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
{"title":"In vitro assessment of the risk of ABCB1-mediated drug–drug interaction between rivaroxaban and tacrolimus in human embryonic kidney 293 recombinant cell lines","authors":"","doi":"10.1016/j.rpth.2024.102521","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Objectives</h3><p>To determine the <em>in vitro</em> effect of tacrolimus on ABCB1-mediated rivaroxaban transport in order to support clinician practice.</p></div><div><h3>Methods</h3><p>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.</p></div><div><h3>Results</h3><p>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.</p></div><div><h3>Conclusion</h3><p>Our study does not provide evidence for a possible interaction between tacrolimus and rivaroxaban when used together in practice.</p></div>","PeriodicalId":20893,"journal":{"name":"Research and Practice in Thrombosis and Haemostasis","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2475037924002164/pdfft?md5=4bec598e07edbcc379d704c378e999c9&pid=1-s2.0-S2475037924002164-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research and Practice in Thrombosis and Haemostasis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2475037924002164","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

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.

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.60
自引率
13.00%
发文量
212
审稿时长
7 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信