Y. Nagase et al., SEROTONERGIC AXONAL CONTACTS ON IDENTIFIED CAT TRIGEMINAL MOTONEURONSAND THEIR CORRELATION WITH MEDULLARY RAPHE NUCLEUS STIMULATION, Journal of comparative neurology, 384(3), 1997, pp. 443-455
The innervation of the trigeminal motor nucleus by serotonergic fibers
with cell bodies in the raphe nuclei pallidus and obscurus suggests t
hat activation of this pathway may alter the excitability of trigemina
l motoneurons. Thus, we recorded intracellular responses from cat jaw-
closing (JC) and jaw-opening (JO) alpha-motoneurons evoked by raphe st
imulation and used a combination of intracellular staining of horserad
ish peroxidase (HRP) and immunohistochemistry at the light and electro
n microscopic levels to examine the distribution of contacts made by s
erotonin (5-HT)-immunoreactive boutons on the two motoneurons types. E
lectrical stimulation applied to the nucleus raphe pallidus-obscurus c
omplex induced a monosynaptic excitatory postsynaptic potential (EPSP)
in JC (masseter) alpha-motoneurons and an EPSP with an action potenti
al in JO (mylohyoid) alpha-motoneurons. The EPSP rise-times (time to p
eak) and half widths were significantly longer in the JC than in the J
O motoneurons. The EPSPs were suppressed by systemic administration of
methysergide (2 mg/kg). Six JC and seven JO alpha-motoneurons were we
ll stained with HRP. Contacts were seen between 5-HT-immunoreactive bo
utons and the motoneurons. The JC motoneurons received a significantly
larger number of the contacts than did the JO motoneurons. The contac
ts were distributed widely in the proximal three-fourths of the dendri
tic tree of JC motoneurons but were distributed on more proximal dendr
ites in the JO motoneurons. At the electron microscopic level, synapti
c contacts made by 5-HT-immunoreactive boutons on motoneurons were ide
ntified. The present study demonstrated that JC motoneurons receive st
ronger 5-HT innervation, and this correlates with the fact that raphe
stimulation caused larger EPSPs among these neurons than among JO moto
neurons. (C) 1997 Wiley-Liss, Inc.