Haasio K, Sopanen L, Vaalavirta L, Lindén I B, Heinonen E H
Orion Corporation, Orion Pharma, Espoo, Finland.
J Neural Transm (Vienna). 2001;108(1):79-91. doi: 10.1007/s007020170099.
Entacapone and tolcapone are novel COMT (catechol-O-methyltransferase) inhibitors indicated for the adjunctive treatment of Parkinson's disease (PD) in combination with levodopa. The marketing authorisation of tolcapone was suspended in the European Union (EU) in 1998 mainly due to severe abnormal hepatic reactions. This fact raised concern about the safety of COMT inhibitors in the treatment of parkinsonian patients. In order to investigate whether these COMT inhibitors exhibit different effects on the liver comparative toxicological studies were performed in the rat. Short term toxicological studies in rats at high oral doses of entacapone and tolcapone (200, 400 or 600mg/kg daily) were carried out. Tolcapone (400 mg/kg/day or 600 mg/kg/day) increased mortality after only one week treatment and induced signs of toxicity such as a rise in body temperature, stimulation of respiration and rapid onset of rigor mortis after death. Entacapone did not show any adverse effects at the tested dose levels. In the histopathological examination liver cell necrosis was observed in the tolcapone (400 and 600mg/kg/day) treated rats, but it revealed no treatment related signs of toxicity in entacapone-treated rats. We conclude that the toxicological profile of the two COMT inhibitors, entacapone and tolcapone, differ from each other, tolcapone--unlike entacapone--showed hepatotoxicity.
恩他卡朋和托卡朋是新型儿茶酚-O-甲基转移酶(COMT)抑制剂,适用于与左旋多巴联合用于帕金森病(PD)的辅助治疗。托卡朋的上市许可于1998年在欧盟被暂停,主要是由于严重的肝脏异常反应。这一事实引发了对COMT抑制剂治疗帕金森病患者安全性的担忧。为了研究这些COMT抑制剂对肝脏是否表现出不同的影响,在大鼠中进行了比较毒理学研究。对大鼠进行了高口服剂量(每日200、400或600mg/kg)的恩他卡朋和托卡朋的短期毒理学研究。托卡朋(400mg/kg/天或600mg/kg/天)仅治疗一周后就增加了死亡率,并诱发了毒性迹象,如体温升高、呼吸刺激和死后迅速出现尸僵。恩他卡朋在测试剂量水平下未显示任何不良反应。在组织病理学检查中,在托卡朋(400和600mg/kg/天)治疗的大鼠中观察到肝细胞坏死,但在恩他卡朋治疗的大鼠中未发现与治疗相关的毒性迹象。我们得出结论,两种COMT抑制剂恩他卡朋和托卡朋的毒理学特征彼此不同,与恩他卡朋不同——托卡朋表现出肝毒性。