Kinetic effects of fiber type on the two subcomponents of the Huxley-Simmons phase 2 in muscle

被引:17
作者
Davis, JS [1 ]
Epstein, ND [1 ]
机构
[1] NHLBI, Mol Physiol Sect, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0006-3495(03)74483-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The Huxley-Simmons phase 2 controls the kinetics of the first stages of tension recovery after a step-change in fiber length and is considered intimately associated with tension generation. It had been shown that phase 2 is comprised of two distinct unrelated phases. This is confirmed here by showing that the properties of phase 2(fast) are independent of fiber type, whereas those of phase 2(slow) are fiber type dependent. Phase 2fast has a rate of 1000-2000 s(-1) and is temperature insensitive (Q(10) similar to 1.16) in fast, medium, and slow speed fibers. Regardless of fiber type and temperature, the amplitude of phase 2(fast) is half (similar to0.46) that of phase 1 (fiber instantaneous stiffness). Consequently, fiber compliance (cross-bridge and thick/thin filament) appears to be the common source of both phase 1 elasticity and phase 2(fast) viscoelasticity. In fast fibers, stiffness increases in direct proportion to tension from an extrapolated positive origin at zero tension. The simplest explanation is that tension generation can be approximated by two-state transition from attached preforce generating (moderate stiffness) to attached force generating (high stiffness) states. Phase 2(slow) is quite different, progressively slowing in concert with fiber type. An interesting interpretation of the amplitude and rate data is that reverse coupling of phase 2(slow) back to Pi release and ATP hydrolysis appears absent in fast fibers, detectable in medium speed fibers, and marked in slow fibers contracting isometrically. Contracting slow and heart muscles stretched under load could employ this enhanced reversibility of the cross-bridge cycle as a mechanism to conserve energy.
引用
收藏
页码:390 / 401
页数:12
相关论文
共 51 条
[1]
TEMPERATURE AND AMPLITUDE DEPENDENCE OF TENSION TRANSIENTS IN GLYCERINATED SKELETAL AND INSECT FIBRILLAR MUSCLE [J].
ABBOTT, RH ;
STEIGER, GJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1977, 266 (01) :13-42
[2]
Bagni MA, 1998, J MUSCLE RES CELL M, V19, P33
[3]
Muscle force is generated by myosin heads stereospecifically attached to actin [J].
Bershitsky, SY ;
Tsaturyan, AK ;
Bershitskaya, ON ;
Mashanov, GI ;
Brown, P ;
Burns, R ;
Ferenczi, MA .
NATURE, 1997, 388 (6638) :186-190
[4]
TECHNIQUE FOR STABILIZING THE STRIATION PATTERN IN MAXIMALLY CALCIUM-ACTIVATED SKINNED RABBIT PSOAS FIBERS [J].
BRENNER, B .
BIOPHYSICAL JOURNAL, 1983, 41 (01) :99-102
[5]
Measurement of nucleotide release kinetics in single skeletal muscle myofibrils during isometric and isovelocity contractions using fluorescence microscopy [J].
Chaen, S ;
Shirakawa, I ;
Bagshaw, CR ;
Sugi, H .
BIOPHYSICAL JOURNAL, 1997, 73 (04) :2033-2042
[6]
Chaen S, 1998, ADV EXP MED BIOL, V453, P569
[7]
Actomyosin interaction in striated muscle [J].
Cooke, R .
PHYSIOLOGICAL REVIEWS, 1997, 77 (03) :671-697
[8]
REVERSAL OF THE CROSS-BRIDGE FORCE-GENERATING TRANSITION BY PHOTOGENERATION OF PHOSPHATE IN RABBIT PSOAS MUSCLE-FIBERS [J].
DANTZIG, JA ;
GOLDMAN, YE ;
MILLAR, NC ;
LACKTIS, J ;
HOMSHER, E .
JOURNAL OF PHYSIOLOGY-LONDON, 1992, 451 :247-278
[9]
Davidson D L, 1993, Seizure, V2, P1, DOI 10.1016/S1059-1311(05)80095-0
[10]
DAVIS J S, 1991, Biophysical Journal, V59, p35A