Combination of omeprazole with GLP-1 agonist therapy improves insulin sensitivity and antioxidant activity in liver in type 1 diabetic mice

Pharmacol Rep. 2013;65(4):927-36. doi: 10.1016/s1734-1140(13)71074-0.

Abstract

Background: Combination with suitable pharmacological agents can improve the antiobesity and antidiabetic actions of glucagon like peptide-1 (GLP-1) based therapies. GLP-1 agonist exendin-4 may have insulin-independent effects on amelioration of insulin resistance and hepatic steatosis by virtue of its action on hepatic GLP-1 receptors, and these effects can be improved by combination with proton pump inhibitors. However, it was not assessed whether omeprazole can improve the peripheral actions of exendin-4 in the state of insulin deficiency.

Methods: We investigated the effects of combination of omeprazole with GLP-1 agonist exendin-4 in multiple low-dose streptozotocin (STZ)-induced diabetes in C57BL/KsJ mice, a model of type 1 diabetes. Male diabetic mice were treated with exendin-4 and/or omeprazole for a period of 4 weeks.

Results: Omeprazole treatment had no significant effect on lowering the blood glucose levels of diabetic mice, when compared to control, although it improved the antihyperglycemic actions of exendin-4. Similarly, serum triglycerides and total cholesterols levels were significantly lower in the combination treated mice compared to either exendin-4 and omeprazole alone. In addition, the combination treatment significantly ameliorated lipid peroxidation and hepatic triglycerides in diabetic mice compared to either exendin-4 and omeprazole alone. The improvement in hepatic insulin sensitivity, as indicated by insulin tolerance test (ITT) and pyruvate tolerance test (IPPTT), was correlated with the expression of nuclear factor erythroid-related factor 2 (Nrf2) and insulin receptor substrate-1 (IRS-1) and the combination treatment significantly improved the insulin sensitivity in comparison to vehicle control.

Conclusion: We conclude that combination with omeprazole improves the insulin sensitizing actions of GLP-1 therapy and these effects are partially mediated through the decrease in hepatic steatosis and improvement in antioxidant status in the liver.

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Blood Glucose / drug effects
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / metabolism*
  • Drug Therapy, Combination
  • Exenatide
  • Glucagon-Like Peptide 1 / agonists*
  • Hypoglycemic Agents / pharmacology
  • Hypoglycemic Agents / therapeutic use
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Mice
  • NF-E2-Related Factor 2 / metabolism
  • Omeprazole / pharmacology*
  • Omeprazole / therapeutic use
  • Peptides / pharmacology*
  • Peptides / therapeutic use
  • Proton Pump Inhibitors / pharmacology
  • Proton Pump Inhibitors / therapeutic use
  • Venoms / pharmacology*
  • Venoms / therapeutic use

Substances

  • Antioxidants
  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • NF-E2-Related Factor 2
  • Peptides
  • Proton Pump Inhibitors
  • Venoms
  • Glucagon-Like Peptide 1
  • Exenatide
  • Omeprazole