Myocyte contractility can be maintained by storing cells with the myosin ATPase inhibitor 2,3 butanedione monoxime

Charles S. Chung, Charles Mechas, Kenneth S. Campbell

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Isolated intact myocytes can be used to investigate contractile mechanisms and to screen new therapeutic compounds. These experiments typically require euthanizing an animal and isolating fresh cells each day or analyzing cultured myocytes, which quickly lose their rod-shaped morphology. Recent data suggest that the viability of canine myocytes can be prolonged using low temperature and N-benzyl-p-toluene sulfonamide (an inhibitor of skeletal myosin ATPase). We performed similar studies in rat myocytes in order to test whether the cardiac myosin ATPase inhibitors 2,3-Butanedione monoxime (BDM) and blebbistatin help to maintain cell-level function over multiple days. Myocytes were isolated from rats and separated into batches that were stored at 4°C in a HEPES-buffered solution that contained 0.5 mmol L-1 Ca2+ and (1) no myosin ATPase inhibitors; (2) 10 mmol L-1 BDM; or (3) 3 μmol L-1 blebbistatin. Functional viability of myocytes was assessed up to 3 days after the isolation by measuring calcium transients and unloaded shortening profiles induced by electrical stimuli in inhibitor-free Tyrode’s solution. Cells stored without myosin ATPase inhibitors had altered morphology (fewer rod-shaped cells, shorter diastolic sarcomere lengths, and membrane blebbing) and were not viable for contractile assays after 24 h. Cells stored in BDM maintained morphology and contractile function for 48 h. Storage in blebbistatin maintained cell morphology for 72 h but inhibited contractility. These data show that storing cells with myosin ATPase inhibitors can extend the viability of myocytes that will be used for functional assays. This may help to refine and reduce the use of animals in experiments.

Original languageEnglish
Article numbere12445
JournalPhysiological Reports
Volume3
Issue number6
DOIs
StatePublished - 2015

Bibliographical note

Funding Information:
This study was supported by the American Heart Association (Scientist Development Grant 14SDG20100063) to CSC and the National Institutes of Health (R01 HL090749) to KSC and CTSA UL1TR000117.

Publisher Copyright:
© 2015 The Authors.

Keywords

  • 3-Butanedione monoxime)
  • BDM (2
  • Blebbistatin
  • Calcium
  • Cardiomyocyte
  • Crossbridge
  • Sarcomere

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)

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