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Protective role of c-Jun N-terminal kinase-2 (JNK2) in ibuprofen-induced acute liver injury
被引:12
|作者:
Zoubek, Miguel E.
[1
,2
]
Woitok, Marius M.
[1
]
Sydor, Svenja
[3
,4
]
Nelson, Leonard J.
[5
]
Bechmann, Lars P.
[3
,4
]
Lucena, Maria I.
[6
]
Andrade, Raul J.
[6
]
Bast, Aalt
[2
]
Koek, Ger H.
[7
,8
,9
]
Trautwein, Christian
[1
]
Cubero, Francisco J.
[1
,10
,11
]
机构:
[1] Univ Hosp RWTH Aachen, Dept Internal Med 3, Pauwelsstr 30, D-52074 Aachen, Germany
[2] Maastricht Univ, Dept Toxicol, Fac Hlth Med & Life Sci, Sch Nutr Toxicol & Metab NUTRIM, Maastricht, Netherlands
[3] Univ Hosp Duisburg Essen, Dept Gastroenterol & Hepatol, Essen, Germany
[4] Otto von Guericke Univ, Dept Gastroenterol Hepatol & Infect Dis, Magdeburg, Germany
[5] Univ Edinburgh, Human Tissue Engn, Inst Bioengn IBioE, Faraday Bldg, Edinburgh, Midlothian, Scotland
[6] Univ Malaga, Inst Invest Biomed Malaga IBIMA, Hosp Univ Virgen de la Victoria, Unidad Gest Clin Enfermedades Digest,CIBERehd,Ser, Malaga, Spain
[7] Maastricht Univ, Div Gastroenterol & Hepatol, Med Ctr, Dept Internal Med, Maastricht, Netherlands
[8] Maastricht Univ, Sch Nutr & Translat Res Metab NUTRIM, Maastricht, Netherlands
[9] Univ Hosp RWTH Aachen, Dept Visceral Surg & Transplantat, Aachen, Germany
[10] Univ Complutense Madrid, Sch Med, Dept Immunol Ophthalmol & ORL, Madrid 28040, Spain
[11] 12 Octubre Hlth Res Inst Imas12, Madrid, Spain
来源:
关键词:
ibuprofen;
toxicity;
drug-induced liver injury (DILI);
JNK;
liver failure;
VANISHING BILE-DUCT;
STEVENS-JOHNSON-SYNDROME;
HEPATITIS;
HEPATOTOXICITY;
RESPIRATION;
POPULATION;
TOXICITY;
MEDIATOR;
NECROSIS;
OUTCOMES;
D O I:
10.1002/path.5174
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Ibuprofen is a worldwide used non-steroidal anti-inflammatory drug which may cause acute liver injury (ALI) requiring liver transplantation. We aimed to unveil the molecular pathways involved in triggering ibuprofen-induced ALI, which, at present, remain elusive. First, we investigated activation of essential pathways in human liver sections of ibuprofen-induced ALI. Next, we assessed the cytotoxicity of ibuprofen in vitro and developed a novel murine model of ibuprofen intoxication. To assess the role of JNK, we used animals carrying constitutive deletion of c-Jun N-terminal kinase 1 (Jnk1(-/-)) or Jnk2 (Jnk2(-/-)) expression and included investigations using animals with hepatocyte-specific Jnk deletion either genetically (Jnk1(Delta hepa)) or by siRNA (siJnk2(Delta hepa)). We found in human and murine samples of ibuprofen-induced acute liver failure that JNK phosphorylation was increased in the cytoplasm of hepatocytes and other non-liver parenchymal cells (non-LPCs) compared with healthy tissue. In mice, ibuprofen intoxication resulted in a significantly stronger degree of liver injury compared with vehicle-treated controls as evidenced by serum transaminases, and hepatic histopathology. Next, we investigated molecular pathways. PKC alpha, AKT, JNK and RIPK1 were significantly increased 8 h after ibuprofen intoxication. Constitutive Jnk1(-/-) and Jnk2(-/-) deficient mice exhibited increased liver dysfunction compared to wild-type (WT) animals. Furthermore, siJnk2(Delta hepa) animals showed a dramatic increase in biochemical markers of liver function, which correlated with significantly higher serum liver enzymes and worsened liver histology, and MAPK activation compared to Jnk1(Delta hepa) or WT animals. In our study, cytoplasmic JNK activation in hepatocytes and other non-LPCs is a hallmark of human and murine ibuprofen-induced ALI. Functional in vivo analysis demonstrated a protective role of hepatocyte-specific Jnk2 during ibuprofen ALI. Copyright (c) 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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页码:110 / 122
页数:13
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