Protective effect of apoptosis signal-regulating kinase 1 inhibitor against mice liver injury
To explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on acetaminophen-induced liver injury in mice. The model of liver injury was established by administration of acetaminophen (APAP) (300 mg/kg, i.p.) on C57BL/6 mice. Fort...
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Published in | Asian Pacific journal of tropical medicine Vol. 9; no. 3; pp. 283 - 287 |
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Language | English |
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01.03.2016
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Abstract | To explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on acetaminophen-induced liver injury in mice.
The model of liver injury was established by administration of acetaminophen (APAP) (300 mg/kg, i.p.) on C57BL/6 mice. Forty-eight male C57BL/6 mice were randomly divided into four groups, consisting of control group, GS group (GS-459679, 30 mg/kg, i.p.), APAP-induced group, and GS combined with APAP-induced group. For GS combined with APAP-induced group, mice were treated with GS 30 min prior to administration of APAP. After mice were euthanized at 6 h or 12 h, respectively, serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed, and mRNA levels of TNF-α, IL-6 and IL-1β were tested. The activity of glutathione (GSH), oxidized GSH (GSSG) and malondialdehyde were quantified. In addition, ASK1, P-ASK1, JNK and P-JNK protein levels were tested in all groups.
The ASK1 and P-ASK1 levels were up-regulated in APAP-induced group. Compared to the control group, serum levels of ALT and AST, and mRNA levels of TNF-α, IL-6 and IL-1β were increased in APAP-induced group. Meanwhile, the levels of MAD and GSSG, and the ratio of GSSG/GSH were higher and the JNK was activatedin APAP-induced group compared with that in control group. However, compared to APAP-induced group, GS combined with APAP-induced group displayed a decrease of protein expression levels of ASK1, P-ASK1 and P-JNK, a reduction of serum levels of ALT and AST, a decrease in TNF-α, IL-6 and IL-1β mRNA levels, and a low ration of GSSG/GSH.
GS-459679 treatment effectively down-regulates ASK1 and P-ASK1 expression. Addition of GS-459679 decreases the generation of liver metabolites and inflammatory factors, reduces oxidative stress reaction, inhibits JNK activation, and then protects the responsiveness to APAP-induced liver injury. |
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AbstractList | To explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on acetaminophen-induced liver injury in mice.
The model of liver injury was established by administration of acetaminophen (APAP) (300 mg/kg, i.p.) on C57BL/6 mice. Forty-eight male C57BL/6 mice were randomly divided into four groups, consisting of control group, GS group (GS-459679, 30 mg/kg, i.p.), APAP-induced group, and GS combined with APAP-induced group. For GS combined with APAP-induced group, mice were treated with GS 30 min prior to administration of APAP. After mice were euthanized at 6 h or 12 h, respectively, serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed, and mRNA levels of TNF-α, IL-6 and IL-1β were tested. The activity of glutathione (GSH), oxidized GSH (GSSG) and malondialdehyde were quantified. In addition, ASK1, P-ASK1, JNK and P-JNK protein levels were tested in all groups.
The ASK1 and P-ASK1 levels were up-regulated in APAP-induced group. Compared to the control group, serum levels of ALT and AST, and mRNA levels of TNF-α, IL-6 and IL-1β were increased in APAP-induced group. Meanwhile, the levels of MAD and GSSG, and the ratio of GSSG/GSH were higher and the JNK was activatedin APAP-induced group compared with that in control group. However, compared to APAP-induced group, GS combined with APAP-induced group displayed a decrease of protein expression levels of ASK1, P-ASK1 and P-JNK, a reduction of serum levels of ALT and AST, a decrease in TNF-α, IL-6 and IL-1β mRNA levels, and a low ration of GSSG/GSH.
