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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Callahan, Damien M. Bedrin, Nicholas G. Subramanian, Meenakumari Berking, James Ades, Philip A. Toth, Michael J. Miller, Mark S. |
| Description | Author Affiliation: Callahan DM ( Department of Medicine, University of Vermont, Burlington, Vermont); Bedrin NG ( Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont.); Subramanian M ( Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont.); Berking J ( Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont.); Ades PA ( Department of Medicine, University of Vermont, Burlington, Vermont); Toth MJ ( Department of Medicine, University of Vermont, Burlington, Vermont); Miller MS ( Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont Mark.Miller@uvm.edu.) |
| Abstract | Age-related loss of skeletal muscle mass and function is implicated in the development of disease and physical disability. However, little is known about how age affects skeletal muscle structure at the cellular and ultrastructural levels or how such alterations impact function. Thus we examined skeletal muscle structure at the tissue, cellular, and myofibrillar levels in young (21-35 yr) and older (65-75 yr) male and female volunteers, matched for habitual physical activity level. Older adults had smaller whole muscle tissue cross-sectional areas (CSAs) and mass. At the cellular level, older adults had reduced CSAs in myosin heavy chain II (MHC II) fibers, with no differences in MHC I fibers. In MHC II fibers, older men tended to have fewer fibers with large CSAs, while older women showed reduced fiber size across the CSA range. Older adults showed a decrease in intermyofibrillar mitochondrial size; however, the age effect was driven primarily by women (i.e., age by sex interaction effect). Mitochondrial size was inversely and directly related to isometric tension and myosin-actin cross-bridge kinetics, respectively. Notably, there were no intermyofibrillar or subsarcolemmal mitochondrial fractional content or myofilament ultrastructural differences in the activity-matched young and older adults. Collectively, our results indicate age-related reductions in whole muscle size do not vary by sex. However, age-related structural alterations at the cellular and subcellular levels are different between the sexes and may contribute to different functional phenotypes in ways that modulate sex-specific reductions in physical capacity with age. |
| File Format | HTM / HTML |
| ISSN | 87507587 |
| e-ISSN | 15221601 |
| DOI | 10.1152/japplphysiol.01362.2013 |
| Journal | Journal of Applied Physiology |
| Issue Number | 12 |
| Volume Number | 116 |
| Language | English |
| Publisher | American Physiological Society |
| Publisher Date | 2014-06-15 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Discipline Physiology Aging Physiology Mitochondria Muscle Fibers, Skeletal Actins Metabolism Motor Activity Myosin Heavy Chains Research Support, N.i.h., Extramural |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physiology Physiology (medical) Sports Science |
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