Effects of a preferential myosin loss on Ca2+ activation of force generation in single human skeletal muscle fibres

被引:31
作者
Ochala, Julien [1 ]
Larsson, Lars [1 ,2 ]
机构
[1] Univ Uppsala Hosp, Dept Clin Neurophysiol, S-75185 Uppsala, Sweden
[2] Penn State Univ, Ctr Dev & Hlth Genet, University Pk, PA 16802 USA
关键词
D O I
10.1113/expphysiol.2007.041798
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Preferential loss of the motor protein myosin, as observed in patients with acute quadriplegic myopathy (AQM) or cancer cachexia, causes generalized muscle wasting, muscle weakness and a decrease in muscle fibre force normalized to cross-sectional area. It remains unclear, however, whether this myosin loss influences other important features of muscle fibre function, such as Ca2+ activation of the contractile proteins. To address this question, we have studied Ca2+ sensitivity of force generation using skinned muscle fibres from four patients with AQM or cancer cachexia and a preferential loss of myosin; and from seven healthy control individuals. Force and apparent rate constant of force redevelopment (k(tr)) were assessed in solutions with varying Ca2+ concentrations (pCa), allowing construction of relative force-pCa and k(tr)-pCa relationships. Results showed a rightward shift of the relative force-pCa relationship and a leftward shift of the relative k(tr)-pCa curve in muscle fibres with a preferential myosin loss. To improve the understanding of the mechanisms underlying these alterations, the relative stiffness-pCa relationship was evaluated. A rightward shift of this curve was observed, suggesting that the changes in the Ca2+ activation of force and k(tr) were predominantly due to a decrease in the relative number of attached cross-bridges at different pCa values. Thus, a change in Ca2+ activation of the contractile apparatus in patients with preferential myosin loss is proposed as an additional factor contributing to the muscle function impairment in these patients.
引用
收藏
页码:486 / 495
页数:10
相关论文
共 33 条
[1]   Cancer cachexia is regulated by selective targeting of skeletal muscle gene products [J].
Acharyya, S ;
Ladner, KJ ;
Nelsen, LL ;
Damrauer, J ;
Reiser, PJ ;
Swoap, S ;
Guttridge, DC .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (03) :370-378
[2]  
BANDUSEELA VC, 2007, EMC STOKH ABSTR, V5, P21
[3]   RATE OF FORCE GENERATION IN MUSCLE - CORRELATION WITH ACTOMYOSIN ATPASE ACTIVITY IN SOLUTION [J].
BRENNER, B ;
EISENBERG, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (10) :3542-3546
[4]   Rate constant of muscle force redevelopment reflects cooperative activation as well as cross-bridge kinetics [J].
Campbell, K .
BIOPHYSICAL JOURNAL, 1997, 72 (01) :254-262
[5]   MYOPATHY WITH THICK FILAMENT (MYOSIN) LOSS FOLLOWING PROLONGED PARALYSIS WITH VECURONIUM DURING STEROID TREATMENT [J].
DANON, MJ ;
CARPENTER, S .
MUSCLE & NERVE, 1991, 14 (11) :1131-1139
[6]   VELOCITY OF UNLOADED SHORTENING AND ITS RELATION TO SARCOMERE LENGTH AND ISOMETRIC FORCE IN VERTEBRATE MUSCLE-FIBERS [J].
EDMAN, KAP .
JOURNAL OF PHYSIOLOGY-LONDON, 1979, 291 (JUN) :143-159
[7]  
FABIATO A, 1988, METHOD ENZYMOL, V157, P378
[8]   Cooperative mechanisms in the activation dependence of the rate of force development in rabbit skinned skeletal muscle fibers [J].
Fitzsimons, DP ;
Patel, JR ;
Campbell, KS ;
Moss, RL .
JOURNAL OF GENERAL PHYSIOLOGY, 2001, 117 (02) :133-148
[9]  
Frontera WR, 1997, MUSCLE NERVE, V20, P948, DOI 10.1002/(SICI)1097-4598(199708)20:8<948::AID-MUS3>3.0.CO
[10]  
2-6