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A Long-Acting PYY 3-36 Analog Mediates Robust Anorectic Efficacy with Minimal Emesis in Nonhuman Primates.
- Source :
-
Cell metabolism [Cell Metab] 2019 Apr 02; Vol. 29 (4), pp. 837-843.e5. Date of Electronic Publication: 2019 Feb 14. - Publication Year :
- 2019
-
Abstract
- The gut hormone PYY <subscript>3-36</subscript> reduces food intake in humans and exhibits at least additive efficacy in combination with GLP-1. However, the utility of PYY analogs as anti-obesity agents has been severely limited by emesis and rapid proteolysis, a profile similarly observed with native PYY <subscript>3-36</subscript> in obese rhesus macaques. Here, we found that antibody conjugation of a cyclized PYY <subscript>3-36</subscript> analog achieved high NPY2R selectivity, unprecedented in vivo stability, and gradual infusion-like exposure. These properties permitted profound reduction of food intake when administered to macaques for 23 days without a single emetic event in any animal. Co-administration with the GLP-1 receptor agonist liraglutide for an additional 5 days further reduced food intake with only one animal experiencing a single bout of emesis. This antibody-conjugated PYY analog therefore may enable the long-sought potential of GLP-1/PYY-based combination treatment to achieve robust, well-tolerated weight reduction in obese patients.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
CHO Cells
Cricetulus
Glucagon-Like Peptide-1 Receptor agonists
Glucagon-Like Peptide-1 Receptor metabolism
HEK293 Cells
Humans
Liraglutide pharmacology
Macaca mulatta
Mice
Mice, Inbred C57BL
Obesity drug therapy
Obesity metabolism
Peptide YY administration & dosage
Anorexia chemically induced
Peptide YY chemistry
Peptide YY pharmacology
Vomiting chemically induced
Subjects
Details
- Language :
- English
- ISSN :
- 1932-7420
- Volume :
- 29
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 30773465
- Full Text :
- https://doi.org/10.1016/j.cmet.2019.01.017