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Vol. 280, Issue 2, 721-729, 1997
Department of Pharmacology, The purpose of our study was to investigate the inotropic response to
the endogenous agonist norepinephrine mediated through alpha-1 adrenoceptors and to compare this response to
that mediated through beta-adrenoceptors in failing human
ventricular myocardium. We studied ex vivo the inotropic
effect of norepinephrine in isometrically contracting trabecular
myocardium from both ventricles of explanted hearts. By studying
influence of appropriate adrenoceptor blockers, qualitative
characteristics of the inotropic response and sensitivity of the
inotropic response to cholinergic stimulation, it was revealed that
norepinephrine evoked both alpha-1 and
beta adrenoceptor-mediated inotropic effects in failing
human ventricle myocardium. Quantitatively the inotropic responses to
norepinephrine varied markedly between preparations, but the mean
responses elicited through the respective adrenoceptor systems were of
comparable magnitude. Concomitant stimulation of alpha-1
and beta adrenoceptors by norepinephrine alone revealed
a contribution of an alpha-1 adrenoceptor-mediated component to the final and unopposed inotropic response. Differential sensitivity of the two adrenoceptor systems to norepinephrine depending
on etiology of heart failure and possibly also thyroid status was
observed. It is concluded that norepinephrine evokes an
alpha-1 adrenoceptor-mediated inotropic effect
comparable to that evoked through the beta adrenoceptors
in failing human ventricular myocardium, and that this
alpha-1 adrenoceptor-mediated inotropic effect may be of
functional importance.
Copyright © by The American Society for Pharmacology and Experimental Therapeutics
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