Bone is functionally impaired in dystrophic mice but less so than skeletal muscle

被引:38
|
作者
Novotny, Susan A. [1 ]
Warren, Gordon L. [2 ]
Lin, Angela S. [3 ]
Guldberg, Robert E. [3 ]
Baltgalvis, Kristen A. [4 ]
Lowe, Dawn A. [5 ]
机构
[1] Univ Minnesota, Dept Kinesiol, Minneapolis, MN 55455 USA
[2] Georgia State Univ, Div Phys Therapy, Atlanta, GA 30303 USA
[3] Georgia Inst Technol, Inst Bioengn & Biosci, Atlanta, GA 30332 USA
[4] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Program Phys Therapy & Rehabil Sci, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
Duchenne muscular dystrophy; Bone geometry; mu CT; Bone strength; Mdx mouse; MINERAL DENSITY; LIFE-SPAN; MDX; SOLEUS; BOYS; CONTRACTILITY; DEFICIENT; UTROPHIN; MASS;
D O I
10.1016/j.nmd.2010.12.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The primary purpose of this study was to determine if tibial bone strength is compromised in dystrophic mice and if so, what geometric and material properties contribute. Results of three-point bending tests showed that tibia of mdx and dko (dystrophin- and utrophin-deficient) mice had up to 50% lower strength and stiffness compared to wild-type mice. Micro-computed tomography indicated that dystrophic tibia had reductions of 6-57% in cortical cross-sectional moment of inertia and cross-sectional area. Metaphyseal trabecular bone morphometry was also altered up to 78% in dystrophic mice. Bone-to-muscle functional ratios (i.e., three-point bending measures:muscle strength) indicated that bone strength was relatively high in 7-week-old dystrophic mice compared to muscle strength, but ratios were similar to wild-type mice by 24 months of age. Young dystrophic mice have compromised bone strength; these models may be useful for designing therapeutic regimens aimed at improving the skeleton. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 193
页数:11
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