Mechanisms underlying increased force generation by rat diaphragm muscle fibers during development

被引:46
作者
Geiger, PC
Cody, MJ
Macken, RL
Bayrd, ME
Fang, YH
Sieck, GC
机构
[1] Mayo Clin & Mayo Fdn, Dept Anesthesiol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Physiol & Biophys, Rochester, MN 55905 USA
关键词
postnatal development; maximum specific force; myosin heavy chain content; force per cross bridge; single fibers;
D O I
10.1152/jappl.2001.90.1.380
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
It has been found that maximum specific force (F(max); force per cross-sectional area) of rat diaphragm muscle doubles from birth to 84 days (adult). We hypothesize that this developmental change in F(max) reflects an increase in myosin heavy chain (MHC) content per half-sarcomere (an estimate of the number of cross bridges in parallel) and/or a greater force per cross bridge in fibers expressing fast MHC isoforms compared with slow and neonatal MHC isoforms (MHC(slow) and MHC(neo), respectively). Single Triton 100-X-permeabilized fibers were activated at a pCa of 4.0. MHC isoform expression was determined by SDS-PAGE. MHC content per half-sarcomere was determined by densitometric analysis and comparison to a standard curve of known MHC concentrations. MHC content per half-sarcomere progressively increased during early postnatal development. When normalized for MHC content per half-sarcomere, fibers expressing MHC(slow) and coexpressing MHC(neo) produced less force than fibers expressing fast MHC isoforms. We conclude that lower force per cross bridge in fibers expressing MHC(slow) and MHC(neo) contributes to the lower F(max) seen in early postnatal development.
引用
收藏
页码:380 / 388
页数:9
相关论文
共 47 条
[1]   FORCE-VELOCITY RELATIONS AND MYOSIN HEAVY-CHAIN ISOFORM COMPOSITIONS OF SKINNED FIBERS FROM RAT SKELETAL-MUSCLE [J].
BOTTINELLI, R ;
SCHIAFFINO, S ;
REGGIANI, C .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 437 :655-672
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   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]   Right ventricular contractile protein function in rats with left ventricular myocardial infarction [J].
deTombe, PP ;
Wannenburg, T ;
Fan, DS ;
Little, WC .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (01) :H73-H79
[6]   MECHANICAL-PROPERTIES OF SKINNED SINGLE FIBERS OF IDENTIFIED TYPES FROM RAT DIAPHRAGM [J].
EDDINGER, TJ ;
MOSS, RL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (02) :C210-C218
[7]  
FABIATO A, 1979, J PHYSIOL-PARIS, V75, P463
[8]   THE DETERMINANTS OF SKELETAL-MUSCLE FORCE AND POWER - THEIR ADAPTABILITY WITH CHANGES IN ACTIVITY PATTERN [J].
FITTS, RH ;
MCDONALD, KS ;
SCHLUTER, JM .
JOURNAL OF BIOMECHANICS, 1991, 24 :111-122
[9]   Force-calcium relationship depends on myosin heavy chain and troponin isoforms in rat diaphragm muscle fibers [J].
Geiger, PC ;
Cody, MJ ;
Sieck, GC .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 87 (05) :1894-1900
[10]   Maximum specific force depends on myosin heavy chain content in rat diaphragm muscle fibers [J].
Geiger, PC ;
Cody, MJ ;
Macken, RL ;
Sieck, GC .
JOURNAL OF APPLIED PHYSIOLOGY, 2000, 89 (02) :695-703