| Literature DB >> 28626523 |
Naoki Nishizawa1, Ayumu Niida1, Yasushi Masuda1, Satoshi Kumano1, Kotaro Yokoyama1, Hideki Hirabayashi1, Nobuyuki Amano1, Tetsuya Ohtaki1, Taiji Asami1.
Abstract
Gastrointestinal peptides such as peptide YY (PYY) can regulate appetite, which is relevant to the study of obesity. The intraperitoneal bolus administration of PYY3-36 and a 12-amino acid PYY analogue, benzoyl-[Cha27,28,36,Aib31]PYY25-36 (1), showed similar anorectic activity by activating the Y2 receptor (Y2R). However, food intake inhibition and body weight loss were not observed upon continuous subcutaneous administration of 1 with osmotic pumps in diet-induced obese (DIO) mice. N-Terminal elongation of 1, together with amino acid substitution at position 24, led to a hydrophilic 14-amino acid peptide, Ac-[d-Hyp24,Cha27,28,36,Aib31]PYY23-36 (18), that showed higher affinity and more potent agonist activity for Y2R and a robust anorectic activity with potency similar to that of PYY3-36. In addition, the continuous subcutaneous administration of 18 at 0.3 mg/(kg·day) induced significant body weight loss in DIO mice. These results suggest that a short-length PYY analogue can be a lead compound for antiobesity therapy in a sustained-release formulation.Entities:
Keywords: Anorectic effect; Antiobesity; Peptide YY (PYY); Short-length PYY analogue; Y2 receptor (Y2R)
Year: 2017 PMID: 28626523 PMCID: PMC5467190 DOI: 10.1021/acsmedchemlett.7b00047
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345