Diacylglycerol enhances systolic Ca2+ transients, suggesting excitation-contraction coupling is a key target of diacylglycerol-protein kinase C signaling in the myocardium.
Diacylglycerol has been hypothesized to mediate the positive inotropic response of myocardium to the alpha-adrenergic agonists angiotensin II and endothelin. The mechanism of action of diacylglycerol was examined here in adult rat ventricular myocytes by releasing dioctanoylglycerol (diC8) intracellularly from a caged compound while monitoring Ca2+ transients and pH with fluorescent indicators. DiC8 caused a three- to fourfold increase in twitch amplitude and a twofold increase in the systolic Ca2+ transient. No other parameter was consistently influenced by diC8, including the kinetics of Ca2+ cycling, the Ca2+ content of the sarcoplasmic reticulum, or the myofilament Ca2+ sensitivity. DiC8 also had no detectable effect on intracellular pH or Na+/H+ antiport activity. Consistent with this finding, the Na+/H+ exchange inhibitor N-ethylisopropyl amiloride was without effect on the positive inotropic response to diC8. The marked enhancement of systolic Ca2+ by diC8 suggests that the process of excitation-contraction coupling is an important and possibly preferred target of diacylglycerol-protein kinase C signaling in myocardium.
Pi et al. (1998) studied this question.