Twitch and tetanic force responses and longitudinal propagation of action potentials in skinned skeletal muscle fibres of the rat

1 Transverse electrical field stimulation (50 V cm−1, 2 ms duration) of mechanically skinned skeletal muscle fibres of the rat elicited twitch and tetanic force responses (36 ± 4 and 83 ± 4 % of maximum Ca2+‐activated force, respectively; n= 23) closely resembling those in intact fibres. The responses were steeply dependent on the field strength and were eliminated by inclusion of 10 μm tetrodotoxin (TTX) in the (sealed) transverse tubular (T‐) system of the skinned fibres and by chronic depolarisation of the T‐system. 2 Spontaneous twitch‐like activity occurred sporadically in many fibres, producing near maximal force in some instances (mean time to peak: 190 ± 40 ms; n= 4). Such responses propagated as a wave of contraction longitudinally along the fibre at a velocity of 13 ± 3 mm s−1 (n= 7). These spontaneous contractions were also inhibited by inclusion of TTX in the T‐system and by chronic depolarisation. 3 We examined whether the T‐tubular network was interconnected longitudinally using fibre segments that were skinned for only ∼2/3 of their length, leaving the remainder of each segment intact with its T‐system open to the bathing solution. After such fibres were exposed to TTX (60 μm), the adjacent skinned region (with its T‐system not open to the solution) became unresponsive to subsequent electrical stimulation in ∼50 % of cases (7/15), indicating that TTX was able to diffuse longitudinally inside the fibre via the tubular network over hundreds of sarcomeres. 4 These experiments show that excitation–contraction coupling in mammalian muscle fibres involves action potential propagation both transversally and longitudinally within the tubular system. Longitudinal propagation of action potentials inside skeletal muscle fibres is likely to be an important safety mechanism for reducing conduction failure during fatigue and explains why, in developing skeletal muscle, the T‐system first develops as an internal longitudinal network.

[1]  C. Franzini-armstrong,et al.  Structure and development of E-C coupling units in skeletal muscle. , 1994, Annual review of physiology.

[2]  J. Rall Role of Parvalbumin in Skeletal Muscle Relaxation , 1996 .

[3]  A. Herrmann-Frank,et al.  The role of Ca2+ ions in excitation-contraction coupling of skeletal muscle fibres. , 1995, Biochimica et biophysica acta.

[4]  F. Bezanilla,et al.  Sodium dependence of the inward spread of activation in isolated twitch muscle fibres of the frog , 1972, The Journal of physiology.

[5]  P. M. Best,et al.  Contractile activation and recovery in skinned frog muscle stimulated by ionic substitution. , 1988, The American journal of physiology.

[6]  A. F. Huxley,et al.  Local activation of striated muscle fibres , 1958 .

[7]  R. Fitts Cellular mechanisms of muscle fatigue. , 1994, Physiological reviews.

[8]  G. Stephenson,et al.  Ion Movements in Skeletal Muscle in Relation to the Activation of Contraction , 1986 .

[9]  M. W. Fryer,et al.  Actions of caffeine on fast‐ and slow‐twitch muscles of the rat. , 1989, The Journal of physiology.

[10]  A. Dulhunty The voltage-activation of contraction in skeletal muscle. , 1992, Progress in biophysics and molecular biology.

[11]  R. J. Podolsky,et al.  Depolarization of the Internal Membrane System in the Activation of Frog Skeletal Muscle , 1967, The Journal of general physiology.

[12]  G. Lamb,et al.  Effects of intracellular pH and [Mg2+] on excitation‐contraction coupling in skeletal muscle fibres of the rat. , 1994, The Journal of physiology.

[13]  G. Lamb,et al.  Calcium release in skinned muscle fibres of the toad by transverse tubule depolarization or by direct stimulation. , 1990, The Journal of physiology.

[14]  L L Costantin,et al.  The Role of Sodium Current in the Radial Spread of Contraction in Frog Muscle Fibers , 1970, The Journal of general physiology.

[15]  P. Junankar,et al.  Raised intracellular [Ca2+] abolishes excitation‐contraction coupling in skeletal muscle fibres of rat and toad. , 1995, The Journal of physiology.

[16]  H. Shuman,et al.  Composition of vacuoles and sarcoplasmic reticulum in fatigued muscle: electron probe analysis. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Lee D. Peachey,et al.  THE SARCOPLASMIC RETICULUM AND TRANSVERSE TUBULES OF THE FROG'S SARTORIUS , 1965, The Journal of cell biology.

[18]  P A Pappone,et al.  Voltage‐clamp experiments in normal and denervated mammalian skeletal muscle fibres. , 1980, The Journal of physiology.

[19]  E. W. Stephenson Excitation of skinned muscle fibers by imposed ion gradients. I. Stimulation of 45Ca efflux at constant [K][Cl] product , 1985, The Journal of general physiology.

[20]  W. Chandler,et al.  Effects of glycerol treatment and maintained depolarization on charge movement in skeletal muscle. , 1976, The Journal of physiology.

[21]  A. Gilai,et al.  Radial propagation of muscle action potential along the tubular system examined by potential-sensitive dyes , 1980, The Journal of general physiology.

[22]  A. Hodgkin,et al.  Potassium contractures in single muscle fibres , 1960, The Journal of physiology.

[23]  A. Huxley Local activation of striated muscle fibres , 1958, Pflüger's Archiv für die gesamte Physiologie des Menschen und der Tiere.

[24]  H. Westerblad,et al.  Muscle cell function during prolonged activity: cellular mechanisms of fatigue , 1995, Experimental physiology.