Effect of Ranitidine on the Pharmacokinetic and Pharmacodynamic Profile of Metformin in Rabbits

Abstract

Background: The aim of this study was to investigate the effect of ranitidine, an H2-receptor antagonist, on the
pharmacokinetics of metformin, a widely used antidiabetic drug in albino rabbits. Methods: Albino rabbits were
divided into 3 groups, group I received metformin alone, group II received ranitidine alone, and group III received
ranitidine 30 minutes prior to metformin. Blood samples were collected at various intervals post-administration
for the estimation of blood glucose levels and metformin concentration. Results: The study found that the plasma
metformin concentrations (CMet) were below the limit of quantification at 8 hours in group I, indicating a near
complete elimination of the drug from systemic circulation. However, quantifiable levels of metformin were
observed at 8 hours in group III, suggesting a significant increase in the mean residence time of the molecule
caused by a decrease in metformin elimination. The study also found that the area under the curve of metformin
was significantly increased by ranitidine pre-treatment in group III, suggesting an increase in systemic exposure
to metformin. Conclusion: This study suggests that concomitant administration of ranitidine and metformin in
rabbits leads to an increase in the mean residence time of metformin due to the inhibition of the organic cation
transporter 1 by ranitidine, resulting in an increase in systemic exposure to metformin. The study highlights the
potential for drug-drug interactions between ranitidine and metformin, which may impact the efficacy and safety
of metformin treatment. Further studies in humans are needed to confirm these findings.