Mr. Melis et al., NITRIC-OXIDE PRODUCTION IS INCREASED IN THE PARAVENTRICULAR NUCLEUS OF THE HYPOTHALAMUS OF MALE RATS DURING NONCONTACT PENILE ERECTIONS ANDCOPULATION, European journal of neuroscience, 10(6), 1998, pp. 1968-1974
Male rats put in the presence of a receptive female rat that they can
see, hear and smell, but cannot touch, show penile erection episodes.
These non-contact erections occur concomitantly with an increase in ni
tric oxide production in the paraventricular nucleus of the hypothalam
us, as detected by the increase in the NO2- and NO3- concentration in
the paraventricular dialysate obtained from these males by in vivo mic
rodialysis. NO2- concentration increased from 0.81 +/- 0.12 to 2.51 +/
- 0.43 mu M and that of NO3- from 4.50 +/- 0.73 to 8.31 +/- 2.3 mu M.
The NO2- increase was prevented by the nitric oxide synthase inhibitor
NG-nitro-L-arginine methylester (20 mu g) given unilaterally in the p
araventricular nucleus, which also prevented non-contact erections. In
contrast, the nitric oxide scavenger haemoglobin (20 mu g) prevented
the NO2- increase, but not non-contact erections; while the guanylate
cyclase inhibitor methylene blue (20 mu g) was ineffective on either r
esponse. NO2- and NO3- concentration was also increased in the paraven
tricular dialysate of male rats during in copula penile erections, tha
t is, when sexual activity was allowed with the receptive females. As
found with non-contact erections, N-G-nitro-L-arginine methylester pre
vented NO2- increase and impaired copulatory behaviour; haemoglobin pr
evented NO2- increase only; and methylene blue was ineffective on eith
er response. The present results confirm that nitric oxide is a physio
logical mediator of penile erection at the level of the paraventricula
r nucleus of the hypothalamus.