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

被引:11
作者
Fang, Zhi-e [1 ,2 ,3 ]
Wang, Chunyu [2 ,3 ]
Niu, Ming [2 ,3 ]
Liu, Tingting [2 ,3 ]
Ren, Lutong [2 ,3 ]
Li, Qiang [2 ,3 ]
Li, Zhiyong [2 ,3 ]
Wei, Ziying [2 ,3 ]
Lin, Li [2 ,3 ]
Mu, Wenqing [2 ,3 ]
Gao, Yuan [4 ]
Xiao, Xiaohe [1 ,2 ,3 ]
Bai, Zhaofang [2 ,3 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Hepatol, Beijing, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, China Mil Inst Chinese Mat, Med Ctr 5, Beijing, Peoples R China
[4] Capital Med Univ, Sch Tradit Chinese Med, Beijing, Peoples R China
关键词
aristolochic acid I; liver injury; neonatal; adult; metabolomics; transcriptomics; TUMOR INHIBITORS; CYTOCHROMES P450; DNA-ADDUCTS; INDUCTION; ANALOGS; ENZYMES; RAT;
D O I
10.3389/fgene.2022.840961
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页数:12
相关论文
共 44 条
[1]   Aristolochic Acid-Induced Nephrotoxicity: Molecular Mechanisms and Potential Protective Approaches [J].
Anger, Etienne Empweb ;
Yu, Feng ;
Li, Ji .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (03)
[2]   Impact of genetic modulation of SULT1A enzymes on DNA adduct formation by aristolochic acids and 3-nitrobenzanthrone [J].
Arlt, Volker M. ;
Meinl, Walter ;
Florian, Simone ;
Nagy, Eszter ;
Barta, Frantisek ;
Thomann, Marlies ;
Mrizova, Iveta ;
Krais, Annette M. ;
Liu, Maggie ;
Richards, Meirion ;
Mirza, Amin ;
Kopka, Klaus ;
Phillips, David H. ;
Glatt, Hansruedi ;
Stiborova, Marie ;
Schmeiser, Heinz H. .
ARCHIVES OF TOXICOLOGY, 2017, 91 (04) :1957-1975
[3]   Transcriptomic and metabolomic data integration [J].
Cavill, Rachel ;
Jennen, Danyel ;
Kleinjans, Jos ;
Briede, Jacob Jan .
BRIEFINGS IN BIOINFORMATICS, 2016, 17 (05) :891-901
[4]   Herbal Medicine Containing Aristolochic Acid and the Risk of Primary Liver Cancer in Patients with Hepatitis C Virus Infection [J].
Chen, Chi-Jen ;
Yang, Yao-Hsu ;
Lin, Meng-Hung ;
Lee, Chuan-Pin ;
Tsan, Yu-Tse ;
Lai, Ming-Nan ;
Yang, Hsiao-Yu ;
Doyle, Pat ;
Ho, Wen-Chao ;
Chen, Pau-Chung .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2019, 28 (11) :1876-1883
[5]   Herbal medicine containing aristolochic acid and the risk of hepatocellular carcinoma in patients with hepatitis B virus infection [J].
Chen, Chi-Jen ;
Yang, Yao-Hsu ;
Lin, Meng-Hung ;
Lee, Chuan-Pin ;
Tsan, Yu-Tse ;
Lai, Ming-Nan ;
Yang, Hsiao-Yu ;
Ho, Wen-Chao ;
Chen, Pau-Chung .
INTERNATIONAL JOURNAL OF CANCER, 2018, 143 (07) :1578-1587
[6]   8 years post-marketing surveillance between Asari Radix and hepatocellular carcinoma: Nationwide population-based evidence against an association [J].
Chen, Chin-Nu ;
Tsai, Yueh-Ting ;
Lai, Jung-Nien .
JOURNAL OF ETHNOPHARMACOLOGY, 2019, 243
[7]  
Dawson W.R., 1927, PHARM J PHARMACIST, V396, P427
[8]   Induction of cytochromes P450 1A1 and 1A2 suppresses formation of DNA adducts by carcinogenic aristolochic acid I in rats in vivo [J].
Dracinska, Helena ;
Barta, Frantisek ;
Levova, Katerina ;
Hudecova, Alena ;
Moserova, Michaela ;
Schmeiser, Heinz H. ;
Kopka, Klaus ;
Frei, Eva ;
Arlt, Volker M. ;
Stiborova, Marie .
TOXICOLOGY, 2016, 344 :7-18
[9]  
FILITIS L N, 1961, Vopr Onkol, V7(8), P97
[10]   Metabolic activation capacity of neonatal mice in relation to the neonatal mouse tumorigenicity bioassay [J].
Fu, PP ;
Von Tungelin, LS ;
Hammons, GJ ;
McMahon, G ;
Wogan, G ;
Flammang, TJ ;
Kadlubar, FF .
DRUG METABOLISM REVIEWS, 2000, 32 (02) :241-266