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Recieved from the Department of Anesthesiology, University of Alabama School of Medicine, Birmingham, Alabama.
Abstract
The effects of fentanyl, nitrous oxide, and their combination on myocardial contractility were investigated in the papillary muscle preparation perfused by a donor dog. With a conscious donor, fentanyl infused directly into the arterial blood perfusing the papillary muscle produced a dose-related depression of developed tension. However, blood concentrations of fentanyl required to obtain the depression were in the range of 30–120 µg/ml. The ED50 for fentanyl for suppression of papillary muscle contractility was 89 ± 9 µg/ml. When the donor dog was given nitrous oxide (N2O,80% and O2,20%), the developed tension of the papillary muscle decreased 25 ± 5%. Fentanyl administered during nitrous oxide anesthesia caused a decrease in developed tension that was not significantly different from that obtained without N2O anesthesia (18 ± 4% vs 13 ± 4% for 30 µg/ml, and 61 ± 5% vs 58 ± 4% for 100 µg/ml). The results suggest that fentanyl produces a direct negative inotropic effect only in concentrations that are 2–3 orders of magnitude higher than its blood concentrations in fentanyl-induced anesthesia. When fentanyl and nitrous oxide are used together their interaction is not significantly different from additive.
Key Words: ANESTHESIA, intravenous—fentanyl ANESTHETICS, gases—nitrous oxide HEART—contractility
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