Contractile properties of single permeabilized muscle fibers from congenital cleft palates and normal palates of Spanish goats

Plastic and Reconstructive Surgery

Volumn 119, Issue 6, 2007, Pages 1685-1694

  Hanes, Michael C ^b   Weinzweig, Jeffrey ^b   Kuzon, William M ^b   Panter, Kip E ^b   Buchman, Steven R ^b   Faulkner, John A ^b   Yu, Deborah ^b   Cederna, Paul S ^b   Larkin, Lisa M ^a  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; CALCULATION; CLEFT PALATE; COMPARATIVE STUDY; CONTROLLED STUDY; FEMALE; FORCE; GOAT; MUSCLE CONTRACTILITY; MUSCLE FATIGUE; MUSCLE FIBER CONTRACTION; MUSCLE ISOMETRIC CONTRACTION; NONHUMAN; PALATOPHARYNGEAL INCOMPETENCE; PRIORITY JOURNAL;

ANALYSIS OF VARIANCE; ANIMALS; ANIMALS, NEWBORN; CLEFT PALATE; DISEASE MODELS, ANIMAL; FEMALE; GOATS; IMMUNOHISTOCHEMISTRY; ISOMETRIC CONTRACTION; MUSCLE FATIGUE; MUSCLE FIBERS; ORGAN CULTURE TECHNIQUES; PALATAL MUSCLES; PROBABILITY; RANDOM ALLOCATION; REFERENCE VALUES; SENSITIVITY AND SPECIFICITY; SPAIN; STATISTICS, NONPARAMETRIC;

EID: 34247351689     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.prs.0000258832.84261.37     Document Type: Article

References (23)

1. Forrester, M. B., and Merz, R. D. Descriptive epidemiology of oral clefts in a multiethnic population, Hawaii, 1986-2000. Cleft Palate Craniofac. J. 41: 622, 2004.
2. Elahi, M. M., Jackson, I. T., Elahi, O., et al. Epidemiology of cleft lip and cleft palate in Pakistan. Plast. Reconstr. Surg. 113: 1548, 2004.
3. Becker, D. B., Grames, L. M., Pilgram, T., et al. The effect of timing of surgery for velopharyngeal dysfunction on speech. J. Craniofac. Surg. 15: 804, 2004.
4. McWilliams, B. J., Randall, P., LaRossa, D., et al. Speech characteristics associated with the Furlow palatoplasty as compared with other surgical techniques. Plast. Reconstr. Surg. 98: 610, 1996.
5. Shaw, W. C., Dahl, E., Asher-McDade, C., et al. A six-center international study of treatment outcome in patients with clefts of the lip and palate: Part 5. General discussion and conclusions. Cleft Palate Craniofac. J. 29: 413, 1992.
6. Cohen, S. R., Chen, L. L., Burdi, A. R., et al. Patterns of abnormal myogenesis in human cleft palates. Cleft Palate Craniofac. J. 31: 345, 1994.
7. Schendel, S. A., Cholon, A., and Delaire, J. Histochemical analysis of cleft palate muscle. Plast. Reconstr. Surg. 94: 919, 1994.
8. Weinzweig, J., Panter, K. E., Spangenberger, A., et al. The fetal cleft palate: III. Ultrastructural and functional analysis of palatal development following in utero repair of the congenital model. Plast. Reconstr. Surg. 109: 2355, 2002.
9. Macpherson, P. C., Schork, M. A., and Faulkner, J. A. Contraction-induced injury to single fiber segments from fast and slow muscles of rats by single stretches. Am. J. Physiol. 271: C1438, 1996.
10. Macpherson, P. C., Dennis, R. G., and Faulkner, J. A. Sarcomere dynamics and contraction-induced injury to maximally activated single muscle fibres from soleus muscles of rats. J. Physiol. 500: 523, 1997.
11. Tachimura, T., Nohara, K., Satoh, K., et al. Evaluation of fatigability of the levator veli palatini muscle during continuous blowing using power spectra analysis. Cleft Palate Craniofac. J. 41: 320, 2004.
12. Weinzweig, J., Panter, K. E., Pantaloni, M., et al. The fetal cleft palate: I. Characterization of a congenital model. Plast. Reconstr. Surg. 103: 419, 1999.
13. Moisescu, D. G., and Thieleczek, R. Calcium and strontium concentration changes within skinned muscle preparations following a change in the external bathing solution. J. Physiol. 275: 241, 1978.
14. Wahr, P. A., and Rall, J. A. Role of calcium and cross bridges in determining rate of force development in frog muscle fibers. Am. J. Physiol. 272: C1664, 1997.
15. Burton, K., White, H., and Sleep, J. Kinetics of muscle contraction and actomyosin NTP hydrolysis from rabbit using a series of metal-nucleotide substrates. J. Physiol. 563: 689, 2005.
16. Swartz, D. R., and Moss, R. L. Influence of a strong-binding myosin analogue on calcium-sensitive mechanical properties of skinned skeletal muscle fibers. J. Biol. Chem. 267: 20497, 1992.
17. Brenner, B. Technique for stabilizing the striation pattern in maximally calcium-activated skinned rabbit psoas fibers. Biophys. J. 41: 99, 1983.
18. Lindman, R., Paulin, G., and Stal, P. S. Morphological characterization of the levator veli palatini muscle in children born with cleft palates. Cleft Palate Craniofac. J. 38: 438, 2001.
19. Wigmore, P. M., and Evans, D. J. Molecular and cellular mechanisms involved in the generation of fiber diversity during myogenesis. Int. Rev. Cytol. 216: 175, 2002.
20. Ohira, Y., Yoshinaga, T., Nomura, T., et al. Gravitational unloading effects on muscle fiber size, phenotype and myonuclear number. Adv. Space Res. 30: 777, 2002.
21. Widrick, J. J., Trappe, S. W., Blaser, C. A., et al. Isometric force and maximal shortening velocity of single muscle fibers from elite master runners. Am. J. Physiol. 271: C666, 1996.
22. Widrick, J. J., Trappe, S. W., Costill, D. L., et al. Force-velocity and force-power properties of single muscle fibers from elite master runners and sedentary men. Am. J. Physiol. 271: C676, 1996.
23. Gonzalez, E., and Delbono, O. Age-dependent fatigue in single intact fast and slow fibers from mouse EDL and soleus skeletal muscles. Mech. Ageing Dev. 122: 1019, 2001.