Ae. Christie et al., ORGANIZATION OF THE STOMATOGASTRIC NEUROPIL OF THE CRAB, CANCER-BOREALIS, AS REVEALED BY MODULATOR IMMUNOCYTOCHEMISTRY, Cell and tissue research, 288(1), 1997, pp. 135-148
We used antibodies to a number of neuromodulatory substances, includin
g serotonin, FLRF Amide, red pigment-concentrating hormone, substance
P, proctolin and cholecystokinin, to investigate the distribution of m
olecules similar to these substances in the stomatogastric ganglion of
the crab, Cancer borealis. No immunoreactivity was seen in the region
of the cell bodies that surrounds the neuropil and little was found i
n the core of the neuropil (where the primary neurites of the intrinsi
c neurons occupy most of the space). Instead, modulator immunolabel wa
s densely packed in the more peripheral portion of the neuropil that s
urrounded the core. Within this peripheral neuropil, profiles appeared
quite uniformly distributed. Double-labeling showed that there were l
imited differences in distribution between the labels examined in our
study. The only immunolabeled structures that showed a distinct differ
ential distribution within the stomatogastric neuropil were a populati
on of greater than or equal to 10 mu m Varicosities that arose from a
pair of input fibers that we termed the large varicosity fibers. These
varicosities were immunolabelled by antisera for three different pept
ides. Taken collectively, these data shows that there is a stereotyped
distribution of modulator immunoreactivity within the crab stomatogas
tric neuropil. However, this segregation is more rudimentary than that
reported for the intrinsic stomatogastric neurons.