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Effects of minodronic acid and alendronate on bone remodeling, Microdamage accumulation, Degree of mineralization and bone mechanical properties in ovariectomized cynomolgus monkeys

机译:米诺膦酸和阿仑膦酸盐对去卵巢食蟹猕猴骨重塑,微损伤累积,矿化程度和骨力学性能的影响

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Suppression of bone remodeling by bisphosphonates leads to accumulation of microdamage in bone. If this microdamage develops due to suppressed repair of remodeling only, more potent bisphosphonates should cause more damage. In this study, we evaluated the effects of reduced bone turnover produced by a potent bisphosphonate, minodronic acid, on microdamage accumulation, the degree of mineralization and mechanical properties of bone in ovariectomized cynomolgus monkeys, and compared these effects with those of alendronate. Sixty female monkeys aged 9-17. years old were divided into five groups. The sham group and the ovariectomized group were treated daily for 17. months with lactose vehicle. The other three groups were treated daily with minodronic acid at a dose of 0.015. mg/kg or 0.15. mg/kg, or alendronate at 0.5. mg/kg orally. After sacrifice, lumbar vertebrae and left femurs were subjected to histomorphometry, microdamage, mineralization analyses, and mechanical testing. Minodronic acid suppressed bone remodeling of cancellous and cortical bone in a dose-dependent manner and the higher dose of minodronic acid suppressed bone remodeling more strongly than alendronate. The lower dose of minodronic acid did not increase microdamage accumulation and compressive strength, but the higher dose of minodronic acid and alendronate resulted in similar increases in cancellous microdamage accumulation and ultimate load in lumbar vertebra. There were no significant differences among the groups in microdamage, degree of mineralization and mechanical properties in cortical bone of the femoral shaft; however, only alendronate showed a tendency to increase highly mineralized osteons and microdamage. These findings suggest that microdamage caused by minodronic acid is less than that expected based on the extent of remodeling suppression, in comparison with alendronate although this was not reflected in any significant change of mechanical properties. ? 2013 Elsevier Inc.
机译:双膦酸盐抑制骨重塑导致骨中微损伤的积累。如果这种微损伤仅由于抑制了重塑的修复而发展,则更有效的双膦酸酯应造成更大的损害。在这项研究中,我们评估了有效的双膦酸盐,米诺膦酸对减少卵巢切除的食蟹猕猴的微损伤累积,骨矿化程度和骨骼的机械特性产生的骨转换的影响,并将这些影响与阿仑膦酸盐进行了比较。 9至17岁的60只母猴。岁以下分为五个组。假手术组和去卵巢组每天用乳糖载体治疗17个月。其他三组每天接受米诺膦酸0.015剂量的治疗。 mg / kg或0.15。毫克/公斤或阿仑膦酸盐0.5。口服mg / kg。处死后,对腰椎和左股骨进行组织形态测定,微损伤,矿化分析和机械测试。米诺膦酸以剂量依赖的方式抑制松质骨和皮质骨的骨重塑,而更高剂量的米诺膦酸比阿仑膦酸盐更能抑制骨重塑。较低剂量的米诺膦酸不会增加微损伤的积累和抗压强度,但是较高剂量的米诺膦酸和阿仑膦酸盐会导致类似的松质微损伤积累和腰椎最终负荷的增加。各组之间在股骨干皮质骨的微损伤,矿化程度和力学性能方面无显着差异。然而,只有阿仑膦酸盐显示出增加高度矿化的骨质和微损伤的趋势。这些发现表明,与阿仑膦酸盐相比,米诺膦酸引起的微损伤小于基于重塑抑制程度的预期,尽管这并未反映在机械性能的任何显着变化中。 ? 2013爱思唯尔公司

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