Calcium-Induced Inotropy Is in Part Mediated by Protein Kinase C

Protein kinase C (PKC) is an ubiquitous regulatory enzyme with dense myocardial distribution and activity; however, its physiologic relevance to myocardial function remains poorly understood. Although endogenous Ca2+is a potent stimulus of PKC isoforms α and β (cPKCs) it remains unknown whether exogenous Ca2+activates these PKC isoforms, and if so, whether PKC plays any role in Ca2+-induced myocardial inotropy. To study this, ventricular sections from isolated rat hearts, with and without Ca2+-induced inotropy (CaCl2, 0.5 mMcoronary concentration × 2 min), were probed for cPKC isoform translocation using immunofluorescence in order to determine if exogenous Ca2+indeed activates cPKCs. We further examined the effects of exogenous Ca2+, with and without concurrent PKC inhibition (chelerythrine, 20 μMcoronary concentration × 2 min), on fundamental physiologic parameters of myocardial developed pressure (DP), dP/dt, and coronary flow (CF) in the isolated rat heart to determine if Ca2+-induced inotropy involves PKC. Results indicated that exogenous Ca2+results in translocation of PKC α from the cytoplasm to the sarcolemma and intercalated discs, as well as the translocation of PKC β from the perinuclear to the intranuclear compartment. This dose of exogenous Ca2+resulted in myocardial inotropy as determined by DP, dP/dt, and CF. Furthermore, myocardial inotropy was attenuated with concurrent inhibition of PKC activity. These findings link the physiologic effects of exogenous Ca2+to PKC, providing a better understanding of the physiologic mechanism of Ca2+-induced inotropy.