The rostral end of the ventral respiratory group (VRG) contains neurons tha
t are intensely neurokinin-l receptor (NK1R) immunoreactive (ir). It has be
en theorized that some of these cells might be critical to respiratory rhyt
hmogenesis (Cray et al. [1999] Science 286:1566-1568). In the present study
we determined what major transmitter these NK1R-ir cells make and whether
they are bulbospinal or propriomedullary. NK1R-ir neurons were found in the
VRG between Bregma levels -11.7 and -13.6 mm. The highest concentration wa
s found between Bregma -12.3 and -13.0 mm. This region overlaps with the pr
e-Botzinger complex (pre-BotC) as it was found to contain many pre-inspirat
ory neurons, few E2-expiratory neurons, and no I-incremental neurons. VRG N
K1R-ir neurons contain neither tyrosine hydroxylase (TH) nor choline acetyl
transferase (ChAT) immunoreactivity, although dual-labeled neurons were fo
und elsewhere within the rostral medulla. GAD67 mRNA was commonly detected
in the ventrolateral medulla (VLM) but rarely in the NK1R-ir neurons of the
pre-BotC region (6 % of somatic profiles). GlyT2 mRNA was commonly found i
n the pre-BotC region but rarely within NK1R-ir neurons (1.3 %). Up to 40%
of VRG NK1R-ir neurons were retrogradely labeled by Fluoro-Gold (FG) inject
ed in the contralateral pre-BotC region. Some NK1R-ir VRG neurons located c
audal to Bregma -12.6 mm were retrogradely labeled by FG injected in the sp
inal cord (C4-C5, T2-T4). In sum, NK1R immunoreactivity is present in many
types of ventral medullary neurons. Within the VRG proper, NK1R-ir neurons
are concentrated in an area that overlaps with the pre-BotC. Within this li
mited region of the VRG, NK1R-ir neurons are neither cholinergic nor catech
olaminergic, and very few are gamma -aminobutyric acid (GABA)ergic or glyci
nergic. The data suggest that most NK1R-ir neurons of the pre-BotC region a
re excitatory. Furthermore, the more rostral NR1R-ir cells are propriomedul
lary, whereas some of the caudal ones project to the spinal cord. (C) 2001
Wiley-Liss, Inc.