Literature DB >> 29682868

Role and mechanisms of autophagy in acetaminophen-induced liver injury.

Xiaojuan Chao1, Hua Wang1,2, Hartmut Jaeschke1, Wen-Xing Ding1.   

Abstract

Acetaminophen (APAP) overdose is the most frequent cause of acute liver failure in the USA and many other countries. Although the metabolism and pathogenesis of APAP has been extensively investigated for decades, the mechanisms by which APAP induces liver injury are incompletely known, which hampers the development of effective therapeutic approaches to tackle this important clinical problem. Autophagy is a highly conserved intracellular degradation pathway, which aims at recycling cellular components and damaged organelles in response to adverse environmental conditions and stresses as a survival mechanism. There is accumulating evidence indicating that autophagy is activated in response to APAP overdose in specific liver zone areas, and pharmacological activation of autophagy protects against APAP-induced liver injury. Increasing evidence also suggests that hepatic autophagy is impaired in nonalcoholic fatty livers (NAFLD), and NAFLD patients are more susceptible to APAP-induced liver injury. Here, we summarized the current progress on the role and mechanisms of autophagy in protecting against APAP-induced liver injury.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  acetaminophen; acetaminophen protein adducts; autophagy; liver injury; mitophagy

Mesh:

Substances:

Year:  2018        PMID: 29682868      PMCID: PMC6105454          DOI: 10.1111/liv.13866

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  130 in total

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2.  A role for mitochondria in NLRP3 inflammasome activation.

Authors:  Rongbin Zhou; Amir S Yazdi; Philippe Menu; Jürg Tschopp
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3.  Loss of autophagy promotes murine acetaminophen hepatotoxicity.

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Journal:  Nature       Date:  2014-06-04       Impact factor: 49.962

5.  Syndecan-1 limits the progression of liver injury and promotes liver repair in acetaminophen-induced liver injury in mice.

Authors:  Eon Jeong Nam; Kazutaka Hayashida; Rafael S Aquino; John R Couchman; Rosemary A Kozar; Jian Liu; Pyong Woo Park
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6.  Broad activation of the ubiquitin-proteasome system by Parkin is critical for mitophagy.

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Review 7.  Nonalcoholic fatty liver disease.

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  33 in total

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Review 3.  Acetaminophen Toxicity: A History of Serendipity and Unintended Consequences.

Authors:  William M Lee
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Review 4.  Emerging and established modes of cell death during acetaminophen-induced liver injury.

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5.  Delayed Treatment With 4-Methylpyrazole Protects Against Acetaminophen Hepatotoxicity in Mice by Inhibition of c-Jun n-Terminal Kinase.

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Review 6.  Mitochondrial stress response in drug-induced liver injury.

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7.  Goji Ferment Ameliorated Acetaminophen-Induced Liver Injury in vitro and in vivo.

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Journal:  Exp Ther Med       Date:  2021-05-03       Impact factor: 2.447

Review 10.  Novel strategies for the treatment of acetaminophen hepatotoxicity.

Authors:  Jephte Y Akakpo; Anup Ramachandran; Hartmut Jaeschke
Journal:  Expert Opin Drug Metab Toxicol       Date:  2020-09-14       Impact factor: 4.481

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