H. Herbert et G. Flugge, DISTRIBUTION OF ALPHA(2)-ADRENERGIC BINDING-SITES IN THE PARABRACHIALCOMPLEX OF THE RAT, Anatomy and embryology, 192(6), 1995, pp. 507-516
The present study describes the distribution of alpha(2)-adrenoceptors
in the parabrachial and Kolliker-Fuse nucleus of the rat by employing
the tritium-labeled alpha(2)-receptor antagonist rauwolscine ([H-3]-R
AUW) as a ligand. The [H-3]-RAUW binding was densitometrically quantif
ied in five nuclei of the parabrachial (PB) complex in serial coronal
sections. We found that cytoarchitectonically and anatomically distinc
t nuclei of the PB complex exhibit different numbers of [H-3]-RAUW-bin
ding sites. The largest number of binding sites was observed over the
external lateral PB and caudally over the waist area of the PB. Lower
numbers of binding sites were found in the remaining lateral PB nuclei
, followed by the medial PB and the Kolliker-Fuse nucleus. In addition
we disclosed that the internal lateral PB contains a very low number
of binding sites while the external medial PB is marked by dense [H-3]
-RAUW binding. Also, the affinities of the binding sites differed betw
een the PB areas. High affinities were observed in the external latera
l PB, the remaining lateral PB nuclei and in the waist area of the PB,
while the medial PB and the Kolliker-Fuse nucleus exhibited only low
affinities for the ligand. Furthermore, saturation curves demonstrated
non-linear profiles, indicating the presence of more than one populat
ion of binding sites in the PB nuclei for the radioligand. Our data de
monstrate that the PB exhibits a distinct distribution of alpha(2)-adr
energic binding sites. These correlate well with the cytoarchitectonic
ally defined nuclei of the PB complex and with the pattern of ascendin
g axons from the medial nucleus of the solitary tract and the area pos
trema terminating in the PB. Since a large number of these projection
neurons utilize adrenaline or noradrenaline as their transmitters, we
conclude that solitary-parabrachial neurotransmission to the fore-brai
n is, at least in part, mediated via alpha(2)-adrenoceptors. -