1. Academic Validation
  2. Integration of Transcriptomic and Metabolomic Data to Compare the Hepatotoxicity of Neonatal and Adult Mice Exposed to Aristolochic Acid I

Integration of Transcriptomic and Metabolomic Data to Compare the Hepatotoxicity of Neonatal and Adult Mice Exposed to Aristolochic Acid I

  • Front Genet. 2022 Mar 25;13:840961. doi: 10.3389/fgene.2022.840961.
Zhi-E Fang 1 2 3 Chunyu Wang 2 3 Ming Niu 2 3 Tingting Liu 2 3 Lutong Ren 2 3 Qiang Li 2 3 Zhiyong Li 2 3 Ziying Wei 2 3 Li Lin 2 3 Wenqing Mu 2 3 Yuan Gao 4 Xiaohe Xiao 1 2 3 Zhaofang Bai 2 3
Affiliations

Affiliations

  • 1 School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
  • 2 Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
  • 3 China Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
  • 4 School of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Abstract

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.

Keywords

adult; aristolochic acid I; liver injury; metabolomics; neonatal; transcriptomics.

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