1. Lansoprazole enhances the antidiabetic effect of sitagliptin in mice with diet-induced obesity and healthy human subjects.
- Author
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Hao S, Sun J, Tian X, Sun X, Zhang Z, and Gao Y
- Subjects
- Adult, Animals, Area Under Curve, Blood Glucose drug effects, C-Peptide blood, Diet adverse effects, Drug Synergism, Drug Therapy, Combination methods, Glucose metabolism, Glucose Tolerance Test methods, Humans, Hypoglycemic Agents pharmacokinetics, Insulin blood, Lansoprazole pharmacokinetics, Male, Mice, Mice, Inbred C57BL, Mice, Obese, Obesity blood, Pyrazines pharmacokinetics, Sitagliptin Phosphate, Triazoles pharmacokinetics, Hypoglycemic Agents pharmacology, Hypoglycemic Agents therapeutic use, Lansoprazole pharmacology, Lansoprazole therapeutic use, Obesity drug therapy, Pyrazines pharmacology, Pyrazines therapeutic use, Triazoles pharmacology, Triazoles therapeutic use
- Abstract
Objectives: Proton pump inhibitors as adjunctive therapy would improve diabetes control and could enhance the hypoglycaemic activity of DPP-4 inhibitors. The aim of the study was to investigate the short-term effects of lansoprazole (LPZ), sitagliptin (SITA) and their combination therapy on glucose regulation and gut peptide secretion., Methods: Glucose and gut peptide were determined and compared after short-term administration of LPZ or SITA, or in combination to mice with diet-induced obesity (DIO) and to healthy human subjects (n = 16) in a 75 g oral glucose tolerance test (OGTT) by a crossover design., Key Findings: In DIO mice, LPZ significantly improve glucose metabolism, increase plasma C-peptide and insulin compared with vehicle treatment. Furthermore, the combination of LPZ and SITA improved glucose tolerance additively, with higher plasma insulin and C-peptide levels compared with SITA-treated mice. Similarly, in human in the OGTT, the combination showed significant improvement in glucose-lowering and insulin increase vs SITA-treated group. However, no significant differences in area under curve (AUC) of insulin, glucose and C-peptide between the LPZ-treated group and baseline, except that mean AUCgastrin was significantly increased by LPZ., Conclusions: LPZ and SITA combination therapy appears to have complementary mechanisms of action and additive antidiabetic effect., (© 2014 Royal Pharmaceutical Society.)
- Published
- 2014
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