Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Drug Chem Toxicol. 2019 Nov;42(6):615-623. doi: 10.1080/01480545.2018.1459668. Epub 2018 May 3.
Drug-induced liver injury is a major concern in clinical studies as well as in post-marketing surveillance. Previous evidence suggested that drug exposure during periods of inflammation could increase an individual's susceptibility to drug hepatoxicity. The antithyroid drugs, methimazole (MMI) and propylthiouracil (PTU) can cause adverse reactions in patients, with liver as a usual target. We tested the hypothesis that MMI and PTU could be rendered hepatotoxic in animals undergoing a modest inflammation. Mice were treated with a nonhepatotoxic dose of LPS (100 µg/kg, i.p) or its vehicle. Nonhepatotoxic doses of MMI (10, 25 and 50 mg/kg, oral) and PTU (10, 25 and 50 mg/kg, oral) were administered two hours after LPS treatment. It was found that liver injury was evident only in animals received both drug and LPS, as estimated by increases in serum alanine aminotransferase (ALT), lactate dehydrogenase (LDH), aspartate aminotransferase (AST), and TNF-α. An increase in liver myeloperoxidase (MPO) enzyme activity and tissue lipid peroxidation (LPO) in addition of liver glutathione (GSH) depletion were also detected in LPS and antithyroid drugs cotreated animals. Furthermore, histopathological changes including, endotheliitis, fatty changes, severe inflammatory cells infiltration (hepatitis) and sinusoidal congestion were detected in liver tissue. Methyl palmitate (2 g/kg, i.v, 44 hours before LPS), as a macrophage suppressor, significantly alleviated antithyroids hepatotoxicity in LPS-treated animals. The results indicate a synergistic liver injury from antithyroid drugs and bacterial lipopolysaccharide coexposure.
药物性肝损伤是临床研究和上市后监测中的一个主要关注点。先前的证据表明,在炎症期间暴露于药物会增加个体对药物肝毒性的易感性。抗甲状腺药物甲巯咪唑(MMI)和丙基硫氧嘧啶(PTU)可引起患者不良反应,肝脏是常见的靶器官。我们检验了这样一个假设,即在经历适度炎症的动物中,MMI 和 PTU 可能会变得具有肝毒性。用小剂量 LPS(100μg/kg,腹腔注射)或其载体处理小鼠。在 LPS 处理后两小时给予非肝毒性剂量的 MMI(10、25 和 50mg/kg,口服)和 PTU(10、25 和 50mg/kg,口服)。结果发现,只有在接受药物和 LPS 治疗的动物中才会出现肝损伤,这可以通过血清丙氨酸氨基转移酶(ALT)、乳酸脱氢酶(LDH)、天冬氨酸氨基转移酶(AST)和 TNF-α的增加来估计。在 LPS 和抗甲状腺药物共同处理的动物中,还检测到肝髓过氧化物酶(MPO)酶活性和组织脂质过氧化(LPO)增加以及肝谷胱甘肽(GSH)耗竭。此外,在肝组织中还检测到包括内皮炎、脂肪变性、严重炎症细胞浸润(肝炎)和窦状隙充血在内的组织学变化。作为巨噬细胞抑制剂的肉豆蔻酸甲酯(2g/kg,静脉注射,在 LPS 前 44 小时),可显著减轻 LPS 处理动物的抗甲状腺药物肝毒性。结果表明,抗甲状腺药物和细菌脂多糖共同暴露会导致协同性肝损伤。