Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina, USA.
Brock Scientific Consulting, LLC, Montgomery Village, Maryland, USA.
Clin Pharmacol Ther. 2021 Feb;109(2):433-442. doi: 10.1002/cpt.2007. Epub 2020 Sep 8.
Patients with autosomal dominant polycystic kidney disease (ADPKD) exhibit enhanced susceptibility to tolvaptan hepatotoxicity relative to other patient populations. In a rodent model of ADPKD, the expression and function of the biliary efflux transporter Mrp2 was reduced, and biliary excretion of a major tolvaptan metabolite (DM-4103) was decreased. The current study investigated whether reduced biliary efflux could contribute to increased susceptibility to tolvaptan-associated hepatotoxicity using a quantitative systems toxicology (QST) model (DILIsym). QST simulations revealed that decreased biliary excretion of DM-4103, but not tolvaptan, resulted in substantial hepatic accumulation of bile acids, decreased electron transport chain activity, reduced hepatic adenosine triphosphate concentrations, and an increased incidence of hepatotoxicity. In vitro experiments (C-DILI) with sandwich-cultured human hepatocytes and HepaRG cells were performed to assess tolvaptan-associated hepatotoxic effects when MRP2 was impaired by chemical inhibition (MK571, 50 µM) or genetic knockout, respectively. Tolvaptan (64 µM, 24-hour) treatment of these cells increased cytotoxicity markers up to 27.9-fold and 1.6-fold, respectively, when MRP2 was impaired, indicating that MRP2 dysfunction may be involved in tolvaptan-associated cytotoxicity. In conclusion, QST modeling supported the hypothesis that reduced biliary efflux of tolvaptan and/or DM-4103 could account for increased susceptibility to tolvaptan-associated hepatotoxicity; in vitro experiments implicated MRP2 dysfunction as a key factor in susceptibility. QST simulations revealed that DM-4103 may contribute to hepatotoxicity more than the parent compound. ADPKD progression and gradual reduction in MRP2 activity may explain why acute liver events can occur well after one year of tolvaptan treatment.
常染色体显性遗传多囊肾病(ADPKD)患者对托伐普坦的肝毒性比其他患者群体更敏感。在 ADPKD 的啮齿动物模型中,胆汁流出转运体 Mrp2 的表达和功能降低,托伐普坦的主要代谢物(DM-4103)的胆汁排泄减少。本研究使用定量系统毒理学(QST)模型(DILIsym)研究了减少胆汁流出是否会导致对托伐普坦相关肝毒性的易感性增加。QST 模拟表明,DM-4103 而非托伐普坦的胆汁排泄减少会导致大量胆汁酸在肝脏中蓄积、电子传递链活性降低、肝三磷酸腺苷浓度降低和肝毒性发生率增加。通过夹心培养的人肝细胞和 HepaRG 细胞进行体外实验(C-DILI),分别评估 MRP2 被化学抑制(MK571,50µM)或基因敲除抑制时托伐普坦相关肝毒性的影响。当 MRP2 功能障碍时,这些细胞中托伐普坦(64µM,24 小时)处理会导致细胞毒性标志物增加高达 27.9 倍和 1.6 倍,表明 MRP2 功能障碍可能与托伐普坦相关的细胞毒性有关。总之,QST 模型支持这样的假设,即托伐普坦和/或 DM-4103 的胆汁排泄减少可能导致对托伐普坦相关肝毒性的易感性增加;体外实验表明 MRP2 功能障碍是易感性的关键因素。QST 模拟表明,DM-4103 可能比母体化合物更易导致肝毒性。ADPKD 的进展和 MRP2 活性的逐渐降低可能解释了为什么在托伐普坦治疗一年后才会发生急性肝事件。