D. Bodie et al., ORGANIZATION, DEVELOPMENT, AND EFFECTS OF INFRAORBITAL NERVE TRANSECTION ON GALANIN BINDING-SITES IN THE TRIGEMINAL BRAIN-STEM COMPLEX, Somatosensory & motor research, 14(3), 1997, pp. 168-180
Previous experiments from this laboratory have indicated that transect
ion of the infraorbital nerve (ION, the trigeminal [V] branch that sup
plies the mystacial vibrissae follicles) at birth and in adulthood has
markedly different effects on galanin immunoreactivity in the V brain
stem complex. Adult nerve transection increases galanin immunoreactivi
ty in the superficial layers of V subnucleus caudalis (SpC) only, whil
e neonatal nerve transection results in increased galanin expression i
n vibrissae-related primary afferents throughout the V brainstem compl
ex. The present study describes the distribution of binding sites for
this peptide in the mature and developing V ganglion and brainstem com
plex and determines the effects of neonatal and adult ION damage and t
he associated changes in galanin levels upon their distribution and de
nsity. Galanin binding sites are densely distributed in all V brainste
m subnuclei and are particularly dense in V subnucleus interpolaris an
d the superficial layers of SpC. They are present at birth (P-0) and t
heir distribution is similar to that in adult animals. Transection of
the ION in adulthood and examination of brainstem 7 days later indicat
ed marked reductions in the density of galanin binding sites in the V
brainstem complex. With the exception of the superficial laminae of Sp
C, the same reduction in density remained apparent in rats that surviv
ed >45 days after nerve cuts. Transection of the ION on P-0 resulted i
n no change in the density of galanin binding sires in the brainstem a
fter either 7 or > 60 days survival. These results indicate that dense
ly distributed galanin binding sites are present in the V brainstem co
mplex of both neonatal and adult rats, that they are located in region
s not innervated by galanin-positive axons, and that their density is
not significantly influenced by large lesion-induced changes in the pr
imary afferent content of their natural ligand.