Contractile properties and susceptibility to exercise-induced damage of normal and mdx mouse tibialis anterior muscle.

作者: P. Sacco , D. A. Jones , J. R. T. Dick , G. Vrbová

DOI: 10.1042/CS0820227

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摘要: 1. The functional properties of tibialis anterior muscles normal adult (C57BL/10) and age-matched dystrophin-deficient (C57BL/10 mdx) mice have been investigated in situ. Comparisons were made between muscle strength, rates force development relaxation, force-frequency responses fatiguability. Subjecting mdx C57 to a regimen eccentric exercise allowed the hypothesis be tested that are more susceptible exercise-induced damage. 2. were, on average, 30% stronger than almost 80% heavier, but both had similar lengths. Thus, although absolute terms, their estimated per unit cross-sectional area was significantly less muscles. 3. relationships differed whilst, at 40 Hz, former developed 70% 100 latter only 55% maximal force. Twitch muscles, contraction time shortened, consequent reduction fusion frequency probably explains differences observed two groups. 4. fatiguable when stimulated repeatedly Hz. It is possible lower relative Hz entailed energy demand thus slower rate fatigue seen 5. Eccentrically exercised showed large loss for up 12 days after exercise. Maximal occurred 3 (55% non-exercised muscle), which also corresponded with period greatest fibre necrosis. reduced Hz/100 ratio 1 This primarily due twitch amplitude rather change course twitch. unlikely, therefore, altered contractile characteristics result presence damaged otherwise fibres. 6. displayed degrees Furthermore, recovery nadir very By exercise, recovered 76% control respectively. Our findings do not support

参考文章(12)
D. A. Jones, Muscle Fatigue Due to Changes Beyond the Neuromuscular Junction Novartis Foundation Symposia. ,vol. 82, pp. 178- 196 ,(1981) , 10.1002/9780470715420.CH11
C. G. Carlson, R. V. Makiejus, A noninvasive procedure to detect muscle weakness in the mdx mouse Muscle & Nerve. ,vol. 13, pp. 480- 484 ,(1990) , 10.1002/MUS.880130603
John A. Faulkner, David A. Jones, Joan M. Round, INJURY TO SKELETAL MUSCLES OF MICE BY FORCED LENGTHENING DURING CONTRACTIONS Quarterly Journal of Experimental Physiology. ,vol. 74, pp. 661- 670 ,(1989) , 10.1113/EXPPHYSIOL.1989.SP003318
J. E. Anderson, W. K. Ovalle, B. H. Bressler, Electron microscopic and autoradiographic characterization of hindlimb muscle regeneration in the mdx mouse. Anatomical Record-advances in Integrative Anatomy and Evolutionary Biology. ,vol. 219, pp. 243- 257 ,(1987) , 10.1002/AR.1092190305
Josette Dangain, Gerta Vrbova, Muscle development in mdx mutant mice Muscle & Nerve. ,vol. 7, pp. 700- 704 ,(1984) , 10.1002/MUS.880070903
G. R. COULTON, N. A. CURTIN, J. E. MORGAN, T. A. PARTRIDGE, The mdx mouse skeletal muscle myopathy: II. Contractile properties. Neuropathology and Applied Neurobiology. ,vol. 14, pp. 299- 314 ,(1988) , 10.1111/J.1365-2990.1988.TB00890.X
J. Fridén, M. Sjöström, B. Ekblom, A morphological study of delayed muscle soreness. Cellular and Molecular Life Sciences. ,vol. 37, pp. 506- 507 ,(1981) , 10.1007/BF01986165
Eric P. Hoffman, Robert H. Brown, Louis M. Kunkel, Dystrophin: The protein product of the duchenne muscular dystrophy locus Cell. ,vol. 51, pp. 919- 928 ,(1987) , 10.1016/0092-8674(87)90579-4
G. Bulfield, W. G. Siller, P. A. Wight, K. J. Moore, X chromosome-linked muscular dystrophy (mdx) in the mouse. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 81, pp. 1189- 1192 ,(1984) , 10.1073/PNAS.81.4.1189
J M Round, D A Jones, R H Edwards, A flexible microprocessor system for the measurement of cell size. Journal of Clinical Pathology. ,vol. 35, pp. 620- 624 ,(1982) , 10.1136/JCP.35.6.620