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
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.