In vitro assessment of the risk of ABCB1-mediated drug–drug interaction between rivaroxaban and tacrolimus in human embryonic kidney 293 recombinant cell lines

IF 3.4 3区 医学 Q2 HEMATOLOGY Research and Practice in Thrombosis and Haemostasis Pub Date : 2024-07-01 DOI:10.1016/j.rpth.2024.102521
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Abstract

Background

In lung transplant patients, direct oral anticoagulants are often taken in combination with immunosuppressive drugs such as tacrolimus. Since tacrolimus is a substrate and inhibitor of the efflux protein ABCB1, also transporting direct oral anticoagulants, a possible drug–drug interaction mediated by competition for this transporter needs to be investigated.

Objectives

To determine the in vitro effect of tacrolimus on ABCB1-mediated rivaroxaban transport in order to support clinician practice.

Methods

Recombinant cell line models, based on human embryonic kidney 293 cells, were generated by a stable transfection process to overexpress ABCB1 or not (control cells). The impact of tacrolimus on ABCB1-mediated rivaroxaban transport was assessed by accumulation experiments.

Results

ABCB1 expression decreased the cellular accumulation of rivaroxaban and tacrolimus at their respective clinically relevant concentrations when compared with control cells. This confirms the involvement of ABCB1 in the active transport of tacrolimus and rivaroxaban. However, tacrolimus had no significant influence on rivaroxaban disposition at those clinically relevant concentrations.

Conclusion

Our study does not provide evidence for a possible interaction between tacrolimus and rivaroxaban when used together in practice.

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体外评估利伐沙班和他克莫司在 HEK293 重组细胞系中 ABCB1 介导的药物相互作用风险
背景在肺移植患者中,直接口服抗凝剂通常与免疫抑制剂(如他克莫司)联合使用。由于他克莫司是外排蛋白 ABCB1 的底物和抑制剂,而 ABCB1 也能转运直接口服抗凝药,因此需要研究通过竞争该转运体而介导的可能的药物相互作用。方法以人类胚胎肾脏 293 细胞为基础,通过稳定的转染过程产生过表达 ABCB1 或不表达 ABCB1(对照细胞)的重组细胞系模型。结果与对照细胞相比,ABCB1 的表达降低了利伐沙班和他克莫司在各自的临床相关浓度下的细胞蓄积。这证实了 ABCB1 参与了他克莫司和利伐沙班的主动转运。结论:我们的研究没有提供证据表明他克莫司和利伐沙班在实际中同时使用时可能会发生相互作用。
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来源期刊
CiteScore
5.60
自引率
13.00%
发文量
212
审稿时长
7 weeks
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