Sa. Aicher et al., N-methyl-D-aspartate receptors are present in vagal afferents and their dendritic targets in the nucleus tractus solitarius, NEUROSCIENC, 91(1), 1999, pp. 119-132
N-Methyl-D-aspartate receptors are present in the nodose ganglion, which co
ntains the cell bodies of vagal afferents, and in the nucleus tractus solit
arius, where these afferent fibers terminate. This suggests that N-methyl-D
-aspartate receptors are located presynaptically on visceral vagal afferent
s and/or their target neurons in the nucleus tractus solitarius. To lest th
is hypothesis, we combined anterograde transport of biotinylated dextran am
ine, following injections into the left nodose ganglion, with electron micr
oscopic immunogold labeling of antipeptide antiserum against the R1 subunit
of the N-methyl-D-aspartate receptor in the nucleus tractus solitarius of
rat brain. Within the medial nucleus tractus solitarius, the N-methyl-D-asp
artate receptor R1 immunoreactivity was seen in dendrites (39% of 639 profi
les), axons and axon terminals (41%), and a few neuronal perikarya and glia
. Many vagal afferent axons and terminals (40% of 468 profiles) contained N
-methyl-D-aspartate receptor R1 immunogold labeling. In addition, 42% of th
e dendrites contacted by vagal afferent terminals (n = 206) contained N-met
hyl-D-aspartate receptor R1 immunoreactivity. In axons and dendrites, the g
old particles were occasionally seen within asymmetric postsynaptic junctio
ns or at non synaptic sites on the plasma membrane. More commonly, however,
N-methyl-D-aspartate receptor R1 labeling was seen on membranes of vesicul
ar cytoplasmic organelles, suggesting that there is abundant N-methyl-D-asp
artate receptor protein available for activity-dependent mobilization to th
e plasmalemma.
Since many vagal afferents are glutamatergic, our results implicate N-methy
l-D-aspartate receptors in autoregulation of the presynaptic release and po
stsynaptic responses to glutamate at the level of the first central synapse
in the nucleus tractus solitarius. (C) 1999 IBRO. Published by Elsevier Sc
ience Ltd.