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Neuropeptide Y5 receptor antagonism does not induce clinically meaningful weight loss in overweight and obese adults

Authors :
Steven B. Heymsfield
Carol Addy
Richard Hargreaves
Bengt Långström
Keith Gottesdiener
Wai-Si Eng
Takehiro Fukami
Priscilla Hollander
Josee Cote
John M. Amatruda
Ira Gantz
Ken Fujioka
Keith D. Kaufman
H. Donald Burns
Ngozi Erondu
Shailaja Suryawanshi
George A. Bray
Sandra M. Sanabria-Bohórquez
Akio Kanatani
Bret J. Musser
Madhuja Mallick
Harold Bays
Douglas J. MacNeil
Source :
Cell Metabolism. (4):275-282
Publisher :
Elsevier Inc.

Abstract

SummaryNeuropeptide Y (NPY) is a potent orexigenic neuropeptide, and antagonism of NPY Y1 and NPY Y5 receptors (NPYxR) is considered a potentially important anti-obesity drug target. We tested the hypothesis that blockade of the NPY5R will lead to weight loss in humans using MK-0557, a potent, highly selective, orally active NPY5R antagonist. The initial series of experiments reported herein, including a multiple-dose positron-emission tomography study and a 12 week proof-of concept/dose-ranging study, suggested an optimal MK-0557 dose of 1 mg/day. The hypothesis was then tested in a 52 week, multicenter, randomized, double-blind, placebo-controlled trial involving 1661 overweight and obese patients. Although statistically significant at 52 weeks, the magnitude of induced weight loss was not clinically meaningful. These observations provide the first clinical insight into the human NPY-energy homeostatic pathway and suggest that solely targeting the NPY5R in future drug development programs is unlikely to produce therapeutic efficacy.

Details

Language :
English
ISSN :
15504131
Issue :
4
Database :
OpenAIRE
Journal :
Cell Metabolism
Accession number :
edsair.doi.dedup.....675f19caa9b8aedab98b542e250f3a02
Full Text :
https://doi.org/10.1016/j.cmet.2006.08.002