Effect of Pu-erh tea on acetaminophen-induced hepatotoxicity assessed by physiological, metabolomic, and transcriptomic analyses

被引:0
作者
Cao, Xinxin [1 ]
Zhang, Kangqing [2 ]
Wang, Xuekai [3 ]
Yao, Fan [1 ]
Sun, Jing [1 ]
Li, Yuanhang [1 ]
Sun, Dandan [1 ,4 ]
Liu, Yujun [1 ]
Sui, Jinling [2 ]
机构
[1] Beijing Forestry Univ, Coll Biol Sci & Biotechnol, Natl Engn Lab Tree Breeding, Beijing 100083, Peoples R China
[2] Beijing Forestry Univ, Sch Ecol & Nat Conservat, Beijing 100083, Peoples R China
[3] China Agr Univ, Coll Grassland Sci & Technol, Beijing 100193, Peoples R China
[4] Shandong Acad Chinese Med, Jinan 250014, Peoples R China
关键词
Pu-erh tea; APAP; Hepatotoxicity; Transcriptomics; Metabolomics; THYROID-HORMONE; GROWTH-FACTOR; LIVER-INJURY; GINSENG; PARAXANTHINE; TOXICITY; CAFFEINE; EXTRACT; CELLS;
D O I
10.1016/j.jff.2022.105059
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Acetaminophen (APAP) is a painkiller that can cause hepatotoxicity if taken in excess. We investigated the effect of pu-erh tea extract (PTE) on hepatotoxicity induced by excess APAP using physiological, metabolomic, and transcriptomic analyses. PTE decreased levels of oxidative stress, inflammatory response, and apoptosis markers induced by excess APAP. And 156 metabolites and 703 genes were identified as differentially expressed metabolites and differentially expressed genes, respectively. KEGG enrichment analysis revealed that PTE and overdose of APAP altered tyrosine, caffeine, and amino acid-related metabolism. Six differentially expressed metabolites associated with these pathways have hepatoprotective effects and were upregulated by PTE pretreatment. The expression levels of 10 vital differentially expressed genes regulating these metabolites were verified by qRT-PCR. The findings confirm the beneficial role of PTE pretreatment in alleviating the hepatotoxicity caused by overdose of APAP, indicating that PTE can be used as an effective dietary supplement for the development of functional foods.
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页数:14
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