Isolated uterine vascular beds from virgin and pregnant rats were used to a
ssess vascular reactivity and the ability of nitric oxide (NO), prostanoids
and endothelium-derived hyperpolarizing factor (EDHF) to modulate these re
sponses. One uterine horn from female rats in each oestrous cycle day and g
estation day 17 was removed and perfused with physiological saline solution
. Tone was induced with cirazoline (1 mu mol/l), and concentration-response
curves to acetylcholine (ACh) generated. Responsiveness to ACh was tested
in the presence of N-nitro-L-arginine (L-NA), ibuprofen (IBU) and tetrabuty
lammonium (TBA), to inhibit NO synthase, cyclo-oxygenase and K+ channels re
spectively. Cirazoline-induced tone was smaller in the pregnant compared wi
th the proestrous group. Sensitivity to ACh was cycle day and pregnancy dep
endent with pregnant > dioestrous day-1 > dioestrous day-2 > proestrous and
oestrous. L-NA shifted the curve to the right in all groups except dioestr
ous day-1. IBU inhibited the ACh response in the pregnant group only. TBA v
irtually abolished the response in all groups. These results suggest that i
n the uterine vascular bed from pregnant rats, EDHF, along with NO and a di
lator prostanoid mediate ACh-induced dilatation, In contrast, in the dioest
rous day-1 group, only EDHF seems to be released by ACh in this vascular be
d. Lu the oestrous, dioestrous day-2 and proestrous groups, ACh releases bo
th EDHF and NO.