Interaction of Halothane with α- and β-Adrenoceptor Stimulations in Rat Myocardium
Open Access
- 1 January 1997
- journal article
- other
- Published by Wolters Kluwer Health in Anesthesiology
- Vol. 86 (1) , 147-159
- https://doi.org/10.1097/00000542-199701000-00019
Abstract
Background: Halothane induces negative inotropic and lusitropic effects in myocardium. It has been suggested that halothane potentiates beta-adrenoceptor stimulation. However, its effects on the inotropic response to alpha-adrenoceptor stimulation and its effects on the lusitropic effects of alpha- and beta-adrenoceptor stimulation are unknown. Methods: The effects of halothane (0.5 and 1 minimum alveolar concentration [MAC]) on the inotropic responses induced by phenylephrine (10(-8) to 10(-4) M) and isoproterenol (10(-8) to 10(-4) M) were studied in rat left ventricular papillary muscles in vitro (in Krebs-Henseleit solution at 29 degrees C, pH 7.40, with 0.5 mM calcium and stimulation frequency at 12 pulses/min). The lusitropic effects were studied in isotonic (R1) and isometric (R2) conditions. Results: One MAC halothane induced a negative inotropic effect (54 +/- 3%, P < 0.05), increased R1 (109 +/- 3%, P < 0.05), and decreased R2 (88 +/- 2%, P < 0.05). In control groups, phenylephrine (137 +/- 7%, P > 0.05) and isoproterenol (162 +/- 6%, P < 0.05) induced a positive inotropic effect. Halothane did not significantly modify the positive inotropic effect of calcium, suggesting that it did not modify the inotropic reserve of papillary muscles. In contrast, 1 MAC halothane enhanced the positive inotropic effects of phenylephrine (237 +/- 19%, P < 0.05) and isoproterenol (205 +/- 11%, P < 0.05). Halothane did not modify the lusitropic effect of phenylephrine under high or low load. In contrast, 1 MAC halothane impaired the positive lusitropic effect of isoproterenol under low load (P < 0.05), whereas it did not modify the positive lusitropic effect of isoproterenol under high load. Conclusions: At clinically relevant concentrations, halothane potentiated the positive inotropic effects of both alpha- and beta-adrenoceptor stimulation. Furthermore, halothane alters the positive lusitropic-effect of beta-adrenoceptor stimulation under low load.Keywords
This publication has 37 references indexed in Scilit:
- Inhibition of Sodium/Calcium Exchange and Calcium Channels of Heart Cells by Volatile AnestheticsAnesthesiology, 1995
- Anesthetic alteration of ryanodine binding by cardiac calcium release channelsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1994
- Activation of the Ca2+ Release Channel of Cardiac Sarcoplasmic Reticulum by Volatile AnestheticsAnesthesiology, 1994
- Halothane and Isoflurane Decrease Calcium Sensitivity and Maximal Force in Human Skinned Cardiac FibersAnesthesiology, 1994
- Volatile Anesthetic Effects on Sarcoplasmic Reticulum Ca Content and Sarcolemmal Ca Flux in Isolated Rat Cardiac Cell SuspensionsAnesthesiology, 1994
- Alteration of Left Ventricular Diastolic Function by Desflurane, Isoflurane, and Halothane in the Chronically Instrumented Dog with Autonomie Nervous System BlockadeAnesthesiology, 1991
- Comparative Effects of Halothane, Enflurane, and Isoflurane at Equipotent Anesthetic Concentrations on Isolated Ventricular Myocardium of the Ferret. I. ContractilityAnesthesiology, 1988
- Comparative Effects of Halothane, Enflurane, and Isoflurane at Equipotent Anesthetic Concentrations on Isolated Ventricular Myocardium of the Ferret. II. RelaxationAnesthesiology, 1988
- Anesthetic Depression of Myocardial ContractilityAnesthesiology, 1987
- Differential Depression of Myocardial Contractility by Halothane and Isoflurane In VitroAnesthesiology, 1986