GS-459679 treatment effectively down-regulates ASK1 and P-ASK1 expression. Addition of GS-459679 decreases the generation of liver metabolites and inflammatory factors, reduces oxidative stress reaction, inhibits JNK activation, and then protects the responsiveness to APAP-induced liver injury. OBJECTIVETo explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on acetaminophen-induced liver injury in mice.METHODSThe model of liver injury was established by administration of acetaminophen (APAP) (300 mg/kg, i.p.) on C57BL/6 mice. Forty-eight male C57BL/6 mice were randomly divided into four groups, consisting of control group, GS group (GS-459679, 30 mg/kg, i.p.), APAP-induced group, and GS combined with APAP-induced group. For GS combined with APAP-induced group, mice were treated with GS 30 min prior to administration of APAP. After mice were euthanized at 6 h or 12 h, respectively, serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed, and mRNA levels of TNF-α, IL-6 and IL-1β were tested. The activity of glutathione (GSH), oxidized GSH (GSSG) and malondialdehyde were quantified. In addition, ASK1, P-ASK1, JNK and P-JNK protein levels were tested in all groups.RESULTSThe ASK1 and P-ASK1 levels were up-regulated in APAP-induced group. Compared to the control group, serum levels of ALT and AST, and mRNA levels of TNF-α, IL-6 and IL-1β were increased in APAP-induced group. Meanwhile, the levels of MAD and GSSG, and the ratio of GSSG/GSH were higher and the JNK was activatedin APAP-induced group compared with that in control group. However, compared to APAP-induced group, GS combined with APAP-induced group displayed a decrease of protein expression levels of ASK1, P-ASK1 and P-JNK, a reduction of serum levels of ALT and AST, a decrease in TNF-α, IL-6 and IL-1β mRNA levels, and a low ration of GSSG/GSH.CONCLUSIONSGS-459679 treatment effectively down-regulates ASK1 and P-ASK1 expression. Addition of GS-459679 decreases the generation of liver metabolites and inflammatory factors, reduces oxidative stress reaction, inhibits JNK activation, and then protects the responsiveness to APAP-induced liver injury. Objective: To explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on acetaminophen-induced liver injury in mice. Methods: The model of liver injury was established by administration of acetaminophen (APAP) (300 mg/kg, i.p.) on C57BL/6 mice. Forty-eight male C57BL/6 mice were randomly divided into four groups, consisting of control group, GS group (GS-459679, 30 mg/kg, i.p.), APAP-induced group, and GS combined with APAP-induced group. For GS combined with APAP-induced group, mice were treated with GS 30 min prior to administration of APAP. After mice were euthanized at 6 h or 12 h, respectively, serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed, and mRNA levels of TNF- alpha , IL-6 and IL-1 beta were tested. The activity of glutathione (GSH), oxidized GSH (GSSG) and malondialdehyde were quantified. In addition, ASK1, P-ASK1, JNK and P-JNK protein levels were tested in all groups. Results: The ASK1 and P-ASK1 levels were up-regulated in APAP-induced group. Compared to the control group, serum levels of ALT and AST, and mRNA levels of TNF- alpha , IL-6 and IL-1 beta were increased in APAP-induced group. Meanwhile, the levels of MAD and GSSG, and the ratio of GSSG/GSH were higher and the JNK was activatedin APAP-induced group compared with that in control group. However, compared to APAP-induced group, GS combined with APAP-induced group displayed a decrease of protein expression levels of ASK1, P-ASK1 and P-JNK, a reduction of serum levels of ALT and AST, a decrease in TNF- alpha , IL-6 and IL-1 beta mRNA levels, and a low ration of GSSG/GSH. Conclusions: GS-459679 treatment effectively down-regulates ASK1 and P-ASK1 expression. Addition of GS-459679 decreases the generation of liver metabolites and inflammatory factors, reduces oxidative stress reaction, inhibits JNK activation, and then protects the responsiveness to APAP-induced liver injury. |
Author | Wan, Ke-Qiang Zeng, Bo Zhang, Xiao-Li Tian, Wen-Guang Zhou, Xia-Qia He, Ping Fang, Dian-Liang |
Author_xml | – sequence: 1 givenname: Ping surname: He fullname: He, Ping organization: Department of Gastroenterology, Yongchuan Hospital of Chongqing Medical University, Chongqing, China – sequence: 2 givenname: Bo surname: Zeng fullname: Zeng, Bo organization: Department of Gastroenterology, Yongchuan Hospital of Chongqing Medical University, Chongqing, China – sequence: 3 givenname: Xiao-Li surname: Zhang fullname: Zhang, Xiao-Li organization: Department of Gastroenterology, Yongchuan Hospital of Chongqing Medical University, Chongqing, China – sequence: 4 givenname: Dian-Liang surname: Fang fullname: Fang, Dian-Liang organization: Department of Gastroenterology, Yongchuan Hospital of Chongqing Medical University, Chongqing, China – sequence: 5 givenname: Xia-Qia surname: Zhou fullname: Zhou, Xia-Qia organization: Department of Infectious Diseases, Yongchuan Hospital of Chongqing Medical University, Chongqing, China – sequence: 6 givenname: Ke-Qiang surname: Wan fullname: Wan, Ke-Qiang organization: Department of Infectious Diseases, Yongchuan Hospital of Chongqing Medical University, Chongqing, China – sequence: 7 givenname: Wen-Guang surname: Tian fullname: Tian, Wen-Guang email: twg9366@163.com organization: Department of Infectious Diseases, Yongchuan Hospital of Chongqing Medical University, Chongqing, China |
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Cites_doi | 10.1097/MOG.0b013e3283528b5d 10.1038/nrgastro.2011.22 10.1016/j.taap.2015.03.019 10.3109/03602532.2011.602688 10.1016/j.cld.2013.07.002 10.1111/j.1440-1746.2010.06592.x 10.1074/jbc.M114.623280 10.1111/cas.12024 10.1016/j.taap.2010.04.015 10.1016/j.taap.2014.05.010 10.3390/ijms150915754 10.1053/j.gastro.2008.07.006 10.1016/j.tips.2013.01.009 10.1002/jcb.22384 10.1016/j.freeradbiomed.2010.02.024 10.1016/j.taap.2012.08.015 10.1093/toxsci/kfs283 10.1007/s00011-013-0671-7 10.1074/jbc.M111.225946 |
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Keywords | Apoptosis signal-regulating kinase 1 Acetaminophen JNK Liver injury |
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References | Lilly (bib3) 2012 Yu, Richardson (bib16) 2011; 286 Hyun, Hur, Mun, Kim, Woo (bib19) 2010; 109 Yuan, Kaplowitz (bib4) 2013; 17 Nakagawa, Maeda, Hikiba, Ohmae, Shibata, Yanai (bib9) 2008; 135 Xie, Ramachandran, Breckenridge, Liles, Lebofsky, Farhood (bib14) 2015; 286 Pires, Marques, Pereira, David, Gomides, Dias (bib20) 2014; 63 Jaeschke (bib10) 2011; 26 Han, Dara, Win, Than, Yuan, Abbasi (bib6) 2013; 34 Mcgill, Williams, Xie, Ramachandran, Jaeschke (bib17) 2012; 264 Watanabe, Sekine, Naguro, Sekine, Ichijo (bib15) 2015; 290 Niso-Santano, González-Polo, Bravo-San Pedro, Gómez-Sánchez, Lastres-Becker, Ortiz-Ortiz (bib13) 2010; 48 Xie, Mcgill, Dorko, Kumer, Schmitt, Forster (bib7) 2014; 279 Jaeschke, Mcgill, Ramachandran (bib8) 2012; 44 Grant, Rockey (bib1) 2012; 28 Hayakawa, Hirata, Sakitani, Nakagawa, Nakata, Kinoshita (bib12) 2012; 103 Xie, Williams, Mcgill, Lebofsky, Ramachandran, Jaeschke (bib18) 2013; 131 Saito, Lemasters, Jaeschke (bib5) 2010; 246 Liang, Zhang, Xue, Zhao, Zhang, Pei (bib11) 2014; 15 Tujios, Fontana (bib2) 2011; 8 Liang (10.1016/j.apjtm.2016.01.029_bib11) 2014; 15 Saito (10.1016/j.apjtm.2016.01.029_bib5) 2010; 246 Pires (10.1016/j.apjtm.2016.01.029_bib20) 2014; 63 Hayakawa (10.1016/j.apjtm.2016.01.029_bib12) 2012; 103 Hyun (10.1016/j.apjtm.2016.01.029_bib19) 2010; 109 Jaeschke (10.1016/j.apjtm.2016.01.029_bib10) 2011; 26 Xie (10.1016/j.apjtm.2016.01.029_bib7) 2014; 279 