Mechanism of specific force deficit in the senescent rat diaphragm

Respir Physiol. 1997 Feb;107(2):149-55. doi: 10.1016/s0034-5687(96)02509-1.

Abstract

Aging is associated with a decline in the maximal in vitro specific force in the rat costal diaphragm. The purpose of this study was to determine if this force deficit is associated with a decrease in the concentration of myofibrillar protein in diaphragm fibers of senescent rats. Isometric twitch and tetanic contractile properties were measured on diaphragm strips from young adult (9-month-old: n = 12) and senescent (26-month-old: n = 13) male specific pathogen free-barrier protected Fischer 344 rats. Maximal tetanic force (Po) normalized to the cross-sectional area (CSA) of the in vitro diaphragm strips was 16.4% lower in the senescent diaphragms (21.03 +/- 0.4 N/cm2) compared to the young adult (25.16 +/- 0.5 N/cm2) (p < 0.001). Diaphragm water content was significantly higher in the senescent group (75.9% of total wet mass) compared to the young adult (72.1% of total wet mass, p < 0.05). Subtracting the contribution of water from the CSA of the diaphragm strips significantly reduced (p < 0.05) the senescent specific Po deficit (from -16.4 to -6.4%). Further, correcting Po for the contribution of myofibrillar protein to CSA resulted in no age group differences in specific force. These data indicate that the age-related decline in diaphragm in vitro maximal specific Po can be explained by an age-related increase in the water content of the diaphragm muscle. Future experiments are necessary to determine the mechanism(s) responsible for this observation.

MeSH terms

  • Aging / physiology*
  • Animals
  • Body Water / physiology
  • Body Weight / physiology
  • Carrier Proteins
  • Diaphragm / anatomy & histology
  • Diaphragm / metabolism
  • Diaphragm / physiology*
  • In Vitro Techniques
  • Isometric Contraction / physiology
  • Male
  • Muscle Contraction / physiology
  • Muscle Proteins / metabolism
  • Rats
  • Rats, Inbred F344

Substances

  • Carrier Proteins
  • Muscle Proteins
  • myosin-binding protein C