The coeliac ganglion of guinea pigs displays a unique topographical arrange
ment of neurochemically and functionally distinct populations of sympatheti
c neurons. The authors used multiple-labeling immunohistochemistry to inves
tigate the neurochemical differentiation of these neurons during embryonic
and fetal development. Sympathoadrenal precursors, located on either side o
f the abdominal aorta, were intensely immunoreactive for tyrosine hydroxyla
se (TH-IR), neurofilament, and the human natural killer 1 antibody at midem
bryonic stages (Carnegie stages 16-19). During late embryonic stages (stage
s 20-23), a single bilobed ganglion had formed. At this time, neuropeptide
Y immunoreactivity (NPY-IR) was widely expressed in sympathetic neurons (wi
th moderate TH-IR) and chromaffin cells (with intense TH-IR). The onset of
somatostatin (Som-IR) expression followed that of NPY-IR and was restricted
to sympathetic neurons. However, at late embryonic stages, most TH-IR neur
ons with Som-IR also expressed NPY-IR (a combination of peptides not found
in the mature coeliac ganglion). Between late embryonic stages and the end
of the early fetal period, there was a significant increase in the proporti
on of neurons in lateral regions that had both NPY-IR and TH-IR. At the sam
e time, there was an increase in the proportion of neurons in medial region
s that had both Som-IR and TH-LR. Neurons expressing both Som-IR and TH-IR
were rarely observed in lateral regions of the coeliac ganglion. Thus, a cl
ear topography within the coeliac ganglion is established during late embry
onic and early fetal stages of development and reflects that found in the m
ature animal by the end of the early fetal period. J. Comp. Neurol. 429:419
-435, 2001. (C) 2001 Wiley-Liss, Inc.