Jaeschke (10.1016/j.apjtm.2016.01.029_bib8) 2012; 44 Nakagawa (10.1016/j.apjtm.2016.01.029_bib9) 2008; 135 Tujios (10.1016/j.apjtm.2016.01.029_bib2) 2011; 8 Grant (10.1016/j.apjtm.2016.01.029_bib1) 2012; 28 Niso-Santano (10.1016/j.apjtm.2016.01.029_bib13) 2010; 48 Lilly (10.1016/j.apjtm.2016.01.029_bib3) 2012 Xie (10.1016/j.apjtm.2016.01.029_bib18) 2013; 131 Mcgill (10.1016/j.apjtm.2016.01.029_bib17) 2012; 264 Yuan (10.1016/j.apjtm.2016.01.029_bib4) 2013; 17 Watanabe (10.1016/j.apjtm.2016.01.029_bib15) 2015; 290 Yu (10.1016/j.apjtm.2016.01.029_bib16) 2011; 286 Han (10.1016/j.apjtm.2016.01.029_bib6) 2013; 34 Xie (10.1016/j.apjtm.2016.01.029_bib14) 2015; 286 |
References_xml | – volume: 279 start-page: 266 year: 2014 end-page: 274 ident: bib7 article-title: Mechanisms of acetaminophen-induced cell death in primary human hepatocytes publication-title: Toxicol Appl Pharmacol – volume: 131 start-page: 325 year: 2013 end-page: 335 ident: bib18 article-title: Purinergic receptor antagonist A438079 protects against acetaminophen-induced liver injury by inhibiting p450 isoenzymes, not by inflammasome activation publication-title: Toxicol Sci – volume: 17 start-page: 507 year: 2013 end-page: 518 ident: bib4 article-title: Mechanisms of drug-induced liver injury publication-title: Clin Liver Dis – volume: 34 start-page: 243 year: 2013 end-page: 253 ident: bib6 article-title: Regulation of drug-induced liver injury by signal transduction pathways: critical role of mitochondria publication-title: Trends Pharmacol Sci – volume: 109 start-page: 329 year: 2010 end-page: 338 ident: bib19 article-title: BBR induces apoptosis in HepG2 cell through an Akt-ASK1-ROS-p38MAPKs-linked cascade publication-title: J Cell Biochem – volume: 26 start-page: 173 year: 2011 end-page: 179 ident: bib10 article-title: Reactive oxygen and mechanisms of inflammatory liver injury: present concepts publication-title: J Gastroenterol Hepatol – volume: 246 start-page: 8 year: 2010 end-page: 17 ident: bib5 article-title: c-Jun N-terminal kinase modulates oxidant stress and peroxynitrite formation independent of inducible nitric oxide synthase in acetaminophen hepatotoxicity publication-title: Toxicol Appl Pharmacol – volume: 48 start-page: 1370 year: 2010 end-page: 1381 ident: bib13 article-title: Activation of apoptosis signal-regulating kinase 1 is a key factor in paraquat-induced cell death: modulation by the Nrf2/Trx axis publication-title: Free Radic Biol Med – volume: 63 start-page: 61 year: 2014 end-page: 69 ident: bib20 article-title: Interleukin-4 deficiency protects mice from acetaminophen-induced liver injury and inflammation by prevention of glutathione depletion publication-title: Inflamm Res – volume: 44 start-page: 88 year: 2012 end-page: 106 ident: bib8 article-title: Oxidant stress, mitochondria, and cell death mechanisms in drug-induced liver injury: lessons learned from acetaminophen hepatotoxicity publication-title: Drug Metab Rev – volume: 286 start-page: 15413 year: 2011 end-page: 15427 ident: bib16 article-title: Cellular iron depletion stimulates the JNK and p38 MAPK signaling transduction pathways, dissociation of ASK1-thioredoxin, and activation of ASK1 publication-title: J Biol Chem – volume: 8 start-page: 202 year: 2011 end-page: 211 ident: bib2 article-title: Mechanisms of drug-induced liver injury: from bedside to bench publication-title: Nat Rev Gastroenterol Hepatol – volume: 103 start-page: 2181 year: 2012 end-page: 2185 ident: bib12 article-title: Apoptosis signal-regulating kinase-1 inhibitor as a potent therapeutic drug for the treatment of gastric cancer publication-title: Cancer Sci – volume: 286 start-page: 1 year: 2015 end-page: 9 ident: bib14 article-title: Inhibitor of apoptosis signal-regulating kinase 1 protects against acetaminophen-induced liver injury