化学
葡萄糖稳态
肽
氨基酸
二肽
受体
胰高血糖素样肽-1
胰高血糖素
胰高血糖素样肽1受体
体外
胰岛素
生物化学
兴奋剂
激素
药理学
内科学
内分泌学
糖尿病
胰岛素抵抗
2型糖尿病
生物
医学
作者
Claudio Mapelli,Sesha Natarajan,Jean‐Philippe Meyer,Margarita Bastos,Michael S. Bernatowicz,Ving G. Lee,Jelka Pluščec,Douglas J. Riexinger,Ellen Sieber-McMaster,Keith L. Constantine,Constance Smith-Monroy,Rajasree Golla,Zhengping Ma,Daniel Angelo Longhi,Dan Shi,Xin Li,Joseph R. Taylor,Barry Koplowitz,L. Cecilia,Ashish Khanna
摘要
Glucagon-like peptide 1 (GLP-1) is a 30 or 31 amino acid peptide hormone that contributes to the physiological regulation of glucose homeostasis and food intake. Herein, we report the discovery of a novel class of 11 amino acid GLP-1 receptor agonists. These peptides consist of a structurally optimized 9-mer, which is closely related to the N-terminal 9 amino acids of GLP-1, linked to a substituted C-terminal biphenylalanine (BIP) dipeptide. SAR studies resulted in 11-mer GLP-1R agonists with similar in vitro potency to the native 30-mer. Peptides 21 and 22 acutely reduced plasma glucose excursions and increased plasma insulin concentrations in a mouse model of diabetes. These peptides also showed sustained exposures over several hours in mouse and dog models. The described 11-mer GLP-1 receptor agonists represent a new tool in further understanding GLP-1 receptor pharmacology that may lead to novel antidiabetic agents.
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