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Departments of 1 Surgery and 2 Pharmacology and Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
Second-order
middle cerebral arteries (135.0 ± 4.6 µm ID) from male, female,
ovariectomized female (no endogenous estrogen), and estrogen-treated
ovariectomized female Sprague-Dawley rats were harvested and mounted in
a pressure myograph. Myogenic response was recorded over a pressure
range of 10-100 mmHg and was repeated in the presence of
N
-nitro-L-arginine
methyl ester (L-NAME; 2 × 10
4 M), an inhibitor of
nitric oxide (NO) synthase, and after endothelium removal, to examine
the contribution of NO to net myogenic tone. With intact endothelium,
there were no differences in myogenic tone between the groups, but in
the presence of L-NAME and after endothelium removal, estrogen-exposed vessels developed significantly greater tone at high transmural pressure. There were no differences in
sensitivity to sodium nitroprusside, an NO donor, or A-23187, a calcium
ionophore. These results suggest an increase in basal release of NO in
cerebral arteries exposed to estrogen, without change in NO sensitivity
or maximally stimulated NO release.
cerebral circulation; autoregulation; endothelium; wall tension; vasoprotection
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