OBJECTIVE: To examine the hypothesis that kinetics of vasorelaxation a
re altered during pregnancy. METHODS: Rings of aorta from rats at diff
erent stages of pregnancy (early, late, and term) and from nonpregnant
female rats were precontracted with high-K+ and then allowed to relax
in normal-K+ physiologic saline solution. The time to reach 50% and 8
0% relaxation were determined in the absence or presence of a cyclooxy
genase inhibitor (indomethacin) and a nitric oxide synthase inhibitor
(N-omega-nitro-L-arginine methyl ester) or after removal of the endoth
elium. RESULTS: The aortic relaxation was progressively faster in late
r stages of gestation. N-omega-nitro-L-arginine methyl ester and indom
ethacin had no significant effect whereas removal of the endothelium c
aused a slowing of relaxation in all the groups. Even in the presence
of N-omega-nitro-L-arginine methyl ester and indomethacin or after de-
endothelization, the relaxation remained faster at term as compared wi
th the other groups. CONCLUSION: Aortic relaxation is faster in the pr
esence of endothelium. The effect of endothelium on relaxation is inde
pendent of nitric oxide synthase or cyclooxygenase systems. Progressio
n of gestation is associated with acceleration of aortic relaxation, w
hich cannot be totally ascribed to an endothelial factor and may invol
ve a change intrinsic to the vascular smooth muscle. Faster relaxation
kinetics of the vasculature during pregnancy may be a mechanism to de
crease peripheral vascular resistance. (C) 1998 by the Society of Gyne
cologic Investigation.