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The Journal of Neuroscience, August 1, 1998, 18(15):5565-5574
Expression and Characterization of the Neuropeptide Y
Y5 Receptor Subtype in the Rat Brain
Yvan
Dumont1,
Alain
Fournier2, and
Rémi
Quirion1
1 Douglas Hospital Research Center, Department of
Psychiatry, McGill University, Verdun, Québec, Canada H4H 1R3,
and 2 INRS-Santé, Université du
Québec, Pointe-Claire, Québec, Canada H9R 1G6
The neuropeptide Y Y5 receptor subtype has generated
great interest, especially regarding its possible involvement in
feeding behaviors. However, its distribution and sites of expression in the mammalian brain are, in large part, unknown because of the lack of
selective tools. We demonstrate in this study that specific [125I][Leu31,Pro34]PYY
binding is competed in a biphasic manner by BIBP3226, a Y1 receptor antagonist, demonstrating the existence of sensitive and
insensitive sites to BIBP3226. Assays performed by using
[125I][Leu31,Pro34]PYY
in the presence of 1 µM BIBP3226 to block the
Y1 receptor subtype revealed a pharmacological profile
highly similar to the cloned Y5 receptor. Moreover, results
obtained with GW1229 suggest that the Y4 subtype represents
only a very small proportion of the total population of NPY receptors
in the rat brain. Quantitative receptor autoradiographic data revealed
the discrete distribution of
[125I][Leu31,Pro34]PYY/BIBP3226-insensitive
Y5 sites in the rat brain, with the external plexiform
layer of the olfactory bulb, the lateral septum, the anteroventral
thalamic nucleus, the CA3 subfield of the ventral hippocampus, the
nucleus tractus solitarius, and the area postrema being most enriched.
Rather surprisingly, in the hypothalamus, a key structure modulating
food intake, only low densities of Y5 binding sites were
detected as well as in most other regions of the rat brain. These data
suggest that the Y5 receptor protein is expressed and
translated by a small percentage of hypothalamic neurons and that the
effect of NPY on feeding behaviors likely is mediated by more
than one class of NPY receptors. It also indicates that the
Y5 receptor may be involved in other biological actions induced by NPY. Taken together, these data represent the first pharmacological demonstration of the expression and discrete
localization of the Y5 receptor protein in the rat
brain.
Key words:
NPY/PYY receptor subtypes; Y5 receptor
subtype; rat brain; autoradiographic studies; receptor binding
assays
Copyright © 1998 Society for Neuroscience 0270-6474/98/18155565-10$05.00/0
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