Acetaminophen Test Battery (ATB): A Comprehensive Method to Study Acetaminophen-Induced Acute Liver Injury

被引:12
作者
Bhushan, Bharat [1 ,2 ]
Apte, Udayan [3 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA
[2] Univ Pittsburgh, Sch Med, Pittsburgh Liver Res Ctr, Pittsburgh, PA USA
[3] Univ Kansas, Med Ctr, Dept Pharmacol Toxicol & Therapeut, 3901 Rainbow Blvd,MS1018,HLSIC 4087, Kansas City, KS 66103 USA
来源
GENE EXPRESSION-THE JOURNAL OF LIVER RESEARCH | 2020年 / 20卷 / 02期
关键词
Acetaminophen toxicity; Acute liver failure (ALF); Acute liver injury (ALI); Acetaminophen test battery; Liver regeneration;
D O I
10.3727/105221620X15901763757677
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Acetaminophen (APAP) overdose is the major cause of acute liver failure (ALF) in the Western world. Extensive research is ongoing to identify the mechanisms of APAP-induced ALF. APAP-induced acute liver injury is also one of the most commonly studied drug-induced liver injury models in the field of hepatotoxicity. APAP toxicity is triphasic and includes three mechanistically interlinked but temporally distinct phases of initiation, progression, and recovery/regeneration. Despite how commonly it is studied, the methods to study APAP toxicity differ significantly, often leading to confusing and contradictory data. There are number of reviews on mechanisms of APAP toxicity, but a detailed mechanism-based comprehensive method and list of assays that covers all phases of APAP hepatotoxicity are missing. The goal of this review is to provide a standard protocol and guidelines to study APAP toxicity in mice including a "test battery" that can help investigators to comprehensively analyze APAP toxicity in the specific context of their hypothesis. Further, we will identify the major roadblocks and common technical problems that can significantly affect the results. This acetaminophen test battery (ATB) will be an excellent guide for scientists studying this most common and clinically relevant drug-induced liver injury and will also be helpful as a roadmap for hypothesis development to study novel mechanisms.
引用
收藏
页码:125 / 138
页数:14
相关论文
共 82 条
[1]   4-Methylpyrazole protects against acetaminophen hepatotoxicity in mice and in primary human hepatocytes [J].
Akakpo, J. Y. ;
Ramachandran, A. ;
Kandel, S. E. ;
Ni, H. M. ;
Kumer, S. C. ;
Rumack, B. H. ;
Jaeschke, H. .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2018, 37 (12) :1310-1322
[2]   RETRACTED: Molecular forms of HMGB1 and keratin-18 as mechanistic biomarkers for mode of cell death and prognosis during clinical acetaminophen hepatotoxicity (Publication with Expression of Concern. See vol. 73, pg. 1297, 2020) (Publication with Expression of Concern. See vol. 69, pg. 1402, 2018) (Retracted article. See vol. 73, pg. 1297, 2020) [J].
Antoine, Daniel J. ;
Jenkins, Rosalind E. ;
Dear, James W. ;
Williams, Dominic P. ;
McGill, Mitchell R. ;
Sharpe, Matthew R. ;
Craig, Darren G. ;
Simpson, Kenneth J. ;
Jaeschke, Hartmut ;
Park, B. Kevin .
JOURNAL OF HEPATOLOGY, 2012, 56 (05) :1070-1079
[3]   High-Mobility Group Box-1 Protein and Keratin-18, Circulating Serum Proteins Informative of Acetaminophen-Induced Necrosis and Apoptosis In Vivo [J].
Antoine, Daniel J. ;
Williams, Dominic P. ;
Kipar, Anja ;
Jenkins, Rosalind E. ;
Regan, Sophie L. ;
Sathish, Jean G. ;
Kitteringham, Neil R. ;
Park, B. Kevin .
TOXICOLOGICAL SCIENCES, 2009, 112 (02) :521-531
[4]   Source and characterization of hepatic macrophages in acetaminophen-induced acute liver failure in humans [J].
Antoniades, Charalambos Gustav ;
Quaglia, Alberto ;
Taams, Leonie S. ;
Mitry, Ragai R. ;
Hussain, Munther ;
Abeles, Robin ;
Possamai, Lucia A. ;
Bruce, Matthew ;
McPhail, Mark ;
Starling, Christopher ;
Wagner, Bart ;
Barnardo, Adrian ;
Pomplun, Sabine ;
Auzinger, Georg ;
Bernal, William ;
Heaton, Nigel ;
Vergani, Diego ;
Thursz, Mark R. ;
Wendon, Julia .
HEPATOLOGY, 2012, 56 (02) :735-746
[5]   Beta-Catenin Activation Promotes Liver Regeneration after Acetaminophen-Induced Injury [J].
Apte, Udayan ;
Singh, Sucha ;
Zeng, Gang ;
Cieply, Benjamin ;
Virji, Mohamed A. ;
Wu, Tong ;
Monga, Satdarshan P. S. .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 175 (03) :1056-1065
[6]   Mitochondrial Bax translocation accelerates DNA fragmentation and cell necrosis in a murine model of acetaminophen hepatotoxicity [J].
Bajt, Mary Lynn ;
Farhood, Anwar ;
Lemasters, John J. ;
Jaeschke, Hartmut .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 324 (01) :8-14
[7]   Nuclear translocation of endonuclease G and apoptosis-inducing factor during acetaminophen-induced liver cell injury [J].
Bajt, Mary Lynn ;
Cover, Cathleen ;
Lemasters, John J. ;
Jaeschke, Hartmut .
TOXICOLOGICAL SCIENCES, 2006, 94 (01) :217-225
[8]   Apoptosis-Inducing Factor Modulates Mitochondrial Oxidant Stress in Acetaminophen Hepatotoxicity [J].
Bajt, Mary Lynn ;
Ramachandran, Anup ;
Yan, Hui-Min ;
Lebofsky, Margitta ;
Farhood, Anwar ;
Lemasters, John J. ;
Jaeschke, Hartmut .
TOXICOLOGICAL SCIENCES, 2011, 122 (02) :598-605
[9]   Scavenging peroxynitrite with glutathione promotes regeneration and enhances survival during Acetaminophen-induced liver injury in mice [J].
Bajt, ML ;
Knight, TR ;
Farhood, A ;
Jaeschke, H .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 307 (01) :67-73
[10]   Role of epidermal growth factor receptor in liver injury and lipid metabolism: Emerging new roles for an old receptor [J].
Bhushan, Bharat ;
Michalopoulos, George K. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2020, 324