成年雌性 C57Bl/6 小鼠的小梁骨而非皮质骨对体内机械加载的反应减弱,与变形对负荷的减少相一致。
Diminished response to in vivo mechanical loading in trabecular and not cortical bone in adulthood of female C57Bl/6 mice coincides with a reduction in deformation to load.
机构信息
Julius Wolff Institut, Charité-Universitätsmedizin Berlin, Germany.
出版信息
Bone. 2013 Aug;55(2):335-46. doi: 10.1016/j.bone.2013.04.023. Epub 2013 May 1.
Bone loss occurs during adulthood in both women and men and affects trabecular bone more than cortical bone. The mechanism responsible for trabecular bone loss during adulthood remains unexplained, but may be due at least in part to a reduced mechanoresponsiveness. We hypothesized that trabecular and cortical bone would respond anabolically to loading and that the bone response to mechanical loading would be reduced and the onset delayed in adult compared to postpubescent mice. We evaluated the longitudinal adaptive response of trabecular and cortical bone in postpubescent, young (10 week old) and adult (26 week old) female C57Bl/6J mice to axial tibial compression using in vivo microCT (days 0, 5, 10, and 15) and dynamic histomorphometry (day 15). Loading elicited an anabolic response in both trabecular and cortical bone in young and adult mice. As hypothesized, trabecular bone in adult mice exhibited a reduced and delayed response to loading compared to the young mice, apparent in trabecular bone volume fraction and architecture after 10 days. No difference in mechanoresponsiveness of the cortical bone was observed between young and adult mice. Finite element analysis showed that load-induced strain was reduced with age. Our results suggest that trabecular bone loss that occurs in adulthood may in part be due to a reduced mechanoresponsiveness in this tissue and/or a reduction in the induced tissue deformation which occurs during habitual loading. Therapeutic approaches that address the mechanoresponsiveness of the bone tissue may be a promising and alternate strategy to maintain trabecular bone mass during aging.
在女性和男性成年期都会发生骨丢失,并且小梁骨比皮质骨更容易受到影响。导致成年期小梁骨丢失的机制尚不清楚,但可能至少部分是由于机械反应性降低所致。我们假设小梁骨和皮质骨对加载会产生合成代谢反应,并且与青春期后小鼠相比,成年小鼠对机械加载的骨反应会减少,并且发病时间会延迟。我们使用体内 microCT(第 0、5、10 和 15 天)和动态组织形态计量学(第 15 天)评估了青春期后、年轻(10 周龄)和成年(26 周龄)雌性 C57Bl/6J 小鼠胫骨轴向压缩的小梁骨和皮质骨的纵向适应性反应。加载在年轻和成年小鼠的小梁骨和皮质骨中均引起合成代谢反应。正如假设的那样,与年轻小鼠相比,成年小鼠的小梁骨对加载的反应减少且延迟,在 10 天后可见小梁骨体积分数和结构的变化。年轻和成年小鼠的皮质骨对机械反应性没有差异。有限元分析显示,随着年龄的增长,负荷引起的应变减少。我们的结果表明,成年期发生的小梁骨丢失可能部分是由于该组织的机械反应性降低以及在习惯性加载过程中发生的诱导组织变形减少所致。针对骨组织机械反应性的治疗方法可能是一种有前途的替代策略,可以在衰老过程中维持小梁骨量。