Circulation, Vol 69, 889-894, Copyright © 1984 by American Heart Association
R De Caterina, C Carpeggiani and A L'Abbate
This study was designed to test the hypothesis of a possible role of
serotonin in the pathogenesis of myocardial ischemia in patients with pure
vasospastic angina, since serotonin is known to cause contraction in
isolated coronary arteries. This effect, as well as serotonin- induced
platelet aggregation, is reversed by ketanserin, a specific S2- receptor
blocker. Five male patients (49 to 68 years old) with more than six
episodes/day of myocardial ischemia at rest as characterized by ST segment
elevation on the electrocardiogram (ECG) were selected for the study after
a 2 day run-in period of continuous ECG Holter monitoring in the absence of
any therapy except that with sublingual nitrates. In a double-blind
crossover protocol they received consecutive infusions of 6 hr each of
ketanserin (2 mg/hr iv, preceded by a 10 mg bolus in three patients) and
placebo in the following sequence: ketanserin-placebo-ketanserin-placebo in
the first and placebo-ketanserin-placebo-ketanserin in the second 24 hr
period. The efficacy of the infused drug was tested by exposing
platelet-rich plasma, obtained from the study patients at a fixed morning
time before and during ketanserin infusions, to a series of serotonin
concentrations from 10(-5) to 10(-8)M in a conventional aggregometer. A
complete suppression of aggregation curves in the range of serotonin
concentrations tested resulted during administration of ketanserin. The
efficacy of the drug in preventing ischemic episodes was assessed by
computing the ischemic episodes (recorded by Holter monitoring) and
nitroglycerin consumption in each 6 hr ketanserin period and in the
corresponding placebo period. A total of 171 ischemic episodes were
recorded, 33 of which (19%) were symptomatic.(ABSTRACT TRUNCATED AT 250
WORDS)
ARTICLES
A double-blind, placebo-controlled study of ketanserin in patients with Prinzmetal's angina. Evidence against a role for serotonin in the genesis of coronary vasospasm
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