Jeong Youngjae, Carleton Stephanie M, Gentry Bettina A, Yao Xiaomei, Ferreira J Andries, Salamango Daniel J, Weis MaryAnn, Oestreich Arin K, Williams Ashlee M, McCray Marcus G, Eyre David R, Brown Marybeth, Wang Yong, Phillips Charlotte L
Department of Biochemistry, University of Missouri, Columbia, MO, USA.
Department of Veterinary Pathobiology, University of Missouri, Columbia, MO, USA.
J Bone Miner Res. 2015 Oct;30(10):1874-86. doi: 10.1002/jbmr.2518. Epub 2015 May 14.
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder associated with reduced bone mineral density and skeletal fragility. Bone is inherently mechanosensitive, with bone strength being proportional to muscle mass and strength. Physically active healthy children accrue more bone than inactive children. Children with type I OI exhibit decreased exercise capacity and muscle strength compared with healthy peers. It is unknown whether this muscle weakness reflects decreased physical activity or a muscle pathology. In this study, we used heterozygous G610C OI model mice (+/G610C), which model both the genotype and phenotype of a large Amish OI kindred, to evaluate hindlimb muscle function and physical activity levels before evaluating the ability of +/G610C mice to undergo a treadmill exercise regimen. We found +/G610C mice hindlimb muscles do not exhibit compromised muscle function, and their activity levels were not reduced relative to wild-type mice. The +/G610C mice were also able to complete an 8-week treadmill regimen. Biomechanical integrity of control and exercised wild-type and +/G610C femora were analyzed by torsional loading to failure. The greatest skeletal gains in response to exercise were observed in stiffness and the shear modulus of elasticity with alterations in collagen content. Analysis of tibial cortical bone by Raman spectroscopy demonstrated similar crystallinity and mineral/matrix ratios regardless of sex, exercise, and genotype. Together, these findings demonstrate +/G610C OI mice have equivalent muscle function, activity levels, and ability to complete a weight-bearing exercise regimen as wild-type mice. The +/G610C mice exhibited increased femoral stiffness and decreased hydroxyproline with exercise, whereas other biomechanical parameters remain unaffected, suggesting a more rigorous exercise regimen or another exercise modality may be required to improve bone quality of OI mice.
成骨不全症(OI)是一种异质性遗传性结缔组织疾病,与骨矿物质密度降低和骨骼脆弱性相关。骨骼具有内在的机械敏感性,骨强度与肌肉质量和力量成正比。身体活跃的健康儿童比不活跃的儿童积累更多的骨量。与健康同龄人相比,I型OI患儿的运动能力和肌肉力量下降。目前尚不清楚这种肌肉无力是反映身体活动减少还是肌肉病变。在本研究中,我们使用杂合G610C OI模型小鼠(+/G610C),该模型模拟了一个大型阿米什OI家族的基因型和表型,在评估+/G610C小鼠进行跑步机运动方案的能力之前,先评估其下肢肌肉功能和身体活动水平。我们发现+/G610C小鼠的后肢肌肉没有表现出受损的肌肉功能,并且它们的活动水平相对于野生型小鼠没有降低。+/G610C小鼠也能够完成为期8周的跑步机运动方案。通过扭转加载至破坏来分析对照、运动后的野生型和+/G610C股骨的生物力学完整性。在刚度和弹性剪切模量方面观察到对运动的最大骨骼增益,同时胶原含量发生改变。通过拉曼光谱对胫骨皮质骨进行分析表明,无论性别、运动和基因型如何,结晶度和矿物质/基质比率相似。总之,这些发现表明+/G610C OI小鼠与野生型小鼠具有同等的肌肉功能、活动水平和完成负重运动方案的能力。+/G610C小鼠在运动后股骨刚度增加,羟脯氨酸减少,而其他生物力学参数未受影响,这表明可能需要更严格的运动方案或另一种运动方式来改善OI小鼠的骨质量。