Fang Zhi-E, Wang Chunyu, Niu Ming, Liu Tingting, Ren Lutong, Li Qiang, Li Zhiyong, Wei Ziying, Lin Li, Mu Wenqing, Gao Yuan, Xiao Xiaohe, Bai Zhaofang
School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Front Genet. 2022 Mar 25;13:840961. doi: 10.3389/fgene.2022.840961. eCollection 2022.
Aristolochic acid (AA) is a group of structurally related compounds what have been used to treat various diseases in recent decades. Aristolochic acid I (AAI), an important ingredient, has been associated with tumorigenesis. Recently, some studies indicated that AAI could induce liver injury in mice of different age, but comprehensive mechanisms of AAI-induced differences in liver injury in various age groups have not yet been elucidated. This study aims to evaluate the causal relationship between AAI-induced liver injury and age based on neonatal mice and adult mice. A survival experiment indicated that all neonatal mice survived. Moreover, the adult mice in the high-dose AAI group all died, whereas half of the adult mice in the low-dose AAI group died. In observation experiments, AAI induced more severe liver injury in neonatal mice than adult mice under long-term than short-term exposure. Furthermore, integrated metabolomics and transcriptomics indicated that AAI disturbing steroid hormone biosynthesis, arachidonic acid metabolism, the drug metabolism-cytochrome P450 pathway and glycerophospholipid metabolism induced neonatal mice liver injury. The important role of age in AAI-induced liver injury was illustrated in our study. This study also lays a solid foundation for scientific supervision of AA safety.
马兜铃酸(AA)是一组结构相关的化合物,近几十年来一直被用于治疗各种疾病。马兜铃酸I(AAI)作为一种重要成分,与肿瘤发生有关。最近,一些研究表明,AAI可在不同年龄的小鼠中诱导肝损伤,但AAI在不同年龄组中诱导肝损伤差异的综合机制尚未阐明。本研究旨在基于新生小鼠和成年小鼠评估AAI诱导的肝损伤与年龄之间的因果关系。一项生存实验表明,所有新生小鼠均存活。此外,高剂量AAI组的成年小鼠全部死亡,而低剂量AAI组的成年小鼠有一半死亡。在观察实验中,长期暴露下,AAI在新生小鼠中比在成年小鼠中诱导更严重的肝损伤。此外,综合代谢组学和转录组学表明,AAI干扰类固醇激素生物合成、花生四烯酸代谢、药物代谢-细胞色素P450途径和甘油磷脂代谢,从而诱导新生小鼠肝损伤。我们的研究阐明了年龄在AAI诱导肝损伤中的重要作用。本研究也为马兜铃酸安全性的科学监管奠定了坚实基础。