COLOCALIZATION OF NITRIC-OXIDE SYNTHASE AND VASOACTIVE-INTESTINAL-PEPTIDE IMMUNOREACTIVITY IN NEURONS OF THE MAJOR PELVIC GANGLION PROJECTING TO THE RAT RECTUM AND PENIS
T. Domoto et T. Tsumori, COLOCALIZATION OF NITRIC-OXIDE SYNTHASE AND VASOACTIVE-INTESTINAL-PEPTIDE IMMUNOREACTIVITY IN NEURONS OF THE MAJOR PELVIC GANGLION PROJECTING TO THE RAT RECTUM AND PENIS, Cell and tissue research, 278(2), 1994, pp. 273-278
Nitric oxide synthase (NOS)- and vasoactive intestinal peptide (VIP)-i
mmunoreactive neurons projecting to the upper rectum or penis were exa
mined using retrograde tracing combined with immunohistochemistry in t
he major pelvic ganglion of male rats. Five days after injection of Fl
uoro-Gold (FG) into the upper rectum or penis, the major pelvic gangli
on was treated with colchicine. FG injected into the upper rectum labe
lled many ganglion neurons in the major pelvic ganglion. Immunohistoch
emistry showed that 37% of FG-labelled neurons were immunoreactive for
NOS and 33% for VIP. After injection of FG into the penis, 41% of FG-
labelled neurons were immunoreactive for NOS and 25% for VIP. Serial c
ryostat sections stained for NOS and VIP, respectively, showed the co-
localization of NOS and VIP in the ganglion cells projecting to the re
ctum and penis. In the major pelvic ganglion of the colchicine-treated
animals, about 17% of the ganglion cells were immunoreactive for NOS
and 32% were immunoreactive for VIP. These neurons were small in diame
ter (less than 30 mu m) A histogram showing cell sizes in cross-sectio
nal areas of NOS-immunoreactive neurons coincided with that of VIP-imm
unoreactive neurons. Most of the NOS- and VIP-immunoreactive neurons w
ere less than 600 mu m(2) These results indicate that small neurons co
ntaining both NOS and VIP in the major pelvic ganglion project to the
rectum and penis. In the penile erectile tissues and enteric ganglia,
NO and VIP may be released from the same axons and may act concomitant
ly on the target tissue.