NITRIC-OXIDE SYNTHASE, CHOLINE-ACETYLTRANSFERASE, CATECHOLAMINE ENZYMES AND NEUROPEPTIDES AND THEIR COLOCALIZATION IN THE ANTERIOR PELVIC GANGLION, THE INFERIOR MESENTERIC GANGLION AND THE HYPOGASTRIC NERVE OFTHE MALE GUINEA-PIG
Lg. Elfvin et al., NITRIC-OXIDE SYNTHASE, CHOLINE-ACETYLTRANSFERASE, CATECHOLAMINE ENZYMES AND NEUROPEPTIDES AND THEIR COLOCALIZATION IN THE ANTERIOR PELVIC GANGLION, THE INFERIOR MESENTERIC GANGLION AND THE HYPOGASTRIC NERVE OFTHE MALE GUINEA-PIG, Journal of chemical neuroanatomy, 14(1), 1997, pp. 33-49
By the indirect immunofluorescence method, the distribution of nitric
oxide synthase (NOS)-like immunoreactivity (LI) and its possible coloc
alization with neuropeptide immunoreactivities, with two enzymes for t
he catecholamine synthesis pathway, tyrosine hydroxylase (TH) and dopa
mine beta-hydroxylase (DBH), as well as the enzyme for the acetylcholi
ne synthesis pathway, choline acetyltransferase (ChAT) were studied in
the anterior pelvic ganglion (APG), the inferior mesenteric ganglion
(IMG) and the hypogastric nerve in the male guinea pig. The analyses w
ere performed on tissues from intact animals, as well as after compres
sion/ligation or cut of the hypogastric nerve. In some cases the colon
ic nerves were also cut. Analysis of the APG showed two main neuronal
cell populations, one group containing NOS localized in the caudal par
t of the APG and one TK-positive group lacking NOS in its cranial part
. The majority of the NOS-positive neurons contained ChAT-LI. Some NOS
-positive cells did not contain detectable ChAT, but all ChAT-positive
cells contained NOS. NOS neurons often contained peptides, including
vasoactive intestinal peptide (VIP), neuropeptide tyrosine (NPY), soma
tostatin (SOM) and/or calcitonin gene-related peptide (CGRP). Some NOS
cells expressed DBH, but never TH. The second cell group, characteriz
ed by absence of NOS, contained TH, mostly DBH and NPY and occasionall
y SOM and CGRP. Some TH-positive neurons lacked DBH. In the IMG, the N
OS-LI was principally in nerve fibers, which were of two types, one co
nsisting of strongly immunoreactive, coarse, varicose fibers with a pa
tchy distribution, the other one forming fine, varicose, weakly immuno
reactive fibers with a more general distribution. In the coarse networ
ks, NOS-LI coexisted with VIP-and DYN-LI and the fibers surrounded mai
nly the SOM-containing noradrenergic principal ganglion cells. A netwo
rk of ChAT-positive, often NOS-containing nerve fibers, surrounded the
principal neurons. Occasional neuronal cell bodies in the IMG contain
ed both NOS-and ChAT-LI. Accumulation of NOS was observed, both caudal
and cranial, to a crush of the hypogastric nerve. VIP accumulated mai
nly on the caudal side and often coexisted with NOS. NPY accumulated o
n both sides of the crush, but mainly on the cranial side, and ENK was
exclusively on the cranial side. Neither peptide coexisted with NOS.
Both substance P (SP) and CGRP showed the strongest accumulation on th
e cranial side, possibly partly colocalized with NOS. It is concluded
that the APG in the male guinea-pig consists of two major complementar
y neuron populations, the cholinergic neurons always containing NOS an
d the noradrenergic neurons containing TH and DBH. Some NOS neurons la
cked ChAT and could represent truly non-adrenergic, non-cholinergic ne
urons. In addition, there may be a small dopaminergic neuron populatio
n, that is containing TH but lacking DBH. The cholinergic NOS neurons
contain varying combinations of peptides. The noradrenergic population
often contained NPY and occasionally SOM and CGRP. It is suggested th
at NO may interact with a number of other messenger molecules to play
a role both within the APG and IMG and also in the projection areas of
the APG. (C) 1997 Elsevier Science B.V.