Stroke, Vol 19, 1145-1150, Copyright © 1988 by American Heart Association
CT Stier Jr, IF Benter and S Levine
Thromboxane A2 is a prostanoid having potent platelet aggregatory and
vasoconstrictor properties. To determine a possible role for thromboxane A2
in the development of severe hypertension and stroke, we chronically
administered the selective thromboxane A2 synthase inhibitor UK-38,485
(Dazmegrel) to stroke-prone spontaneously hypertensive rats (SHRSP). Serum
thromboxane B2 (the stable hydrolysis product of thromboxane A2) generation
was significantly greater in incubates of whole blood from SHRSP than in
those from normotensive control Wistar-Kyoto rats and was inhibited greater
than 89% by UK- 38,485 administered in vivo. In 10 male SHRSP fed a
Japanese-style rat chow and given 1% NaCl in drinking water to accelerate
the occurrence of stroke, treatment with 100 mg/kg/day UK-38,485 by gavage
starting at 8.6 weeks of age diminished systolic blood pressure elevation
at 10 (205 +/- 2 vs. 220 +/- 4 mm Hg, p less than 0.01) and 11 weeks of age
(210 +/- 4 vs. 239 +/- 7 mm Hg, p less than 0.01) compared with 10
untreated SHRSP. The ultimate establishment of severe hypertension was not
prevented by UK-38,485. Stroke-related mortality was 70% in both UK-
38,485-treated and control SHRSP at 14 weeks of age. Histologic examination
revealed cerebrovascular lesions consistent with the occurrence of stroke
in both control and UK-38,485-treated SHRSP. Our results support a possible
role for thromboxane A2 in the elevation of blood pressure in SHRSP but do
not support a possible role for the prevention of stroke by thromboxane A2
synthase inhibition in these rats.
ARTICLES
Thromboxane A2 in severe hypertension and stroke in stroke-prone spontaneously hypertensive rats
Department of Pharmacology, New York Medical College, Valhalla 10595.
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