Circulation, Vol 72, 397-405, Copyright © 1985 by American Heart Association
P Apprill, JM Schmitz, WB Campbell, G Tilton, J Ashton, S Raheja, LM Buja and JT Willerson
The phospholipid platelet-activating factor (PAF) stimulates platelet
aggregation and coronary vasoconstriction. In this study we determined
whether PAF alters coronary flow patterns in vivo in a canine preparation
with concentric coronary artery stenosis. This preparation is characterized
by cyclic flow variations in coronary blood flow associated with transient
platelet aggregation at the site of the coronary constriction. Thirty-nine
male mongrel dogs were used in three protocols. In protocol 1, PAF (10(-9)
or 10(-8) mol/min) was infused into the coronary artery proximal to the
stenosis to determine (1) whether PAF induces cyclic flow variations and
(2) whether PAF has an effect on systemic hemodynamics. Cyclic flow
variations were induced in three of six dogs; in these animals, mean
arterial pressure decreased by 5.5% and 42.1% 10 min after infusion of the
lower and higher dose of PAF. In protocol 2, cyclic flow variations were
abolished with either the thromboxane synthetase inhibitor UK38485 (mean
dose 2.2 mg/kg iv), the serotonin antagonist ketanserin (0.5 mg/kg iv), or
the alpha 2- adrenergic antagonist yohimbine (2 mg/kg iv). Subsequent
administration of PAF restored the frequency of cyclic flow variations to
the preantagonist levels. Thromboxane (Tx) B2 and 6-keto-PGF1 alpha, the
stable metabolites of TxA2 and prostacyclin, respectively, were measured in
blood obtained distal to the coronary stenosis. TxB2 levels increased
substantially during cyclic flow variations and were returned to control
values with the thromboxane synthetase inhibitor UK38485. Infusion of PAF
subsequently restored cyclic flow variations without altering coronary
arterial coronary arterial TxB2 levels.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Cyclic blood flow variations induced by platelet-activating factor in stenosed canine coronary arteries despite inhibition of thromboxane synthetase, serotonin receptors, and alpha-adrenergic receptors
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