Sp. Martinez et al., Effect of nitric oxide synthase inhibitors on ovum transport and oviductalsmooth muscle activity in the rat oviduct, J REPR FERT, 118(1), 2000, pp. 111-117
The effect of the inhibition of nitric oxide synthase (NOS) on ovum transpo
rt and oviductal motility in rats was investigated. Three different NOS inh
ibitors were injected into the ovarian bursa at oestrus or day 3 of pregnan
cy. Oviducts and uteri were flushed 24 h later and the presence of ova was
recorded. In oestrous and pregnant rats, treatment resulted in accelerated
egg transport, as shown by a decrease in the number of ova present in the o
viducts. In cyclic rats, intrabursal injection of 1 mg kg(-1) of either N-m
onomethyl-L-arginine (L-NMMA) or N-omega nitro-L-arginine methyl ester (L-N
AME) elicited a 30% reduction in the number of ova present in the oviducts,
whereas in pregnant animals, the same dose of L-NMMA produced a reduction
of 40%. Simultaneous administration of the NO donor spermine NONOate (5 mg
kg(-1)) completely reversed the effect of L-NMMA. Tubal motility was assess
ed by microsphere displacement analysis within the oviduct. Surrogate ova w
ere transferred to the oviductal lumen at oestrus and 24 h later the effect
of intraoviductal injection of 1 mu g L-NMMA or vehicle was assessed. The
microspheres in the isthmus showed an oscillating motion, and periods in wh
ich movement was not detectable. However, L-NMMA treatment produced a 3.6-f
old increase in the maximum instant velocities and a significant reduction
in the resting periods of the microspheres compared with the control group
(P < 0.001). These results provide evidence that NO inhibition increases tu
bal motility that results in accelerated ovum transport, and indicate that
NO could act as a paracrine signal between different layers of the oviducta
l wall, providing a role for endogenous NO in regulation of tubal function.