Orexin-induced food intake involves neuropeptide Y pathway

Citation
A. Yamanaka et al., Orexin-induced food intake involves neuropeptide Y pathway, BRAIN RES, 859(2), 2000, pp. 404-409
Citations number
25
Categorie Soggetti
Neurosciences & Behavoir
Journal title
BRAIN RESEARCH
ISSN journal
00068993 → ACNP
Volume
859
Issue
2
Year of publication
2000
Pages
404 - 409
Database
ISI
SICI code
0006-8993(20000324)859:2<404:OFIINY>2.0.ZU;2-E
Abstract
Orexins (orexin-A and -B) are recently identified neuropeptides, which are thought to be implicated in the regulation of feeding behavior. We used a N PY-Y1 receptor specific antagonist, BIB03304, to examine whether NPY is inv olved in orexin-induced feeding behavior. Intracerebroventricular administr ation of orexin-A (10 nmol) induced food intake in rats (food intake for 3 h; vehicle 0.3 +/- 0.2 g vs. orexin-A 10 nmol, 4.0 +/- 0.5 g, n = 4). Orexi n-induced feeding behavior was partially inhibited by prior administration of BIB03304 (3 h food intake: orexin-A 10 nmol, 4.0 +/- 0.5 g vs. BIB03304 (60 mu g) + orexin-A 10 nmol, 2.2 +/- 0.2 g, n = 4). A low dose of BIB03304 (30 mu g) did not show a significant inhibitory effect. BIB03457, an inact ive enantiomer, used as a negative control, did not show any inhibitory eff ect on orexin-A-induced feeding behavior. Fos expression was observed in NP Y-containing neurons in the arcuate nucleus 1 h after orexin-A (10 nmol) wa s administered intracerebroventricularly (control 0.3 +/- 0.08%, orexin-A 1 0.2 +/- 0.8%, n = 5 rats/group). These observations suggest that NPY is inv olved in orexin-induced feeding behavior. However, BIB03304 did not complet ely abolish the effect of orexin-A. These results suggest that orexin-A eli cits feeding behavior partially via the NPY pathway. The NPY system could b e the one of downstream pathways by which orexin-A induces feeding behavior . Another pathway may also be involved in orexin-A-induced feeding behavior , because BIB03304 did not completely abolish orexin-A-induced feeding beha vior. (C) 2000 Published by Elsevier Science B.V. All rights reserved.