Stroke, Vol 19, 476-479, Copyright © 1988 by American Heart Association
ZS Katusic, JT Shepherd and PM Vanhoutte
The effects of the calcium ionophore A23187, arachidonic acid, and
acetylcholine were studied in isolated canine basilar arteries. Rings with
and without endothelium were suspended for isometric tension recording in
physiological saline. In unstimulated rings, A23187, arachidonic acid, and
acetylcholine caused endothelium-dependent contractions. The contractions
of rings caused by uridine 5'- triphosphate were not affected by removal of
the endothelium. An inhibitor of cyclooxygenase, indomethacin (10(-5) M),
prevented excitatory responses to A23187, arachidonic acid, and
acetylcholine but did not alter contractions caused by KCl. An inhibitor of
thromboxane synthetase, dazoxiben (10(-4) M), significantly reduced
endothelium- dependent contractions to A23187 and arachidonic acid but did
not significantly affect contractions caused by acetylcholine. These
results demonstrate that A23187, arachidonic acid, and acetylcholine cause
excitatory endothelium-dependent responses in canine cerebral blood vessels
by increasing the release of product(s) of cyclooxygenase from endothelial
cells; in the case of A23187 and arachidonic acid, thromboxane A2
contributes to the endothelium-dependent contractions.
ARTICLES
Endothelium-dependent contractions to calcium ionophore A23187, arachidonic acid, and acetylcholine in canine basilar arteries
Department of Physiology and Biophysics, Mayo Clinic, Rochester, MN 55905.
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