1060-P: The Effect of FGF21/GLP-1 Fusion Protein on Glucose and Lipid Metabolism Using Diabetic Mice Models

Objective: Fibroblast growth factor 21 (FGF-21) is an endocrine factor playing important role in energy metabolic pathways and might be a potential therapeutic target for metabolic disorders such as type 2 diabetes (T2D) and NASH. However, Wild type FGF-21’s clinical application is hindered due to i...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2020-06, Vol.69 (Supplement_1)
Hauptverfasser: GUO, LIXIN, PAN, QI, CHEN, CHAO, LIN, SHUSHAN, LI, YU, LI, XIAOPING, CHEN, XIAOFENG, LIU, LIANG, LI, WENJIA, TANG, XINFA
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Objective: Fibroblast growth factor 21 (FGF-21) is an endocrine factor playing important role in energy metabolic pathways and might be a potential therapeutic target for metabolic disorders such as type 2 diabetes (T2D) and NASH. However, Wild type FGF-21’s clinical application is hindered due to its limited bio-activity. To enhance the medicinal properties, this study mutated FGF-21 to improve its bio-activity. And based on potential synergistic effect of GLP-1 and FGF-21, a FGF-21/GLP-1 fusion protein was constructed to develop a potential T2D/NASH effective drug. Methods: FGF-21-Fc was mutated to enhance its receptor interaction and stability. FGF-21 mutants’ blood glucose reduction capability were compared on db/db mice. Moreover, by constructing a dual agonist from FGF-21 and GLP-1, the bio-activity was further enhanced. Using HFD ob/ob mice, the dual agonist was evaluated by measuring multiple indicators such as blood glucose level, body weight, liver function, and the NAS score. Results: Results from db/db mice (n=9, single SC injection, 40nM/kg) show that the mutated FGF-21-Fc possesses significantly stronger blood glucose lowering effect than the wild type (P
ISSN:0012-1797
1939-327X
DOI:10.2337/db20-1060-P