Differential effects of fentanyl and morphine on intracellular Ca2+ transients and contraction in rat ventricular myocytes

Background: Our objective was to elucidate the direct effects of fentanyl a nd morphine on cardiac excitation-contraction coupling using individual, fi eld-stimulated rat ventricular myocytes, Methods: Freshly isolated myocytes were loaded with fura-2 and field stimul ated (0.3 Hz) at 28 degrees C. Amplitude and timing of intracellular Ca2+ c oncentration (at a 340:380 ratio) and myocyte shortening (video edge detect ion) were monitored simultaneously in individual cells. Real time Ca2+ upta ke into isolated sarcoplasmic reticulum vesicles was measured using fura-2 free acid in the extravesicular compartment, Results: The authors studied 120 cells from 30 rat hearts. Fentanyl (30-1,0 00 nM) caused dose-dependent decreases in peak intracellular Ca2+ concentra tion and shortening, whereas morphine (3-100 mu M) decreased shortening wit hout a concomitant decrease in the Ca2+ transient. Fentanyl prolonged the t ime to peak and to 50% recovery for shortening and the Ca2+ transient, wher eas morphine only prolonged the timing parameters for shortening. Morphine (100 mu M) but not fentanyl(l mu M), decreased the amount of Ca2+ released from Intracellular stores in response to caffeine in intact cells, and it i nhibited the rate of Ca2+ uptake in isolated sarcoplasmic reticulum vesicle s. Fentanyl and morphine both caused a downward shift in the dose-response curve to extracellular Ca2+ for shortening, with no concomitant effect on t he Ca2+ transient. Conclusions: Fentanyl and Morphine directly depress cardiac excitation-cont raction coupling at the cellular level. Fentanyl depresses myocardial contr actility by decreasing the availability of intracellular Ca2+ and myofilame nt Ca2+ sensitivity. In contrast, morphine depresses myocardial contractili ty primarily by decreasing myofilament Ca2+ sensitivity.