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...

Full description

Saved in:
Bibliographic Details
Published inAsian Pacific journal of tropical medicine Vol. 9; no. 3; pp. 283 - 287
Main Authors He, Ping, Zeng, Bo, Zhang, Xiao-Li, Fang, Dian-Liang, Zhou, Xia-Qia, Wan, Ke-Qiang, Tian, Wen-Guang
Format Journal Article
LanguageEnglish
Published India Elsevier B.V 01.03.2016
Subjects
Online AccessGet full text

Cover

Loading…
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.
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
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26972403$$D View this record in MEDLINE/PubMed
BookMark eNqNkUtv1TAQhS1URC-lvwAJeckmwY_YuV6wQBUvqRIsYIksX2dymZDYwXYq9d_jcgsLFoA3ntF8Z0Y65zE5CzEAIU85aznj-sXUunUqSytq0zLeMmEekJ2QSjQd7_QZ2XFjVNPrTp2Ty5wnVp8UxvTyETkX2vSiY3JHvnxMsYAveAMUxrFWNI7UrXEtMWOmGY_BzU2C4za7guFIv2FwGSinGL7iAUtM1B0dhlzogh7oXFelOpy2dPuEPBzdnOHy_r8gn9-8_nT1rrn-8Pb91avrxnd8bxpjmBHOOSMHNwBjWkjpTOdhMAfBBjUozXoxdHu519xowWXXeyXZwblacikvyPPT3jXF7xvkYhfMHubZBYhbtryvF5Q0Qv8H2stO7JVWFX12j26HBQa7JlxcurW_3KuAPAE-xZwTjL8RzuxdTHayP2OydzFZxm2NqarMHyqPpXobQ0kO539oX560UN28QUg2e4RQncJUs7NDxL_qfwDyka2o
CitedBy_id crossref_primary_10_1016_j_ejmech_2023_115889
crossref_primary_10_1097_TP_0000000000002466
crossref_primary_10_1111_jgh_16087
crossref_primary_10_1007_s00109_020_01878_y
crossref_primary_10_3389_fphys_2021_669331
crossref_primary_10_1042_BST20160473
crossref_primary_10_1080_14789450_2019_1676735
crossref_primary_10_1016_j_ygeno_2024_110983
crossref_primary_10_1097_st9_0000000000000056
crossref_primary_10_3389_fphar_2022_917162
crossref_primary_10_3389_fmicb_2022_847653
crossref_primary_10_1016_j_bbagen_2016_09_028
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
ContentType Journal Article
Copyright 2016 Hainan Medical College
Copyright © 2016 Hainan Medical College. Production and hosting by Elsevier B.V. All rights reserved.
Copyright_xml – notice: 2016 Hainan Medical College
– notice: Copyright © 2016 Hainan Medical College. Production and hosting by Elsevier B.V. All rights reserved.
DBID 6I.
AAFTH
AAYXX
CITATION
NPM
7X8
7T2
C1K
F1W
H95
H97
L.G
DOI 10.1016/j.apjtm.2016.01.029
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
PubMed
MEDLINE - Academic
Health and Safety Science Abstracts (Full archive)
Environmental Sciences and Pollution Management
ASFA: Aquatic Sciences and Fisheries Abstracts
Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources
Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality
Aquatic Science & Fisheries Abstracts (ASFA) Professional
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
Aquatic Science & Fisheries Abstracts (ASFA) Professional
Health & Safety Science Abstracts
Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources
Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality
ASFA: Aquatic Sciences and Fisheries Abstracts
Environmental Sciences and Pollution Management
DatabaseTitleList
MEDLINE - Academic
PubMed
Aquatic Science & Fisheries Abstracts (ASFA) Professional
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2352-4146
EndPage 287
ExternalDocumentID 26972403
10_1016_j_apjtm_2016_01_029
S1995764516000304
Genre Journal Article
GrantInformation_xml – fundername: Soft Science Foundation
  grantid: 2011BE5015
GroupedDBID ---
--K
-05
-0E
-SE
-S~
.~1
0R~
0SF
188
1B1
1~.
1~5
2B.
2C~
4.4
457
4G.
53G
5VR
5VS
6I.
7-5
71M
92F
92I
92M
93N
93R
9D9
9DE
AACTN
AAEDW
AAFTH
AAIKJ
AALRI
AAQFI
AAXUO
ABBQC
ABJNI
ABKZE
ABMAC
ACGFS
ADEZE
AEKER
AENEX
AEXQZ
AFUIB
AGHFR
AGYEJ
AITUG
AJRQY
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
CAJEE
CAJUS
CCEZO
CHBEP
CIEJG
DYU
EBS
ECGQY
EJD
EP3
FA0
FDB
FEDTE
FNPLU
GBLVA
GROUPED_DOAJ
HVGLF
HZ~
J1W
JUIAU
KQ8
M41
MO0
M~E
N9A
NCXOZ
O-L
O9-
OK1
OVD
OZF
P-8
P-9
PC.
Q--
Q-4
Q38
R-E
RIG
RMW
ROL
RT5
S..
SDF
SES
SSZ
T8U
TCJ
TEORI
TGQ
U1F
U1G
U5E
U5O
UZ5
W3E
WFFXF
~MZ
AAYWO
AAYXX
ABWVN
ACRPL
ACVFH
ADCNI
ADJBI
ADNMO
ADVLN
AEUPX
AFPUW
