Novotny S A, Warren G L, Lin A S, Guldberg R E, Baltgalvis K A, Lowe D A
Department of Kinesiology, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J Musculoskelet Neuronal Interact. 2012 Mar;12(1):16-23.
The purpose of this study was to determine the extent to which prednisolone treatment and restricted physical activity caused deleterious changes in inherently compromised mdx bone.
Four week-old male mdx mice (n=36) were treated for 8-wk either with or without prednisolone (0.8-1.3 mg/kg/d) and were housed in traditional or small cages (restricted activity). Tibial bone strength, geometry, and intrinsic material properties were assessed at the mid-shaft by three-point bending and micro-computed tomography (μCT).
Three-point bending results showed that both prednisolone and restricted activity reduced bone strength (7%), however stiffness was only reduced in restricted-activity mice. μCT analyses showed that cortical bone area and cortical thickness were 13% smaller in restricted-activity mice, and may have accounted for their compromised bone strength. Intrinsic material properties, including volumetric bone mineral density (vBMD) and modulus of elasticity, were not impacted by either treatment, however, vBMD tended to be lower in restricted-activity mice (p=0.06).
These data show that prednisolone treatment and restricted physical activity independently accentuate reductions in the strength and geometry of mdx bone, but do not influence intrinsic material properties.
本研究旨在确定泼尼松龙治疗和限制体力活动在多大程度上会对先天受损的mdx小鼠骨骼造成有害变化。
将4周龄雄性mdx小鼠(n = 36)分为两组,一组接受为期8周的泼尼松龙治疗(0.8 - 1.3毫克/千克/天),另一组不接受治疗,两组小鼠分别饲养在传统大小或小笼子中(限制活动)。通过三点弯曲试验和微型计算机断层扫描(μCT)评估小鼠胫骨中段的骨强度、几何形状和内在材料特性。
三点弯曲试验结果显示,泼尼松龙治疗和限制活动均使骨强度降低了7%,然而,只有限制活动组小鼠的骨硬度降低。μCT分析表明,限制活动组小鼠的皮质骨面积和皮质厚度减小了13%,这可能是其骨强度受损的原因。包括骨体积密度(vBMD)和弹性模量在内的内在材料特性均未受到任何一种治疗的影响,不过,限制活动组小鼠的vBMD有降低趋势(p = 0.06)。
这些数据表明,泼尼松龙治疗和限制体力活动各自都会加剧mdx小鼠骨骼强度和几何形状的降低,但不影响其内在材料特性。