Measurement of calcium and movement in heart cells

Methods Mol Biol. 2005:312:261-8. doi: 10.1385/1-59259-949-4:261.

Abstract

Preparations of calcium-tolerant cardiac myocytes for studies on intracellular calcium ([Ca(2+)](i)) signaling and contraction have been difficult owing to the susceptibility of these cells to the enzymatic digestion process. This often leads to the cells acquiring a bricklike contracted shape with a granular cytoplasm and membrane blebbing. A successful preparation results in single myocytes that do not show spontaneous contractions and that remain relaxed in Ca(2+)-containing buffers, indicating that the sarcolemmal membrane was not damaged during enzymatic digestion and led to membrane depolarization.

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Signaling
  • Fura-2 / analogs & derivatives*
  • Fura-2 / metabolism
  • Myocardial Contraction
  • Myocardium / cytology
  • Myocardium / metabolism
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / metabolism*
  • Rats
  • Rats, Wistar
  • Sarcolemma / metabolism

Substances

  • fura-2-am
  • Calcium
  • Fura-2