Safer Medicines Trust, Kingsbridge, UK.
Mechanistic Safety and Disposition, IVIVT, GlaxoSmithKline, Ware, Hertfordshire, UK.
Clin Pharmacol Ther. 2018 Nov;104(5):916-932. doi: 10.1002/cpt.1222.
Bile salt export pump (BSEP) inhibition has emerged as an important mechanism that may contribute to the initiation of human drug-induced liver injury (DILI). Proactive evaluation and understanding of BSEP inhibition is recommended in drug discovery and development to aid internal decision making on DILI risk. BSEP inhibition can be quantified using in vitro assays. When interpreting assay data, it is important to consider in vivo drug exposure. Currently, this can be undertaken most effectively by consideration of total plasma steady state drug concentrations (C ). However, because total drug concentrations are not predictive of pharmacological effect, the relationship between total exposure and BSEP inhibition is not causal. Various follow-up studies can aid interpretation of in vitro BSEP inhibition data and may be undertaken on a case-by-case basis. BSEP inhibition is one of several mechanisms by which drugs may cause DILI, therefore, it should be considered alongside other mechanisms when evaluating possible DILI risk.
胆汁盐输出泵 (BSEP) 抑制已成为一种重要的机制,可能导致人类药物性肝损伤 (DILI) 的发生。在药物发现和开发过程中,建议主动评估和了解 BSEP 抑制作用,以帮助内部做出关于 DILI 风险的决策。可以使用体外测定法来定量 BSEP 抑制作用。在解释测定数据时,重要的是要考虑体内药物暴露情况。目前,这可以通过考虑总血浆稳态药物浓度 (C ) 来最有效地进行。但是,由于总药物浓度不能预测药理作用,因此总暴露量与 BSEP 抑制作用之间没有因果关系。各种后续研究可以帮助解释体外 BSEP 抑制数据,并且可以根据具体情况进行。BSEP 抑制是药物引起 DILI 的几种机制之一,因此,在评估可能的 DILI 风险时,应与其他机制一起考虑。