Effect of Pu-erh tea on acetaminophen-induced hepatotoxicity assessed by physiological, metabolomic, and transcriptomic analyses. (May 2022)
- Record Type:
- Journal Article
- Title:
- Effect of Pu-erh tea on acetaminophen-induced hepatotoxicity assessed by physiological, metabolomic, and transcriptomic analyses. (May 2022)
- Main Title:
- Effect of Pu-erh tea on acetaminophen-induced hepatotoxicity assessed by physiological, metabolomic, and transcriptomic analyses
- Authors:
- Cao, Xinxin
Zhang, Kangqing
Wang, Xuekai
Yao, Fan
Sun, Jing
Li, Yuanhang
Sun, Dandan
Liu, Yujun
Sui, Jinling - Abstract:
- Graphical abstract: Highlights: PTE pretreatment ameliorated oxidative stress, inflammatory response, and apoptosis of mice caused by excess APAP. PTE pretreatment and APAP overdose altered the metabolic profile and gene expression of liver tissues. PTE induced tyrosine and caffeine metabolism, and alleviated hepatotoxicity induced by excess APAP. Six DEMs and 10 DEGs were biomarkers and key genes for liver protection in high dose APAP exposure. Abstract: 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 beGraphical abstract: Highlights: PTE pretreatment ameliorated oxidative stress, inflammatory response, and apoptosis of mice caused by excess APAP. PTE pretreatment and APAP overdose altered the metabolic profile and gene expression of liver tissues. PTE induced tyrosine and caffeine metabolism, and alleviated hepatotoxicity induced by excess APAP. Six DEMs and 10 DEGs were biomarkers and key genes for liver protection in high dose APAP exposure. Abstract: 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. … (more)
- Is Part Of:
- Journal of functional foods. Volume 92(2022)
- Journal:
- Journal of functional foods
- Issue:
- Volume 92(2022)
- Issue Display:
- Volume 92, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 92
- Issue:
- 2022
- Issue Sort Value:
- 2022-0092-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-05
- Subjects:
- Pu-erh tea -- APAP -- Hepatotoxicity -- Transcriptomics -- Metabolomics
Functional foods -- Analysis -- Periodicals
Food -- Biotechnology -- Periodicals
Nutrition -- Periodicals
613.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/17564646 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jff.2022.105059 ↗
- Languages:
- English
- ISSNs:
- 1756-4646
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4986.807000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21642.xml