A new integrative method successfully quantifies total Ca2+ handling and futile Ca2+ cycling in a canine model of failing hearts.
Answers are grounded in this paper and cite their sources.
Enables precise Ca2+ handling quantification in failing canine hearts; extends integrative methods but leaves open human translation and clinical relevance.
Ca2+ handling in excitation-contraction coupling requires considerable O2 consumption (VO2) in cardiac contraction. We have developed an integrative method to quantify total Ca2+ handling in normal hearts. However, its direct application to failing hearts, where futile Ca2+ cycling via the Ca2+-leaky sarcoplasmic reticulum (SR) required an increased Ca2+ handling VO2, was not legitimate. To quantify total Ca2+ handling even in such failing hearts, we combined futile Ca2+ cycling with Ca2+ handling VO2 and the internal Ca2+ recirculation fraction via the SR. We applied this method to the canine heart mechanoenergetics before and after intracoronary ryanodine at nanomolar concentrations. We found that total Ca2+ handling per beat was halved after the ryanodine treatment from approximately 60 micromol/kg left ventricle before ryanodine. We also found that futile Ca2+ cycling via the SR increased to >1 cycle/beat after ryanodine from presumably zero before ryanodine. These results support the applicability of the present method to the failing hearts with futile Ca2+ cycling via the SR.
No takes yet. Share an insight, caveat, or question.
Shimizu et al. (1998) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: