Fibroblast growth factor 21 protects against acetaminophen-induced hepatotoxicity by potentiating peroxisome proliferator-activated receptor coactivator protein-1α-mediated antioxidant capacity in mice

Author:

Ye Dewei123,Wang Yudong12,Li Huating4,Jia Weiping4,Man Kwan5,Lo Chung Mau5,Wang Yu13,Lam Karen S.L.12,Xu Aimin123

Affiliation:

1. State Key Laboratory of Pharmaceutical Biotechnology; University of Hong Kong; Hong Kong China

2. Department of Medicine; University of Hong Kong; Hong Kong China

3. Department of Pharmacology & Pharmacy; University of Hong Kong; Hong Kong China

4. Department of Endocrinology and Metabolism; Shanghai Jiao Tong University Affiliated Sixth People's Hospital; Shanghai China

5. Department of Surgery; University of Hong Kong; Hong Kong China

Funder

Research Grant Council of Hong Kong

Publisher

Wiley

Subject

Hepatology

Reference38 articles.

1. Acute liver failure;Bernal;Lancet,2010

2. Current issues with acetaminophen hepatotoxicity-a clinically relevant model to test the efficacy of natural products;Jaeschke;Life Sci,2011

3. Subcellular binding and effects on calcium homeostasis produced by acetaminophen and a nonhepatotoxic regioisomer, 3′-hydroxyacetanilide, in mouse-liver;Tirmenstein;J Biol Chem,1989

4. The mechanism underlying acetaminophen-induced hepatotoxicity in humans and mice involves mitochondrial damage and nuclear DNA fragmentation;McGill;J Clin Invest,2012

5. Acetaminophen hepatotoxicity and repair: the role of sterile inflammation and innate immunity;Jaeschke;Liver Int,2012

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