We have reported previously that axotomy induced a marked increase of vasop
ressin receptor binding in the adult rat facial nucleus, suggesting an incr
eased number of vasopressin receptors. These receptors were pharmacological
ly undistinguishable from peripheral V-1a vasopressin receptors. In the pre
sent study, we show, using in situ hybridization and reverse transcriptase-
polymerase chain reaction (RT-PCR), that axotomy regulates the expression o
f the vasopressin V-1a receptor mRNA in the facial nucleus. Results were ob
tained from adult male rats killed 1 week following crush of the right faci
al nerve. In situ hybridization was performed with a S-35-labelled riboprob
e. A specific hybridization signal was detected in both left and right faci
al nuclei, with a significantly higher intensity in the nucleus ipsilateral
to the lesion. V-1a receptor transcripts were found associated with large
facial motoneuronal cell bodies, not with other cells present in the nucleu
s, i.e., glial or epithelial cells. RT-PCR analysis of unlesioned facial ti
ssue revealed the presence of mRNAs encoding vasopressin V-1a, vasopressin
V-1b and oxytocin receptors, whereas only the V-1a receptor mRNA was found
to be increased following axotomy in the lesioned facial tissue. These data
suggest that the axotomy-induced expression of vasopressin receptors in th
e rat facial nucleus is due, at least to a large extent, to an increase of
the V-1a vasopressin receptor mRNA in facial motoneurons. (C) 1999 Elsevier
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