Malak A. Jaber
Potential biomarkers and metabolomics of acetaminophen-induced liver injury during alcohol consumption: A preclinical investigation on C57/BL6 mice
Jaber, Malak A.; Ghanim, Bayan Y.; Al-Natour, Mohammad; Arqoub, Duaa Abu; Abdallah, Qasem; Abdelrazig, Salah; Alkrad, Jamal Alyousse; Kim, Dong-Hyun; Qinna, Nidal A.
Authors
Bayan Y. Ghanim
Mohammad Al-Natour
Duaa Abu Arqoub
Qasem Abdallah
Salah Abdelrazig
Jamal Alyousse Alkrad
Dr DONG-HYUN KIM Dong-hyun.Kim@nottingham.ac.uk
ASSOCIATE PROFESSOR
Nidal A. Qinna
Abstract
The toxic effects of alcohol consumption on population health are significant worldwide and the synergistic toxic effects of concurrent intake of Acetaminophen and alcohol is of clinical concern. The understanding of molecular mechanisms beneath such synergism and acute toxicity may be enhanced through assessing underlying metabolomics changes. The molecular toxic activities of the model hereby, is assessed though metabolomics profile with a view to identifying metabolomics targets which could aid in the management of drug-alcohol interactions. In vivo exposure of C57/BL6 mice to APAP (70 mg/kg), single dose of ethanol (6 g/kg of 40%) and APAP after alcohol consumption was employed. Plasma samples were prepared and subjected to biphasic extraction for complete LC-MS profiling, and tandem mass MS analysis. Among the detected ions, 174 ions had significant (VIP scores >1 and FDR <0.05) changes between groups and were selected as potential biomarkers and significant variables. The presented metabolomics approach highlighted several affected metabolic pathways, including nucleotide and amino acid metabolism; aminoacyl-tRNA biosynthesis as well as bioenergetics of TCA and Krebs cycle. The impact of APAP on the concurrent administration of alcohol showed great biological interactions in the vital ATP and amino acid producing processes. The metabolomics changes show distinct metabolites which are altered to alcohol-APAP consumption while presenting several unneglectable risks on the vitality of metabolites and cellular molecules which shall be concerned. [Abstract copyright: Copyright © 2023 Elsevier Inc. All rights reserved.]
Citation
Jaber, M. A., Ghanim, B. Y., Al-Natour, M., Arqoub, D. A., Abdallah, Q., Abdelrazig, S., Alkrad, J. A., Kim, D.-H., & Qinna, N. A. (2023). Potential biomarkers and metabolomics of acetaminophen-induced liver injury during alcohol consumption: A preclinical investigation on C57/BL6 mice. Toxicology and Applied Pharmacology, 465, Article 116451. https://doi.org/10.1016/j.taap.2023.116451
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 2, 2023 |
Online Publication Date | Mar 10, 2023 |
Publication Date | Apr 15, 2023 |
Deposit Date | Apr 16, 2023 |
Journal | Toxicology and Applied Pharmacology |
Electronic ISSN | 1096-0333 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 465 |
Article Number | 116451 |
DOI | https://doi.org/10.1016/j.taap.2023.116451 |
Keywords | Krebs Cycle, Oxidative Stress, Metabolism, TCA Cycle, Non-targeted LC-MS Metabolomics |
Public URL | https://nottingham-repository.worktribe.com/output/18993206 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S0041008X23000893?via%3Dihub |
Additional Information | This article is maintained by: Elsevier; Article Title: Potential biomarkers and metabolomics of acetaminophen-induced liver injury during alcohol consumption: A preclinical investigation on C57/BL6 mice; Journal Title: Toxicology and Applied Pharmacology; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.taap.2023.116451; Content Type: article; Copyright: © 2023 Elsevier Inc. All rights reserved. |
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