(6,34 +--0,74 vs 8,40 +--1,13Epinephrine exerts its effects on the heart through adrenergic receptors. Myocardial beta receptors have been considered to be one of the responsible receptors mediating the catecholamine-induced arrhythmias.l"4 Propranolol, a nonselective beta antagonist, l and 1-metoprolol, a selective beta I antagonist, 2 have been shown to prevent epinephrine-induced arrhythmia during halothane anaesthesia. Recent reports 5 have described the existence of both beta 1 and beta 2 adrenoceptors in the heart. 5-7 The effect of selective beta 2 antagonism on the genesis of the arrhythmias is controversial. Sharma, 3 using H 35/25 as a beta 2 antagonist, reported a weak protective effect against halothane-epinephrine arrhythmias and concluded that this action was attributed to its non-specific effect. On the other hand, we s examined the effect of a selective beta 2 antagonist, ICI-118,551, on the genesis of the arrhythmias provoked by various combinations of phenylephrine and isoproterenol, and showed that ICI-118,551 potentiated isoproterenol-induced arrhythmias in the presence of a low CAN J ANAESTH t992 / 39:8 / pp 873-6