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*Department of Anesthesiology, Sapporo Medical University School of Medicine, Sapporo, Japan; and
Department of Anesthesia, Hokkaido Keiaikai Minami 1-jyo Hospital, Sapporo, Japan
Address correspondence and reprint requests to Yuri Nakae, MD, PhD, Department of Anesthesiology, Medical College of Wisconsin, 8701 Watertown Plank Rd., Milwaukee, WI 53226-0509. Address e-mail to ynakae{at}mcw.edu
Isoproterenol is often required to treat acute left ventricular dysfunction during separation from cardiopulmonary bypass for cardiac surgery. We hypothesized that heart rate and intracellular Ca2+ concentration ([Ca2+]i) homeostasis may be important factors when isoproterenol improves the cardiac function during hypothermia. Accordingly, we investigated the effect of isoproterenol on the cardiac functional variables, [Ca2+]i, and myofilament Ca2+ sensitivity under spontaneous beating during hypothermia. Intact guinea pig hearts were perfused with a modified Krebs-Ringer solution (baseline) and Krebs-Ringer solution containing isoproterenol (1 nM) at 37°C, 32°C, and 27°C while all cardiac variables and [Ca2+]i were recorded. Isoproterenol increased developed left ventricular pressure (LVP), maximum rate of increase in LVP, and coronary inflow at 27°C, and it also increased heart rate and maximum rate of decrease in LVP at each temperature (P < 0.05). Isoproterenol produced a leftward shift of the curve of developed LVP as a function of available [Ca2+]i at 32°C and 27°C (P < 0.05), without changing available [Ca2+]i. Isoproterenol improves the cardiac function, especially systolic ventricular function, by enhancement of myofilament Ca2+ sensitivity under spontaneous beating during hypothermia in intact guinea pig hearts.
IMPLICATIONS: Enhancement of myofilament Ca2+ sensitivity is involved in the improvement of cardiac function by isoproterenol under spontaneous beating during hypothermia.
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