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J Appl Physiol 90: 380-388, 2001;
8750-7587/01 $5.00
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Vol. 90, Issue 1, 380-388, January 2001

HIGHLIGHTED TOPICS
Plasticity in Skeletal, Cardiac, and Smooth Muscle
Selected Contribution: Mechanisms underlying increased force generation by rat diaphragm muscle fibers during development

Paige C. Geiger1,2, Mark J. Cody1, Rebecca L. Macken1, Megan E. Bayrd1, Yun-Hua Fang1, and Gary C. Sieck1,2

Departments of Anesthesiology and 1 Physiology and Biophysics,2  Mayo Clinic and Foundation, Rochester, Minnesota 55905

It has been found that maximum specific force (Fmax; force per cross-sectional area) of rat diaphragm muscle doubles from birth to 84 days (adult). We hypothesize that this developmental change in Fmax 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 (MHCslow and MHCneo, 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 MHCslow and coexpressing MHCneo produced less force than fibers expressing fast MHC isoforms. We conclude that lower force per cross bridge in fibers expressing MHCslow and MHCneo contributes to the lower Fmax seen in early postnatal development.

postnatal development; maximum specific force; myosin heavy chain content; force per cross bridge; single fibers


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