Calcium ATPase in the sarcoplasmic reticulum of muscle from normal and malignant hyperthermia susceptible pigs

Neurosci Lett. 1991 Oct 14;131(2):187-92. doi: 10.1016/0304-3940(91)90610-6.

Abstract

The density of Mg(2+)-dependent Ca2+ ATPase in the terminal cisternae of pig skeletal muscle fibers was investigated to discover whether a reduction in Ca2+ ATPase content impairs Ca2+ sequestration and contributes to the elevated myoplasmic Ca2+ concentration in malignant hyperthermia. Unexpectedly, immunogold electron microscopy showed an increase in Ca2+ ATPase, while densitometry of SDS-polyacrylamide gels suggested that the Ca2+ ATPase content of terminal cisternae vesicles did not change. The affinity of Ca2+ ATPase in vesicles for our monoclonal antibody was not altered. We suggest that the availability of antigenic sites in malignant hyperthermia increases after processing for electron microscopy, perhaps as a consequence of altered sarcoplasmic reticulum membrane properties.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / analysis
  • Ca(2+) Mg(2+)-ATPase / metabolism
  • Calcium / metabolism
  • Calcium-Transporting ATPases / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Immunohistochemistry
  • Malignant Hyperthermia / enzymology*
  • Microscopy, Immunoelectron
  • Muscles / enzymology*
  • Muscles / ultrastructure
  • Sarcoplasmic Reticulum / enzymology*
  • Swine

Substances

  • Antibodies, Monoclonal
  • Ca(2+) Mg(2+)-ATPase
  • Calcium-Transporting ATPases
  • Calcium