publication-title: Toxicol Appl Pharmacol – start-page: 235 year: 2012 end-page: 243 ident: bib3 article-title: Drug-induced liver disease publication-title: Hepatol diagnosis and clinical management – volume: 15 start-page: 15754 year: 2014 end-page: 15765 ident: bib11 article-title: Curcumin induced human gastric cancer BGC-823 cells apoptosis by ROS-mediated ASK1-MKK4-JNK stress signaling pathway publication-title: Int JMol Sci – volume: 28 start-page: 198 year: 2012 end-page: 202 ident: bib1 article-title: Drug-induced liver injury publication-title: Curr Opin Gastroenterol – volume: 264 start-page: 387 year: 2012 end-page: 394 ident: bib17 article-title: Acetaminophen-induced liver injury in rats and mice: comparison of protein adducts, mitochondrial dysfunction, and oxidative stress in the mechanism of toxicity publication-title: Toxicol Appl Pharmacol – volume: 290 start-page: 10791 year: 2015 end-page: 10803 ident: bib15 article-title: Apoptosis signal-regulating kinase 1 (ASK1)-p38 pathway-dependent cytoplasmic translocation of the orphan nuclear receptor NR4A2 is required for oxidative stress-induced necrosis publication-title: J Biol Chem – volume: 135 start-page: 1311 year: 2008 end-page: 1321 ident: bib9 article-title: Deletion of apoptosis signal-regulating kinase 1 attenuates acetaminophen-induced liver injury by inhibiting c-Jun N-terminal kinase activation publication-title: Gastroenterology – volume: 28 start-page: 198 issue: 3 year: 2012 ident: 10.1016/j.apjtm.2016.01.029_bib1 article-title: Drug-induced liver injury publication-title: Curr Opin Gastroenterol doi: 10.1097/MOG.0b013e3283528b5d – volume: 8 start-page: 202 issue: 4 year: 2011 ident: 10.1016/j.apjtm.2016.01.029_bib2 article-title: Mechanisms of drug-induced liver injury: from bedside to bench publication-title: Nat Rev Gastroenterol Hepatol doi: 10.1038/nrgastro.2011.22 – volume: 286 start-page: 1 issue: 1 year: 2015 ident: 10.1016/j.apjtm.2016.01.029_bib14 article-title: Inhibitor of apoptosis signal-regulating kinase 1 protects against acetaminophen-induced liver injury publication-title: Toxicol Appl Pharmacol doi: 10.1016/j.taap.2015.03.019 – volume: 44 start-page: 88 issue: 1 year: 2012 ident: 10.1016/j.apjtm.2016.01.029_bib8 article-title: Oxidant stress, mitochondria, and cell death mechanisms in drug-induced liver injury: lessons learned from acetaminophen hepatotoxicity publication-title: Drug Metab Rev doi: 10.3109/03602532.2011.602688 – volume: 17 start-page: 507 issue: 4 year: 2013 ident: 10.1016/j.apjtm.2016.01.029_bib4 article-title: Mechanisms of drug-induced liver injury publication-title: Clin Liver Dis doi: 10.1016/j.cld.2013.07.002 – volume: 26 start-page: 173 issue: Suppl. 1 year: 2011 ident: 10.1016/j.apjtm.2016.01.029_bib10 article-title: Reactive oxygen and mechanisms of inflammatory liver injury: present concepts publication-title: J Gastroenterol Hepatol doi: 10.1111/j.1440-1746.2010.06592.x – volume: 290 start-page: 10791 issue: 17 year: 2015 ident: 10.1016/j.apjtm.2016.01.029_bib15 article-title: Apoptosis signal-regulating kinase 1 (ASK1)-p38 pathway-dependent cytoplasmic translocation of the orphan nuclear receptor NR4A2 is required for oxidative stress-induced necrosis publication-title: J Biol Chem doi: 10.1074/jbc.M114.623280 – volume: 103 start-page: 2181 issue: 12 year: 2012 ident: 10.1016/j.apjtm.2016.01.029_bib12 article-title: Apoptosis signal-regulating kinase-1 inhibitor as a potent therapeutic drug for the treatment of gastric cancer publication-title: Cancer Sci doi: 10.1111/cas.12024 – volume: 246 start-page: 8 issue: 1–2 year: 2010 ident: 10.1016/j.apjtm.2016.01.029_bib5 article-title: c-Jun N-terminal kinase modulates oxidant stress and peroxynitrite formation independent of inducible nitric oxide synthase in acetaminophen hepatotoxicity