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Division of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21224
In isolated porcine pulmonary arterioles with
endothelium, intraluminal diameter measured at a transmural pressure of
20 mmHg decreased spontaneously from 233 ± 11 to 171 ± 12 µm in 135 min. This intrinsic constriction was not
prevented by indomethacin, tetraethylammonium, or superoxide dismutase.
Indomethacin plus NG-nitro-L-arginine
methyl ester caused initial constriction and BQ-123 or BQ-123 plus
BQ-788 caused initial dilation, but these treatments did not prevent
subsequent progressive constriction. In pulmonary arterioles with
endothelium exposed to calcium-free conditions and pulmonary arterioles
without endothelium, the intraluminal diameter measured at a transmural
pressure of 20 mmHg was constant at 239 ± 16 and 174 ± 7 µm,
respectively. Thus the spontaneous development of tone in isolated
pulmonary arterioles required extracellular calcium and resulted from
1) time-independent smooth muscle
contraction caused by mechanisms intrinsic to smooth muscle and
2) time-dependent contraction caused
by decreasing activity of endothelium-derived relaxing factors other
than nitric oxide, vasodilator prostaglandins, and hyperpolarizing
factors acting on calcium-dependent potassium channels or increasing
activity of endothelium-derived contracting factors other than
endothelin-1, vasoconstrictor prostaglandins, and superoxide anions.
Further investigation is indicated to identify these unknown mechanisms and determine their role in pulmonary vasoreactivity.
endothelium-derived relaxing factor; endothelium-derived contracting factor; nitric oxide; prostaglandins; endothelin-1; superoxide anions; extracellular calcium concentration; pig
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