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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Suppressed bone turnover by long-term bisphosphonate treatment accumulates microdamage but maintains intrinsic material properties in cortical bone of dog rib.
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Suppressed bone turnover by long-term bisphosphonate treatment accumulates microdamage but maintains intrinsic material properties in cortical bone of dog rib.

机译:长期使用双膦酸盐治疗抑制骨转换,可累积微损伤,但可保持狗肋骨皮质骨的内在物质特性。

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摘要

Effects of long-term suppression of bone remodeling by bisphosphonate were investigated in cortical bone of dog rib. Although microdamage was accumulated, BMD was increased without increasing cortical bone area. Consequently, the intrinsic material properties were not reduced. INTRODUCTION: Recently, we have reported that long-term suppression of bone remodeling increases microdamage accumulation but is not necessarily associated with vertebral fragility because of compensated increase of bone mass and improved microarchitecture. This study aimed to investigate the effect of long-term suppression of bone remodeling by bisphosphonate on the degree of mineralization, accumulation of microdamage, and mechanical properties of cortical bone in the same dogs. MATERIALS AND METHODS: Twenty-nine 1-year-old beagles (15 males, 14 females) were divided into three groups and treated daily with vehicle (CNT) or with incadronate at a dose of 0.3 (LOW) or 0.6 mg/kg/day (HIGH) orally for 3 years. After death, pQCT, histomorphometry, microdamage measurements, and three-point bending mechanical test were performed using the ninth rib. RESULTS: Cortical BMD was increased in the incadronate-treated groups. Cortical activation frequency was suppressed by 82% and 70% in HIGH and LOW, respectively, compared with CNT, without impairment of mineralization. Microdamage accumulation was increased in both incadronate-treated groups. Although there were no significant differences in total and cortical area among the three groups, structural mechanical properties were significantly increased after incadronate treatment while intrinsic material properties were not changed in the incadronate-treated groups. CONCLUSION: This study suggests that long-term suppression of bone remodeling by bisphosphonate increases microdamage accumulation. However, this was not necessarily associated with a reduction of intrinsic material properties probably because of an increased degree of mineralization.
机译:研究了双膦酸盐对狗肋骨皮质骨长期抑制骨重塑的作用。尽管累积了微损伤,但BMD却增加了,而皮质骨面积却没有增加。因此,固有材料性能没有降低。引言:最近,我们报道长期抑制骨重塑会增加微损伤的积累,但由于骨量的增加和微结构的改善,不一定与椎骨脆性有关。这项研究旨在调查长期抑制双膦酸盐对同一只狗的矿化程度,微损伤的累积和皮质骨的力学性能的影响。材料与方法:将29只1岁的小猎犬(雄性15只,雌性14只)分为三组,每天用赋形剂(CNT)或加成剂量为0.3(LOW)或0.6 mg / kg /一天(HIGH)口服3年。死亡后,使用第九肋骨进行pQCT,组织形态测定,微损伤测量和三点弯曲力学测试。结果:钙盐治疗组中的皮质骨密度增加。与CNT相比,HIGH和LOW中的皮质激活频率分别被抑制了82%和70%,而没有矿化的损害。在两个用钙盐酸盐处理的组中,微损伤的积累都增加了。尽管三组的总面积和皮层面积没有显着差异,但在进行了钙盐处理后,结构力学性能显着提高,而在钙盐处理组中,固有材料性能没有变化。结论:这项研究表明,双膦酸盐对骨重塑的长期抑制会增加微损伤的积累。但是,这不一定与材料固有特性的降低有关,这可能是由于矿化程度提高了。

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