(Hypertension. 1997;30:1210-1215.)
© 1997 American Heart Association, Inc.
Articles |
From the Department of Physiology, New York Medical College, Valhalla, NY.
Abstract We hypothesized that endothelin in addition to
prostaglandin (PG)H2 may also contribute to the
enhanced myogenic tone of skeletal muscle arterioles of spontaneously
hypertensive (SH) rats. Changes in the diameter of isolated, cannulated
arterioles (
60 µm) from cremaster muscles of 30-week-old
normotensive Wistar Kyoto (WKY) and SH rats were measured as a function
of perfusion pressure (20 to 140 mm Hg). Pressure-induced
constrictions were significantly enhanced between 60 to 140 mm Hg
in arterioles of SH rats compared with those of WKY rats; at 80 and
140 mm Hg the normalized diameter of arterioles (expressed as a
percentage of corresponding passive diameter) of SH rats was 11.0% and
15.4% less (P<.05) than that of WKY rats. After inhibition
of thromboxane A2PGH2 receptors
by SQ 29,548 (10-6 mol/L), the still enhanced
myogenic response of SH arterioles was eliminated by the removal of
endothelium or the administration of BQ-123
(10-7 mol/L), an endothelin A (ET-A) receptor
blocker, which also inhibited constrictions to exogenous ET-1
(10-11 to 5x10-10
mol/L). ET-1 elicited comparable responses in arterioles of SH and WKY
rats. Thus, in SH rats the enhanced arteriolar constriction to
increases in intravascular pressure seems to be due to the
production of endothelium-derived constrictor
factors PGH2 and endothelin.
Key Words: hypertension, genetic myogenic tone arterioles intraluminal pressure endothelium
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