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Exp Gerontol. 2014 Feb;50:40-4. doi: 10.1016/j.exger.2013.11.018. Epub 2013 Dec 4.

Weakness, SR function and stress in gastrocnemius muscles of aged male rats.

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  • 1Division of Physical Therapy, Ohio University, Athens, OH, USA; Ohio Musculoskeletal and Neurological Institute (OMNI), Heritage College of Osteopathic Medicine, Athens, OH, USA. Electronic address: russd@ohio.edu.
  • 2Division of Physical Therapy, Ohio University, Athens, OH, USA.

Abstract

Aging is associated with a decline in muscle force that exceeds loss of muscle mass, suggesting that factors other than sarcopenia affect age-related muscle weakness. Here, we investigate in situ muscle force and sarcoplasmic reticulum (SR) properties in gastrocnemius muscles of adult (6-8 months) and aged (24 months) rats. Despite minimal loss of muscle mass, peak tetanic force was significantly reduced (-28%) in aged muscles. Adjusting for differences in muscle cross-sectional area mitigated the age difference (-23%), but it remained significant. The SR calcium release function was also impaired (-17%) with aging, although calcium uptake was not, and SR-associated glycogen increased (+30%) with aging. Western blotting revealed age related increases in Grp78, serinepalmitoyltransferase and neutral sphingomyelinase, suggesting that age increased the stress response and ceramide metabolism in the SR. In contrast Parkin, a protein associated with autophagic signaling, was reduced in the aged SR. These findings are consistent with a hypothesis that age-related impairments of the SR, possibly due to impaired autophagy and/or altered membrane metabolism, contribute to age-related muscle weakness, independent of changes in muscle mass.

Copyright © 2013 Elsevier Inc. All rights reserved.

KEYWORDS:

78kD glucose regulated protein; Autophagy; CSA; Calcium; Ceramide; ER; E–C coupling; GP; Grp78; MHC; Parkin; SPT; SR; Sarcopenia; aSMase; acid sphingomyelinase; cross-sectional area; endoplasmic reticulum; excitation–contraction coupling; glycogen phosphorylase; l(o); myosin heavy chain; nSMase; neutral sphingomyelinase; optimal length; sarcoplasmic reticulum; serine palmitoyltransferase

PMID:
24316040
[PubMed - indexed for MEDLINE]
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