Am. Schreinhofer et Pg. Guyenet, IDENTIFICATION OF C1 PRESYMPATHETIC NEURONS IN RAT ROSTRAL VENTROLATERAL MEDULLA BY JUXTACELLULAR LABELING IN-VIVO, Journal of comparative neurology, 387(4), 1997, pp. 524-536
The rostral ventrolateral medulla (RVLM) contains barosensitive, bulbo
spinal neurons that provide the main supraspinal excitatory input to s
ympathetic vasomotor preganglionic neurons. However, the phenotype of
the critical RVLM cells has not been conclusively determined. The goal
of the current study was to identify the proportion of electrophysiol
ogically defined, putative, presympathetic RVLM neurons that are C1 ce
lls. We used a juxtacellular labeling technique to individually fill s
pontaneously active, barosensitive, bulbospinal RVLM neurons with biot
inamide following electrophysiological characterization in chloralose-
anesthetized rats. To determine whether these neurons could be classif
ied as C1 cells, the biotinamide-labeled cells were processed for dete
ction of tyrosine hydroxylase. The majority of barosensitive bulbospin
al RVLM neurons were tyrosine hydroxylase immunoreactive (TH-ir: 28 of
39). All of the barosensitive bulbospinal RVLM neurons with axonal co
nduction velocities in the C fiber range (<1 m/second) were TH-ir (n =
16), whereas faster conducting cells (1 to 7 m/second) were either li
ghtly TH-ir (n = 12) or not detectably TH-ir (n = 11). Adjacent respir
atory-related RVLM units labeled with biotinamide were not detectably
TH-ir (n = 10). To verify that TH-ir cells were indeed adrenergic, a s
ubset of barosensitive bulbospinal cells labeled with biotinamide were
examined for phenylethanolamine N-methyltransferase immunoreactivity
(PNMT-ir). Three slowly conducting cells had detectable PNMT-ir, and t
wo fast-conducting cells had no detectable PNMT-ir. These results indi
cate that the majority of bulbospinal RVLM neurons with putative sympa
thoexcitatory function are C1 cells. J. Comp. Neurol. 387:524-536, 199
7. (C) 1997 Wiley-Liss, Inc.