Circulation, Vol 83, 2076-2082, Copyright © 1991 by American Heart Association
EP Anyukhovsky and MR Rosen
BACKGROUND. Recent advances in adrenergic pharmacology have made possible
the identification of alpha 1-adrenergic receptor subtypes using the
specific blockers chloroethylclonidine and WB 4101. METHODS AND RESULTS. In
the present study, we used these two blockers to determine the mechanisms
responsible for automatic rhythms occurring during simulated ischemia and
reperfusion of isolated canine Purkinje fibers. Experiments were done in
the presence of propranolol to minimize beta-adrenergic contributions to
the rhythms studied. In the control situation, all fibers showed membrane
potentials greater than - 90 mV and normal automatic rhythms. During
simulated ischemia, membrane potential depolarized to the -60 mV range.
Abnormal automaticity was seen in 20% of fibers not treated with
phenylephrine and in 50% of those superfused with 1 x 10(-7) M
phenylephrine. The incidence of abnormal automaticity was reduced to 0% by
WB 4101 (which blocks phosphoinositide metabolic effects of alpha
1-adrenergic stimulation in the heart) and was increased to 90% by
chloroethylclonidine (which blocks Na-K pump-stimulating effects of
alpha-agonists). Moreover, the ischemic fibers were significantly more
hyperpolarized during superfusion with WB 4101 than with
chloroethylclonidine. Triggered activity induced by delayed or early after
depolarizations was not seen in any experiment. CONCLUSIONS. Automatic
arrhythmias induced by alpha 1-adrenergic stimulation during simulated
ischemia may be attributed to a specific alpha 1-adrenergic receptor
subtype that is blocked by WB 4101. These results have important
implications with respect to the induction of arrhythmias in the setting of
ischemia and the means for their prevention or treatment.
ARTICLES
Abnormal automatic rhythms in ischemic Purkinje fibers are modulated by a specific alpha 1-adrenergic receptor subtype
Institute of Experimental Cardiology, Cardiology Research Center, USSR, Moscow.
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