Lansoprazole enhances the antidiabetic effect of sitagliptin in mice with diet-induced obesity and healthy human subjects

被引:11
作者
Hao, ShaoJun [1 ]
Sun, JianHua [1 ]
Tian, Xikui [2 ]
Sun, Xu [3 ]
Zhang, ZhenXing [3 ]
Gao, Yuan [3 ]
机构
[1] 371 Hosp PLA, Dept Pharm & Equipment, Xinxiang, Peoples R China
[2] 371 Hosp PLA, Dept Cardiol, Xinxiang, Peoples R China
[3] Jinan Mil Area, Inst Drug & Instrument Control, Jinan, Peoples R China
关键词
biopharmaceutics and drug disposition; drug disposition in tissues and whole animals; in-vivo/in-vitro correlation; pharmacokinetics and drug disposition; PROTON PUMP INHIBITOR; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; IMPROVES GLYCEMIC CONTROL; PANCREATIC-DUCT CELLS; COMBINATION THERAPY; DOUBLE-BLIND; RESTORES NORMOGLYCEMIA; INSULIN-SECRETION; GROWTH-FACTOR; GASTRIN;
D O I
10.1111/jphp.12237
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 AUC(gastrin) was significantly increased by LPZ. Conclusions LPZ and SITA combination therapy appears to have complementary mechanisms of action and additive antidiabetic effect.
引用
收藏
页码:1133 / 1139
页数:7
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