Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill.
Toxicol Sci. 2014 May;139(1):99-107. doi: 10.1093/toxsci/kfu033. Epub 2014 Feb 22.
Drug-induced phospholipidosis (PLD) is characterized by phospholipid accumulation within the lysosomes of affected tissues, resulting in lysosomal enlargement and laminar body inclusions. Numerous adverse effects and toxicities have been linked to PLD-inducing drugs, but it remains unknown whether drug-induced PLD represents a distinct toxicity or cellular adaptation. In silico and immortalized cellular models have been used to evaluate the PLD potential of new drugs, but these systems have some limitations. The aims of this study were to determine whether primary sandwich-cultured hepatocytes (SCH) can serve as a sensitive and selective model to evaluate hepatic drug-induced PLD, and to evaluate the impact of PLD on the uptake and biliary excretion of probe substrates, taurocholate (TC) and rosuvastatin (RSV). Rat SCH were cultured for 48 h with prototypic hepatic PLD-inducing drugs, amiodarone (AMD), chloroquine (CHQ), desipramine (DES), and azithromycin (AZI), as well as the renal PLD inducer gentamicin (GTM). LysoTracker Red localization and transmission electron microscopy indicated enlarged lysosomal compartments and laminar body inclusions in SCH treated with AMD, CHQ, DES, and AZI, but not GTM, relative to control. PLD resulted in a 51-92% decrease in the in vitro biliary clearance of both TC and RSV; the biliary excretion index significantly decreased for TC from 88 to 35-73%. These data suggested that PLD significantly reduced both organic anion transporting polypeptide-mediated uptake, and bile salt export pump-mediated biliary transport processes. The current study demonstrates that the rat SCH system is a promising model to study hepatic PLD in vitro. Altered hepatic transport of anionic substrates secondary to drug-induced PLD is a novel finding.
药物诱导的磷脂病(PLD)的特征是受影响组织的溶酶体中磷脂的积累,导致溶酶体增大和层状体包含物。许多不良反应和毒性与诱导 PLD 的药物有关,但尚不清楚药物诱导的 PLD 是否代表一种独特的毒性或细胞适应。已经使用了计算机模拟和永生化细胞模型来评估新药的 PLD 潜力,但这些系统存在一些局限性。本研究的目的是确定原代三明治培养的肝细胞(SCH)是否可以作为评估肝药物诱导 PLD 的敏感和选择性模型,以及评估 PLD 对探针底物牛磺胆酸钠(TC)和瑞舒伐他汀(RSV)摄取和胆汁排泄的影响。将大鼠 SCH 用典型的肝 PLD 诱导药物胺碘酮(AMD)、氯喹(CHQ)、去甲丙咪嗪(DES)和阿奇霉素(AZI)以及肾 PLD 诱导剂庆大霉素(GTM)培养 48 小时。与对照相比,用 AMD、CHQ、DES 和 AZI 处理的 SCH 中,溶酶体定位和透射电子显微镜显示溶酶体腔增大和层状体包含物。PLD 导致 TC 和 RSV 的体外胆汁清除率分别降低 51-92%;TC 的胆汁排泄指数从 88 显著降低至 35-73%。这些数据表明,PLD 显著降低了有机阴离子转运蛋白介导的摄取和胆汁盐输出泵介导的胆汁转运过程。本研究表明,大鼠 SCH 系统是研究体外肝 PLD 的有前途的模型。药物诱导的 PLD 导致阴离子底物的肝转运改变是一个新发现。