MIDAZOLAM IS A SAFE AGENT BY COMPARISON WITH THIOPENTONE ON ARRHYTHMIAS IN ISCHEMIA AND REPERFUSION CONDITIONS IN ISOLATED-PERFUSED RAT HEARTS

Citation
O. Suzer et al., MIDAZOLAM IS A SAFE AGENT BY COMPARISON WITH THIOPENTONE ON ARRHYTHMIAS IN ISCHEMIA AND REPERFUSION CONDITIONS IN ISOLATED-PERFUSED RAT HEARTS, Pharmacological research, 37(6), 1998, pp. 461-468
Citations number
21
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
10436618
Volume
37
Issue
6
Year of publication
1998
Pages
461 - 468
Database
ISI
SICI code
1043-6618(1998)37:6<461:MIASAB>2.0.ZU;2-U
Abstract
Arrhythmia due to ischaemia and/or reperfusion is an important problem , especially in open heart surgery and for patients with ischaemic hea rt diseases undergoing non-cardiac surgery. This experimental study is planned to evaluate the effects of midazolam on ischaemia and/or repe rfusion-induced arrhythmias by comparison with thiopentone in two sets of experiments (n = 20 for every group). In total ischaemia-reperfusi on experiments, hearts were perfused in constant pressure conditions. In the control group, after a stabilisation period, perfusion was tota lly stopped for 30 min and the hearts were reperfused for 10 min. For the experimental groups, hearts were pretreated for 5 min with either 10(-6) mol l(-1) midazolam or 10(-5) mol l(-1) thiopentone before tota l ischaemia and reperfused for 10 min with the same concentrations of the drugs. In low-flow ischaemia-reperfusion experiments, hearts were perfused at a constant flow of 10 ml g(-1) heart per min initially. In the control group, after a stabilisation period, perfusion rate was d ecreased successively 1 ml g(-1) heart per min for 10 min (mild ischae mia) and to 0.2 ml g(-1) heart per min for another 10 min (severe isch aemia). The ischaemic hearts were then reperfused for an additional 10 min at a flow rate of 10 ml g(-1) heart per min. Electrogram recordin gs were evaluated before ischaemia and at the 5th and 10th min of mild ischaemia, severe ischaemia and reperfusion. Midazolam, 10(-6) mol l( -1), or thiopentone, 10(-5) mol l(-1), were added to the perfusion sol ution in the midazolam and thiopentone groups, respectively. In these two groups, hearts were perfused according to perfusion rates mentione d above in the control group. As a commonly used i.v. anaesthetic, thi opentone was arrhythmogenic for hearts exposed to ischaemia-reperfusio n by increasing ventricular premature beat (% incidences for control, midazolam and thiopental groups in the 10th min of reperfusion were 25 , 15 and 65 in total ischaemia-reperfusion experiments, P < 0.01) and ventricular tachycardia (respective % incidences were 0, 5, 25, P < 0. 05) incidences, but in our experiments we found out that the new agent midazolam does not have more arrhythmia incidence than the respective control group in any criteria evaluated. None of the agents exerted a trioventricular conductance abnormalities. So we conclude that midazol am is a safe agent for ischaemic hearts and might also be antiarrhythm ic and the mechanism of action of this effect remains to be further in vestigated. (C) 1998 The Italian Pharmacological Society.