Different expressions of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid and N-methyl-D-aspartate receptor subunit mRNAs between visceromotor and somatomotor neurons of the rat lumbosacral spinal cord
T. Shibata et al., Different expressions of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid and N-methyl-D-aspartate receptor subunit mRNAs between visceromotor and somatomotor neurons of the rat lumbosacral spinal cord, J COMP NEUR, 404(2), 1999, pp. 172-182
The glutamatergic transmission system plays a key role in afferent and effe
rent pathways involved in micturition. By in situ hybridization combined wi
th retrograde Fast Blue labeling, expression of alpha-amino-3-hydroxy-5-met
hyl-4-isoxazole propionic acid (AMPA) receptor (GluR-A to -D) and N-methyl-
D-aspartate (NMDA) receptor (NR1 and NR2A-D) subunit mRNAs were examined in
visceromotor and somatomotor neurons of the rat lumbosacral spinal cord. P
arasympathetic preganglionic neurons (PC;Ns) in the intermediolateral nucle
us highly expressed GluR-A and GluR-B subunit mRNAs, with very low levels f
or GluR-C and GluR-D subunits. As for the NMDA receptor, PGNs were associat
ed with abundant signals for NR1 subunit mRNA, but without any NR2 subunit
mRNAs. On the other hand, somatomotor neurons in the ventral horn (dorsolat
eral nucleus) express all four AMPA receptor subunit mRNAs, showing relativ
ely abundant expressions of GluR-C and GluR-D subunit mRNA compared with PG
Ns. In addition to high levels of NR1 subunit mRNA, dorsolateral nucleus ne
urons moderately expressed NR2A and NR2B subunit mRNAs. These results sugge
st that molecular organization of both AMPA and NMDA receptor channels are
distinct between PGNs and dorsolateral nucleus neurons. Considering that na
tive NMDA receptors are heteromeric channels composed of NR1 and NR2 subuni
ts, it seems Likely that dorsolateral nucleus neurons, not PGNs, are provid
ed with functional NMDA receptors, which could induce activity-dependent ch
anges in synaptic transmission in the efferent pathway for the lower urinar
y tract. (C) 1999 Wiley-Liss, Inc.