Susukida Takeshi, Sekine Shuichi, Nozaki Mayuka, Tokizono Mayuko, Ito Kousei
Laboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Chiba University, Chuo-ku, Chiba, Japan.
Laboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Chiba University, Chuo-ku, Chiba, Japan
Drug Metab Dispos. 2015 Nov;43(11):1760-8. doi: 10.1124/dmd.115.065425. Epub 2015 Sep 1.
Drug-induced liver injury (DILI) is of concern to the pharmaceutical industry, and reliable preclinical screens are required. Previously, we established an in vitro bile acid-dependent hepatotoxicity assay that mimics cholestatic DILI in vivo. Here, we confirmed that this assay can predict cholestatic DILI in clinical situations by comparing in vitro cytotoxicity data with in vivo risk. For 38 drugs, the frequencies of abnormal increases in serum alkaline phosphatase (ALP), transaminases, gamma glutamyltranspeptidase (γGT), and bilirubin were collected from interview forms. Drugs with frequencies of serum marker increases higher than 1% were classified as high DILI risk compounds. In vitro cytotoxicity was assessed by monitoring lactate dehydrogenase release from rat and human sandwich-cultured hepatocytes (SCRHs and SCHHs) incubated with the test drugs (50 μM) for 24 hours in the absence or presence of a bile acids mixture. Receiver operating characteristic analyses gave optimal cutoff toxicity values of 19.5% and 9.2% for ALP and transaminases in SCRHs, respectively. Using this cutoff, high- and low-risk drugs were separated with 65.4-78.6% sensitivity and 66.7-79.2% specificity. Good separation was also achieved using SCHHs. In conclusion, cholestatic DILI risk can be successfully predicted using a sandwich-cultured hepatocyte-based assay.
药物性肝损伤(DILI)是制药行业关注的问题,需要可靠的临床前筛选方法。此前,我们建立了一种体外胆汁酸依赖性肝毒性测定法,该方法可模拟体内胆汁淤积性DILI。在此,我们通过将体外细胞毒性数据与体内风险进行比较,证实了该测定法可预测临床情况下的胆汁淤积性DILI。对于38种药物,从访谈表格中收集血清碱性磷酸酶(ALP)、转氨酶、γ-谷氨酰转肽酶(γGT)和胆红素异常升高的频率。血清标志物升高频率高于1%的药物被归类为高DILI风险化合物。在不存在或存在胆汁酸混合物的情况下,将受试药物(50μM)与大鼠和人夹心培养肝细胞(SCRHs和SCHHs)孵育24小时,通过监测乳酸脱氢酶释放来评估体外细胞毒性。受试者工作特征分析得出,SCRHs中ALP和转氨酶的最佳截断毒性值分别为19.5%和9.2%。使用该截断值,高风险和低风险药物的分离灵敏度为65.4 - 78.6%,特异性为66.7 - 79.2%。使用SCHHs也实现了良好的分离。总之,基于夹心培养肝细胞的测定法可以成功预测胆汁淤积性DILI风险。