阿仑膦酸钠联合1 α -羟基维生素D3治疗老年大鼠卵巢切除术后骨质流失的疗效观察。

Masaya Ito, Y. Azuma, H. Takagi, K. Komoriya, T. Ohta, H. Kawaguchi
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引用次数: 40

摘要

我们研究了阿仑膦酸钠和1 α -羟基维生素D3 (1 α (OH)D3)联合用药对老年去卵巢大鼠骨量和骨强度的影响,并与单独用药比较。40周龄的雌性大鼠切除卵巢或假手术,15周后,切除卵巢的大鼠每天单独给药、阿仑膦酸钠(0.2或1.0 mg/kg,p.o.)、α (OH)D3(0.02微克/kg,p.o.)或阿仑膦酸钠和α (OH)D3联合0.2或1.0 mg/kg。12周后,联合治疗组与载具治疗组相比,第4腰椎和股骨中段的骨密度和机械强度显著增加,其效果几乎等于或略低于单独治疗组的效果。机械强度的增加与骨密度的增加成正比,这表明这些治疗对骨强度的刺激作用主要归因于对骨量的刺激作用。组织学、计算机断层扫描和生化标志物的分析证实了联合治疗对小梁骨的强烈影响,特别是与小梁数量增加和骨转换减少有关。我们建议每日联合阿仑膦酸钠和1 α (OH)D3作为一种治疗绝经后骨质疏松症的临床治疗是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Curative effect of combined treatment with alendronate and 1 alpha-hydroxyvitamin D3 on bone loss by ovariectomy in aged rats.
We investigated the combined effects of alendronate and 1alpha-hydroxyvitamin D3 (1alpha(OH)D3) on the bone mass and strength in aged ovariectomized rats and compared them with those of single treatments. Forty-week-old female rats underwent ovariectomy or sham operation, and after 15 weeks, ovariectomized rats were daily administered vehicle alone, alendronate (0.2 or 1.0 mg/kg,p.o.), 1alpha(OH)D3 (0.02 microg/kg, p.o.), or the combinations of 0.2 or 1.0 mg/kg of alendronate and 1alpha(OH)D3. After 12 weeks, the groups receiving combined treatments had significantly increased bone density and mechanical strength of the 4th lumbar vertebral body and the midfemur compared to the vehicle-treated group, and the effects were almost equal to or slightly less than the addition of those of the respective single treatments. The increase in mechanical strength was proportional to that in bone mineral density, suggesting that the stimulatory effects of these treatments on bone strength are ascribable primarily to those on bone mass. Analyses of histology, computed tomography, and biochemical markers confirmed the strong effect of the combined treatment on trabecular bone in particular, which was associated with increased trabecular number and decreased bone turnover. We propose that the combination of daily alendronate and 1alpha(OH)D3 is clinically promising as a curative treatment of established postmenopausal osteoporosis.
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