Hypertension, Vol 21, 289-293, Copyright © 1993 by American Heart Association
CM Boulanger and PM Vanhoutte
The present experiments were designed to investigate the effect of
interleukin-2 on the response to arachidonic acid in rings with and without
endothelium from Wistar-Kyoto (WKY) and spontaneously hypertensive rat
(SHR) aortas. In control rings, arachidonic acid induced contractions of
WKY aorta that were not different between preparations with and without
endothelium. Incubation with interleukin- 2 (10 units/mL) for 6 or 18 hours
augmented the response to arachidonic acid in rings with, but not in those
without, endothelium from WKY rat aortas. In the WKY aorta, both the
endothelium-dependent and endothelium-independent contractions to
arachidonic acid observed after incubation with interleukin-2 were
abolished by indomethacin and ridogrel (a thromboxane-endoperoxide receptor
antagonist and a thromboxane synthase inhibitor) but were not affected by
dazoxiben (a thromboxane synthase inhibitor). Interleukin-2 did not augment
the vascular reactivity of WKY aortic smooth muscle to activation of the
thromboxane-endoperoxide receptor with U46619. In aortas from SHRs,
arachidonic acid evoked endothelium-dependent contraction; interleukin- 2
did not modify the response to arachidonic acid in preparations with and
without endothelium. These data demonstrate that 1) endothelium- dependent
contractions to arachidonic acid are observed in SHR but not in WKY rat
aortas; 2) interleukin-2 induces endothelium-dependent contractions to
arachidonic acid in the WKY aorta that are mediated by an augmented release
of a metabolite of cyclooxygenase, different from thromboxane A2 but
activating thromboxane-endoperoxide receptors; and 3) interleukin-2 does
not affect the endothelium-dependent and endothelium-independent response
to arachidonic acid in the SHR aorta.
ARTICLES
Interleukin-2 causes endothelium-dependent contractions to arachidonic acid
Department of Medicine-Hypertension, Baylor College of Medicine, Houston, Tex. 77030.
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