Ja. Madden et al., RESPONSES TO PRESSURE AND VASOACTIVE AGENTS BY ISOLATED PULMONARY-ARTERIES FROM MONOCROTALINE-TREATED RATS, Journal of applied physiology, 76(4), 1994, pp. 1589-1593
Intralobar and side branch pulmonary arteries removed from rats 7, 14,
and 21 days after injection with monocrotaline (MCT) were cannulated
and pressurized, and their responses to potassium chloride, norepineph
rine, acetylcholine, and angiotensin II were measured. Static pressure
-diameter curves were also performed, and arterial distensibility was
calculated. Arteries from all three MCT-treated groups showed reduced
responses to potassium chloride and angiotensin II compared with contr
ol arteries (P < 0.05). The norepinephrine response was significantly
reduced in arteries from the 14- and 21-day groups (P < 0.05). Dilatio
ns in response to acetylcholine were similar in arteries from the cont
rol and 7-day groups but were reduced compared with those in control v
essels from the 14- and 21-day groups (P < 0.05). Compared with contro
l values, the slopes of the pressure-diameter curves and the arterial
distensibility decreased significantly with time after MCT treatment (
P < 0.05). Values for arterial distensibilities obtained in the isolat
ed pulmonary arteries support the theory that structural changes that
occur as a result of MCT administration contribute to vessel stiffness
. The acetylcholine-induced dilation of vessels from MCT-treated rats
indicates that endothelium-derived factors are still produced, but dim
inished vasodilation coupled with decreased distensibilities after MCT
suggest that abnormal vascular remodeling rather than a change in ago
nist sensitivity may be responsible for the reduced responsiveness see
n in these arteries.