Lack of mitochondrial Cyp2E1 drives acetaminophen-induced ER stress-mediated apoptosis in mouse and human kidneys: Inhibition by 4-methylpyrazole but not N-acetylcysteine
Author:
Publisher
Elsevier BV
Subject
Toxicology
Reference77 articles.
1. Desorption electrospray ionization mass spectrometry imaging allows spatial localization of changes in acetaminophen metabolism in the liver after intervention with 4-methylpyrazole;Akakpo;J. Am. Soc. Mass Spectrom.,2022
2. Delayed administration of N-acetylcysteine blunts recovery after an acetaminophen overdose unlike 4-methylpyrazole;Akakpo;Arch. Toxicol.,2021
3. Comparing N-acetylcysteine and 4-methylpyrazole as antidotes for acetaminophen overdose;Akakpo;Arch. Toxicol.,2022
4. Delayed treatment with 4-methylpyrazole protects against acetaminophen hepatotoxicity in mice by inhibition of c-jun n-terminal kinase;Akakpo;Toxicol. Sci.,2019
5. 4-methylpyrazole protects against acetaminophen-induced acute kidney injury;Akakpo;Toxicol. Appl. Pharmacol.,2020
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2. N-acetylcysteine in Kidney Disease: Molecular Mechanisms, Pharmacokinetics, and Clinical Effectiveness;Kidney International Reports;2024-07
3. Clinically relevant therapeutic approaches against acetaminophen hepatotoxicity and acute liver failure;Biochemical Pharmacology;2024-02
4. Spatial analysis of renal acetaminophen metabolism and its modulation by 4-methylpyrazole with DESI mass spectrometry imaging;Toxicological Sciences;2024-01-30
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