Differential inhibition of sildenafil and macitentan on saxagliptin metabolism

• Published in: Toxicology and applied pharmacology 2024-05, Vol.486, p.116934-116934, Article 116934
• Main Authors: Dai, Ge-xin, Tan, Wei, Shen, Yuxin, Lin, Dongdong, Xu, Ren-ai, Lin, Qianmeng, Wei, Zhen
• Format: Article
• Language: English
• Subjects: CYP3A4; Drug-Drug Interaction; Macitentan; Molecular Docking; Saxagliptin; Sildenafil
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2024.116934

The development of diabetes mellitus (DM) is generally accompanied by erectile dysfunction (ED) and pulmonary arterial hypertension (PAH), which increases the use of combination drug therapy and the risk of drug-drug interactions. Saxagliptin for the treatment of DM, sildenafil for the treatment of ED and PAH, and macitentan for the treatment of PAH are all substrates of CYP3A4, which indicates their potential involvement in drug-drug interactions. Therefore, we investigated potential pharmacokinetic interactions between saxagliptin and sildenafil/macitentan. We investigated this speculation both in vitro and in vivo, and explored the underlying mechanism using in vitro hepatic metabolic models and molecular docking assays. The results showed that sildenafil substantially inhibited the metabolism of saxagliptin by occupying the catalytic site of CYP3A4 in a competitive manner, leading to the alterations in the pharmacokinetic properties of saxagliptin in terms of increased maximum plasma concentration (Cmax), area under the plasma concentration–time curve from time 0 to 24 h (AUC(0-t)), area under the plasma concentration–time curve from time 0 extrapolated to infinite time (AUC(0-∞)), decreased clearance rate (CLz/F), and prolonged terminal half-life (t1/2). In contrast, a slight inhibition was observed in saxagliptin metabolism when concomitantly used with macitentan, as no pharmacokinetic parameters were altered, except for CLz/F. Thus, dosage adjustment of saxagliptin may be required in combination with sildenafil to achieve safe therapeutic plasma concentrations and reduce the risk of potential toxicity, but it is not necessary for co-administration with macitentan. •Sildenafil substantially inhibited the metabolism of saxagliptin.•The mechanism of inhibition of saxagliptin by sildenafil was in a competitive manner.•Sildenafil significantly improve the bioavailability of saxagliptin in rats.