Canagliflozin has a robust inhibitory effect on
sodium glucose transporter (SGLT)-2 and a mild inhibitory effect on SGLT1. The main purpose of this study was to investigate the effect of
canagliflozin on circulating active
glucagon-like peptide 1 (GLP-1) levels in patients with
type 2 diabetes. Patients were randomly divided into a control group (n =15) and a
canagliflozin-treated group (n =15). After hospitalization, the
canagliflozin-treated group took 100 mg/day
canagliflozin for the entire study, and after 3 days both groups took 20 mg/day
teneligliptin for an additional 3 days. In a meal test,
canagliflozin significantly decreased the area under curve (AUC) (0-120 min) for plasma
glucose (PG) after 3 days when compared with that at baseline, and addition of
teneligliptin to the
canagliflozin-treated group further decreased it. A significant decrease in the AUC (0-120 min) for serum
insulin by
canagliflozin was obtained, but the addition of
teneligliptin elevated the AUC, and thus abolished the significant difference from baseline. A significant increase in the AUC (0-120 min) of plasma active
GLP-1 by
canagliflozin-treatment compared with that at baseline was observed, and the addition of
teneligliptin resulted in a further increase. However,
canagliflozin-treatment did not change the AUC (0-120 min) of plasma active
glucose-dependent insulinotropic peptide (GIP). In conclusions,
canagliflozin-administration before meals decreased PG and serum
insulin, and increased plasma active
GLP-1 levels in patients with
type 2 diabetes.
Canagliflozin did not greatly influence plasma active GIP levels.