechanical tests and analyses of femur properties by peripheral quantitative computed tomography, microfocus X-ray tube computed tomography, and confocal laser Raman microspectroscopy were carried out. RESULTS: The K to R femur turned out superior in parameters tested such as material properties, bone mineral density, BMC, trabecular structure, and geometry of the cortex. The increased cross-sectional moment of inertia, which occurred after K withdrawal, was prevented by risedronate in K to R. In addition to K to R, some properties of R to WO diaphysis and K to WO epiphysis were significantly better than OVX controls. CONCLUSION: Prior treatment with MK-4 followed by risedronate significantly increased femur strength in comparison to the OVX controls. Springer-Verlag 2009-03-12 2009 /pmc/articles/PMC2765650/ /pubmed/19280272 http://dx.doi.org/10.1007/s00198-009-0888-z Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Matsumoto, Y. Mikuni-Takagaki, Y. Kozai, Y. Miyagawa, K. Naruse, K. Wakao, H. Kawamata, R. Kashima, I. Sakurai, T. Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate |
title | Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate |
title_full | Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate |
title_fullStr | Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate |
title_full_unstemmed | Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate |
title_short | Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate |
title_sort | prior treatment with vitamin k(2) significantly improves the efficacy of risedronate |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765650/ https://www.ncbi.nlm.nih.gov/pubmed/19280272 http://dx.doi.org/10.1007/s00198-009-0888-z |
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