publication-title: Toxicol Appl Pharmacol doi: 10.1016/j.taap.2010.04.015 – volume: 279 start-page: 266 issue: 3 year: 2014 ident: 10.1016/j.apjtm.2016.01.029_bib7 article-title: Mechanisms of acetaminophen-induced cell death in primary human hepatocytes publication-title: Toxicol Appl Pharmacol doi: 10.1016/j.taap.2014.05.010 – volume: 15 start-page: 15754 issue: 9 year: 2014 ident: 10.1016/j.apjtm.2016.01.029_bib11 article-title: Curcumin induced human gastric cancer BGC-823 cells apoptosis by ROS-mediated ASK1-MKK4-JNK stress signaling pathway publication-title: Int JMol Sci doi: 10.3390/ijms150915754 – start-page: 235 year: 2012 ident: 10.1016/j.apjtm.2016.01.029_bib3 article-title: Drug-induced liver disease – volume: 135 start-page: 1311 issue: 4 year: 2008 ident: 10.1016/j.apjtm.2016.01.029_bib9 article-title: Deletion of apoptosis signal-regulating kinase 1 attenuates acetaminophen-induced liver injury by inhibiting c-Jun N-terminal kinase activation publication-title: Gastroenterology doi: 10.1053/j.gastro.2008.07.006 – volume: 34 start-page: 243 issue: 4 year: 2013 ident: 10.1016/j.apjtm.2016.01.029_bib6 article-title: Regulation of drug-induced liver injury by signal transduction pathways: critical role of mitochondria publication-title: Trends Pharmacol Sci doi: 10.1016/j.tips.2013.01.009 – volume: 109 start-page: 329 issue: 2 year: 2010 ident: 10.1016/j.apjtm.2016.01.029_bib19 article-title: BBR induces apoptosis in HepG2 cell through an Akt-ASK1-ROS-p38MAPKs-linked cascade publication-title: J Cell Biochem doi: 10.1002/jcb.22384 – volume: 48 start-page: 1370 issue: 10 year: 2010 ident: 10.1016/j.apjtm.2016.01.029_bib13 article-title: Activation of apoptosis signal-regulating kinase 1 is a key factor in paraquat-induced cell death: modulation by the Nrf2/Trx axis publication-title: Free Radic Biol Med doi: 10.1016/j.freeradbiomed.2010.02.024 – volume: 264 start-page: 387 issue: 3 year: 2012 ident: 10.1016/j.apjtm.2016.01.029_bib17 article-title: Acetaminophen-induced liver injury in rats and mice: comparison of protein adducts, mitochondrial dysfunction, and oxidative stress in the mechanism of toxicity publication-title: Toxicol Appl Pharmacol doi: 10.1016/j.taap.2012.08.015 – volume: 131 start-page: 325 issue: 1 year: 2013 ident: 10.1016/j.apjtm.2016.01.029_bib18 article-title: Purinergic receptor antagonist A438079 protects against acetaminophen-induced liver injury by inhibiting p450 isoenzymes, not by inflammasome activation publication-title: Toxicol Sci doi: 10.1093/toxsci/kfs283 – volume: 63 start-page: 61 issue: 1 year: 2014 ident: 10.1016/j.apjtm.2016.01.029_bib20 article-title: Interleukin-4 deficiency protects mice from acetaminophen-induced liver injury and inflammation by prevention of glutathione depletion publication-title: Inflamm Res doi: 10.1007/s00011-013-0671-7 – volume: 286 start-page: 15413 issue: 17 year: 2011 ident: 10.1016/j.apjtm.2016.01.029_bib16 article-title: Cellular iron depletion stimulates the JNK and p38 MAPK signaling transduction pathways, dissociation of ASK1-thioredoxin, and activation of ASK1 publication-title: J Biol Chem doi: 10.1074/jbc.M111.225946 |
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Snippet | To explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on acetaminophen-induced... OBJECTIVETo explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on... Objective: To explore the protective effect and its molecular mechanism of apoptosis signal-regulating kinase 1 (ASK1) inhibitor (GS-459679) on... |
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SubjectTerms | Acetaminophen Apoptosis signal-regulating kinase 1 JNK Liver injury |
Title | Protective effect of apoptosis signal-regulating kinase 1 inhibitor against mice liver injury |
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