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预先使用维生素 K(2)可显著提高利塞膦酸钠的疗效。

Prior treatment with vitamin K(2) significantly improves the efficacy of risedronate.

机构信息

Division of Radiology, Department of Maxillofacial Diagnostic Science, Kanagawa Dental College, 82 Inaokacho, Yokosuka, Kanagawa, 238-8580, Japan.

出版信息

Osteoporos Int. 2009 Nov;20(11):1863-72. doi: 10.1007/s00198-009-0888-z. Epub 2009 Mar 12.

Abstract

UNLABELLED

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 microg 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ovariectomized at 9-week, were treated for 8 weeks with R, K, or R plus K (R/K), and then, either the treatment was withdrawn (WO) or switched to K or R in the case of R and K. After another 8 weeks, the mice were killed, and mechanical tests and analyses of femur properties by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.

摘要

未标记

MK-4 预处理 8 周,继以利塞膦酸钠治疗 8 周,可预防单一药物的不足,显著增加去卵巢 ICR 小鼠股骨的强度,与去卵巢(OVX)对照组相比。MK-4 继利塞膦酸钠或同时给药可能不推荐,因为它们带来的益处最小。

介绍

本研究的目的是确定利塞膦酸钠 0.25mg/kg/天(R)与维生素 K2 约 100μg MK-4/kg/天(K)联合应用的最佳组合,以改善骨质疏松症小鼠骨的强度。

方法

13 周龄 ICR 小鼠,9 周时去卵巢,用 R、K 或 R+K(R/K)治疗 8 周,然后停药(WO)或 R 和 K 切换治疗。8 周后,处死小鼠,进行力学试验和股骨特性分析,采用外周定量 CT、微焦点 X 射线管 CT 和共聚焦激光拉曼微光谱仪。

结果

K 到 R 股骨在材料性能、骨矿物质密度、BMC、小梁结构和皮质几何形状等参数上均优于对照组。K 停药后发生的横截面对矩惯性增加,被利塞膦酸钠预防。除 K 到 R 外,R 到 WO 骨干和 K 到 WO 骨骺的一些特性明显优于 OVX 对照组。

结论

MK-4 预处理继以利塞膦酸钠治疗可显著增加股骨强度,与 OVX 对照组相比。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e752/2765650/c576767c3c9b/198_2009_888_Fig1_HTML.jpg

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