Intravenous phenylephrine (PE) activates neurons in the nucleus of the soli
tary tract (NTS) whose distribution conforms to those of central projection
s of the carotid sinus and aortic depressor nerves. This was exploited to p
ermit fine structural characterization of cells presumed to compose the fir
st station in the processing of arterial baroreceptor input, and their resp
onses to stimulation. Rats were perfused at varying intervals after PE inje
ction, and sections through the baroreceptor afferent zone of the NTS prepa
red for preembedding immunolocalization of Fos-immunoreactivity. Labeled ne
urons composed a continuous strip extending from the dorsal part of the com
missural NTS (NTScom) to the dorsal subnucleus at the level of the area pos
trema (NTSap). PE-sensitive neurons in these regions were medium-sized, rou
nd to ovoid in shape, with scant cytoplasm and an unremarkable complement o
f organelles. Distinctive features included extensively invaginated nuclei
and well-developed Golgi apparati; Fos-ir cells in the NTSap were distingui
shed from those in NTScom by virtue of better-developed rough endoplasmic r
eticulum and Golgi, and less convoluted nuclei. Proximal synaptic input to
PE-sensitive neurons was sparse and was provided by terminals containing pr
edominantly small, clear synaptic vesicles that formed mainly symmetric jun
ctions with somata and primary dendrites. Prolonged stimulation was accompa
nied by accentuation of nuclear invaginations, marked accumulation of heter
ochromatin at their apices, and evidence of enhanced Golgi activity (vesicu
lar budding). These may represent adaptations to facilitate changes in gene
expression, to maintain neurotransmitter availability, or both, in the fac
e of a persistent hypertensive challenge. J. Comp. Neurol. 422:338-351, 200
0. (C) 2000 Wiley-Liss, Inc.