Gg. Del Cano et al., Ionotropic glutamate receptor subunits are differentially regulated in themotoneuronal pools of the rat hypoglossal nucleus in response to axotomy, J NEUROCYT, 29(7), 2000, pp. 509-523
Unilateral hypoglossal nerve axotomy was used as a model to analyse immunoh
istochemically the expression of the GluR1, GluR2, GluR3, and GluR4 glutama
te receptor subunits of the alpha -amino-3-hydroxy-5-methyl-4-isoxazoleprop
ionate (AMPA) subtype and the NR1 subunit of the N-methyl-D-aspartate (NMDA
) subtype in the different morphofunctional hypoglossal pools from 1 to 45
days postaxotomy. Following hypoglossal nerve axotomy, the percentage of mo
toneurons that were GluR1-immunopositive and the labeling intensity for thi
s subunit was increased in some hypoglossal pools. Immunolabeling for the G
luR2 subunit was undetectable. These results contrast with the unchanged pa
ttern for these two subunits after sciatic nerve axotomy previously describ
ed. Image analysis showed a significant decrease in the intensity of immuno
histochemical labeling for the GluR2/3 and GluR4 subunits in motoneurons, a
lthough most motoneurons were still immunopositive for these 2 subunits aft
er axotomy. The intensity of immunolabeling for the NR1 subunit was slightl
y decreased postlesion, whereas the percentage of NR1-immunopositive motone
urons increased. Immunoreactivity returned to basal levels 45 days postlesi
on. These findings show that in axotomized hypoglossal motoneurons, i) AMPA
and NMDA receptor subunits are still expressed, ii) the composition of the
ionotropic glutamate receptor subunit pool is subjected to continuous chan
ges during the regeneration process, iii) AMPA receptors, if functional, wo
uld have physiological properties different to those in intact motoneurons,
and iv) the various AMPA receptor subunits are differentially regulated. T
he present results also suggest a faster recovery of basal levels of immuno
reactivity for caudally localised groups of motoneurons which could reflect
a caudo-rostral sequential functional revovery in the hypoglossal nucleus.