Successive contractile periods activate mitochondria at the onset of contractions in intact rat cardiac trabeculae.

The rate of oxidative phosphorylation depends on the contractile activity of the heart. Cardiac mitochondria' oxidative phosphorylation is determined by free ADP concentration, mitochondrial Ca2+ accumulation, mitochondria' enzyme activities, and Krebs cycle intermediates. The purpose of the present study was to examine the factors that limit oxidative phosphorylation upon rapid changes in contractile activity in cardiac muscle. We tested the hypotheses that prior contractile performance enhances the changes in NAD(P)H and FAD concentration upon an increase in contractile activity and that this mitochondrial "priming" depends on pyruvate dehydmgenase activity. Intact rat cardiac trabeculae were electrically stimulated at 0.5 Hz for at least 30 min. Thereafter, two equal bouts at elevated stimulation frequency of 1, 2, or 3 Hz were applied for 3 min with 3 min of 0.5-Hz stimulation in between. No discernible time delay was observed in the changes in NAD(P)H and FAD fluorescence upon rapid changes in contractile activity. The amplitudes of the rapid changes in fluorescence upon an increase in stimulation frequency (the on-transients) were smaller than upon a decrease in stimulation frequency (the off-transients). A first bout in glucose-containing superfusion solution resulted, during the second bout, in an increase in the amplitudes of the on-transients, but the off-transients remained the same. No such priming effect was observed after addition of 10 mM pyruvate. These results indicate that mitochondria' priming can be observed in cardiac muscle in situ and that pyruvate dehydrogenase activity is critically involved in the mitochondria' adaptation to increases in contractile performance. NEW & NOTEWORTHY Mitochondria' respiration increases with increased cardiac contractile activity. Similar to mitochondria' "priming" in skeletal muscle, we hypothesized that cardiac mitochondria' activity is altered upon successive bouts of contractions and depends on pyruvate dehydrogenase activity. We found altered bioenergetics upon repeated contractile periods, indicative of mitochondria' priming in rat myocardium. No effect was seen when pyruvate was added to the perfusate. As such, pyruvate dehydrogenase activity is involved in the mitochondria' adaptation to increased contractile performance.