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Neuropeptide Y5 receptor antagonism does not induce clinically meaningful weight loss in overweight and obese adults
- 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.
- Subjects :
- Adult
medicine.medical_specialty
Adolescent
Physiology
HUMDISEASE
Neuropeptide
Administration, Oral
Pharmacology
Overweight
Sensitivity and Specificity
MOLNEURO
Placebos
Structure-Activity Relationship
Double-Blind Method
Weight loss
Cyclohexanes
Internal medicine
Orexigenic
Medicine
Humans
Spiro Compounds
Obesity
Receptor
Molecular Biology
Aged
Dose-Response Relationship, Drug
Molecular Structure
business.industry
Body Weight
Antagonist
Cell Biology
Middle Aged
Neuropeptide Y receptor
Blockade
Receptors, Neuropeptide Y
Endocrinology
Treatment Outcome
CHEMBIO
Positron-Emission Tomography
Pyrazoles
Anti-Obesity Agents
medicine.symptom
business
medicine.drug
Subjects
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