Aging impairs regulation of ryanodine receptors from extensor digitorum longus but not soleus muscles

Muscle Nerve. 2018 Jun;57(6):1022-1025. doi: 10.1002/mus.26063. Epub 2018 Jan 30.

Abstract

Introduction: Because impaired excitation-contraction coupling and reduced sarcoplasmic reticulum (SR) Ca2+ release may contribute to the age-associated decline in skeletal muscle strength, we investigated the effect of aging on regulation of the skeletal muscle isoform of the ryanodine receptor (RyR1) by physiological channel ligands.

Methods: [3 H]Ryanodine binding to membranes from 8- and 26-month-old Fischer 344 extensor digitorum longus (EDL) and soleus muscles was used to investigate the effects of age on RyR1 modulation by Ca2+ and calmodulin (CaM).

Results: Aging reduced maximal Ca2+ -stimulated binding to EDL membranes. In 0.3 μM Ca2+ , age reduced binding and CaM increased binding to EDL membranes. In 300 μM Ca2+ , CaM reduced binding, but the age effect was not significant. Aging did not affect Ca2+ or CaM regulation of soleus RyR1.

Discussion: In aged fast-twitch muscle, impaired RyR1 Ca2+ regulation may contribute to lower SR Ca2+ release and reduced muscle function. Muscle Nerve 57: 1022-1025, 2018.

Keywords: aging; calcium; calmodulin; excitation-contraction coupling; ryanodine receptor; sarcoplasmic reticulum; skeletal muscle.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aging / metabolism*
  • Animals
  • Calcium Signaling / physiology*
  • Excitation Contraction Coupling / physiology*
  • Male
  • Muscle, Skeletal / metabolism*
  • Rats
  • Rats, Inbred F344
  • Ryanodine Receptor Calcium Release Channel / metabolism*
  • Sarcoplasmic Reticulum / metabolism

Substances

  • Ryanodine Receptor Calcium Release Channel