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The fatty acid conjugated exendin-4 analogs for type 2 antidiabetic therapeutics

2010; Elsevier BV; Volume: 144; Issue: 1 Linguagem: Inglês

10.1016/j.jconrel.2010.01.024

1873-4995

Su Young Chae, Yang Gyu Choi, Sohee Son, Sung Youb Jung, Doo Sung Lee, Kang Choon Lee,

Metabolism, Diabetes, and Cancer

Improved glucagon-like peptide-1 (GLP-1) receptor activation is considered one of the most effective targets for antidiabetic therapy. For this purpose, we modified the GLP-1 analog of exendin-4 using two fatty acids (FA) either lauric acid (LUA, C12) or palmitic acid (PAA, C16) at its two lysine residues, to produce; Lys12-FA-Exendin-4 (FA-M2), Lys27-FA-Exendin-4 (FA-M1), or Lys12,27-diBA-Exendin-4 (FA-Di). The structural, biological, and pharmaceutical characteristics of these exendin-4 analogs were then investigated. Biological activity tests demonstrated that LUA-M1 had well-preserved in vivo antidiabetic activity and in vitro insulinotropic activity with minimum GLP-1 receptor binding affinity loss as compared with exendin-4. Furthermore, pharmacokinetic studies in rats revealed that s.c. administration of LUA-M1 significantly enhanced pharmacokinetic parameters, such as, elimination half-life, mean residence time, and AUC values as compared with exendin-4. The protracted antidiabetic effects of LUA-M1 were also confirmed by prolonged normoglycemia observed in type 2 diabetic mice (20 nmol/mouse single injection of exendin-4 or LUA-M1 induced normoglycemia for 6 or 24 h, respectively). These findings suggest that FA conjugated exendin-4s should be considered potential candidates for the treatment of diabetes.