HYPOXIA AND ELECTRICAL-STIMULATION OF THE CAROTID-SINUS NERVE INDUCE FOS-LIKE IMMUNOREACTIVITY WITHIN CATECHOLAMINERGIC AND SEROTONINERGIC NEURONS OF THE RAT BRAIN-STEM
Jt. Erickson et De. Millhorn, HYPOXIA AND ELECTRICAL-STIMULATION OF THE CAROTID-SINUS NERVE INDUCE FOS-LIKE IMMUNOREACTIVITY WITHIN CATECHOLAMINERGIC AND SEROTONINERGIC NEURONS OF THE RAT BRAIN-STEM, Journal of comparative neurology, 348(2), 1994, pp. 161-182
A complete understanding of the neural mechanisms responsible for the
chemoreceptor and baroreceptor reflexes requires precise knowledge of
the locations and chemical phenotypes of higher-order neurons within t
hese reflex pathways. In the present study, the protein product (Fos)
of the c-fos protooncogene was used as a metabolic marker to trace cen
tral neural pathways following activation of carotid sinus nerve affer
ent fibers. In addition, immunohistochemical double-labeling technique
s were used to define the chemical phenotypes of activated neurons. Bo
th electrical stimulation of the carotid sinus nerve and physiological
stimulation of the carotid bodies by hypoxia induced Fos-like immunor
eactivity in catecholaminergic neurons containing tyrosine hydroxylase
or phenylethanolamine-N-methyltransferase in the ventrolateral medull
a oblongata and, to a lesser degree, in the dorsal vagal complex. Tyro
sine hydroxylase/Fos colocalization was also observed in the locus coe
ruleus and the Ag noradrenergic cell group in pens. Many serotoninergi
c neurons in nucleus raphe pallidus, nucleus raphe magnus, and along t
he ventral medullary surface contained Foe-like immunoreactivity. In p
ens and midbrain, Fos-like immunoreactivity was observed in the latera
l parabrachial and Kolliker-Fuse nuclei, the inferior colliculus, the
cuneiform nucleus, and in the vicinity of the Edinger-Westphal nucleus
, but no catecholaminergic or serotoninergic colocalization was observ
ed in these regions, Although Fos-labeled cells were observed within a
nd lateral to the dorsal raphe nucleus, few were catecholaminergic or
serotoninergic. This study further defines a potential central neuroan
atomical substrate for the chemoreceptor and/or baroreceptor reflexes.
(C) 1994 Wiley-Liss, Inc.