AIGII
AKBMS
AKRWK
AKYEP
CITATION
H13
NPM
7X8
7T2
C1K
F1W
H95
H97
L.G
ID FETCH-LOGICAL-c4189-99092aaa93dade006233a94ced9b20d5d56072d4838619621347c530baa134133
IEDL.DBID .~1
ISSN 1995-7645
IngestDate Fri Jul 11 09:39:02 EDT 2025
Thu Jul 10 22:37:08 EDT 2025
Fri Jan 03 00:55:36 EST 2025
Tue Jul 01 03:00:03 EDT 2025
Thu Apr 24 22:50:07 EDT 2025
Fri Feb 23 02:13:02 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Apoptosis signal-regulating kinase 1
Acetaminophen
JNK
Liver injury
Language English
License http://creativecommons.org/licenses/by-nc-nd/4.0
http://www.elsevier.com/tdm/userlicense/1.0
Copyright © 2016 Hainan Medical College. Production and hosting by Elsevier B.V. All rights reserved.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4189-99092aaa93dade006233a94ced9b20d5d56072d4838619621347c530baa134133
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.sciencedirect.com/science/article/pii/S1995764516000304
PMID 26972403
PQID 1773428565
PQPubID 23479
PageCount 5
ParticipantIDs proquest_miscellaneous_1790953926
proquest_miscellaneous_1773428565
pubmed_primary_26972403
crossref_primary_10_1016_j_apjtm_2016_01_029
crossref_citationtrail_10_1016_j_apjtm_2016_01_029
elsevier_sciencedirect_doi_10_1016_j_apjtm_2016_01_029
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate March 2016
2016-03-00
2016-Mar
20160301
PublicationDateYYYYMMDD 2016-03-01
PublicationDate_xml – month: 03
  year: 2016
  text: March 2016
PublicationDecade 2010
PublicationPlace India
PublicationPlace_xml – name: India
PublicationTitle Asian Pacific journal of tropical medicine
PublicationTitleAlternate Asian Pac J Trop Med
PublicationYear 2016
Publisher Elsevier B.V
Publisher_xml – name: Elsevier B.V
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
SSID ssj0000329973
Score 2.1277018
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...
SourceID proquest
pubmed
crossref
elsevier
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 283
SubjectTerms Acetaminophen
Apoptosis signal-regulating kinase 1
JNK
Liver injury
Title Protective effect of apoptosis signal-regulating kinase 1 inhibitor against mice liver injury
URI https://dx.doi.org/10.1016/j.apjtm.2016.01.029
https://www.ncbi.nlm.nih.gov/pubmed/26972403
https://www.proquest.com/docview/1773428565
https://www.proquest.com/docview/1790953926
Volume 9
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LS8QwEA7iQbyIb9cXETxat23SZHMUdVkERdAFPUhIm652Xdqyu1797c4k7YIH9-Cl0DaBMEnmm0lmviHknPPYAtCkAYCDCvhIZIGxWRLEiQ1VKkaJcFn89w9iMOR3L8nLCrluc2EwrLLR_V6nO23dfOk20uzWRdF9wuRiKbDQrDPskROUc4mr_PI7WpyzhAwUrrtodsnI2KElH3JhXqYezzEjPRKevlP9BVB_GaAOiPqbZKOxIOmVH-QWWcnLbbJ239yR75C3R0-9AGqM-mgNWo2oqat6Xs2KGcWIDTMJpr4IPSAX_SxKwDIa0aL8KFLY4lNq3k0BhiPFYvV0grEb8HMM8t8lw_7t8_UgaIooBBmPeioAtFGxMUYxa2yOKZOMGcVBvCqNQ5tYMHlkbHmP9cCXEkjwJrOEhakxyPXG2B5ZLasyPyBUIR28AX8xFzn4OaHKQitVbySSFFRmLjskbiWns4ZhHAtdTHQbSjbWTtwaxa3DSIO4O-Ri0an2BBvLm4t2SvSvdaIBApZ3PGsnUMMOwmsRU-bV10xHUjJwwsCyXdZGITGfikWH7PvZX4w2Fkoiq-Hhf4d2RNbxzUe2HZPV-fQrPwFTZ56eurUMz5vX4Q9lAvqs
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fT9swED4Bk4CXifFj69iGkXgkNIkdp36cEKjbKEICJF6Q5cQpS1clUVte-du5s5NKPNCHvca2ZN3Z993Fd98BnAgRWwSaLEBwUIEYyzwwNk-COLGhyuQ4ka6Kf3Qth_fi90PysAbnXS0MpVW2tt_bdGet2y_9Vpr9piz7t1RcnEpqNOsce7EOHwReX2pjcPYSLX-0hBwtrntpdtXItKJjH3J5XqaZLKgkPZKev1O9h1DveaAOiS534GPrQrKffpefYK2odmFz1D6S78HjjedeQDvGfLoGq8fMNHWzqOflnFHKhpkGM9-FHqGL_SsrBDMWsbL6W2Z4x2fMPJkSPUdG3erZlJI3cHCCCtiH-8uLu_Nh0HZRCHIRDVSAcKNiY4zi1tiCaiY5N0qgfFUWhzax6POksRUDPsBgShLDW5onPMyMIbI3zg9go6qr4gswRXzwBgPGQhYY6IQqD22qBmOZZGgzi7QHcSc5nbcU49TpYqq7XLKJduLWJG4dRhrF3YPT5aLGM2ysni47leg3B0UjBqxeeNwpUOMVoncRUxX181xHacoxCkPXdtUcRcx8KpY9-Oy1v9xtLFVKtIZf_3drR7A1vBtd6atf138OYZtGfJrbN9hYzJ6L7-j3LLIf7ly_AhCW_LU
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Protective+effect+of+apoptosis+signal-regulating+kinase+1+inhibitor+against+mice+liver+injury&rft.jtitle=Asian+Pacific+journal+of+tropical+medicine&rft.au=He%2C+Ping&rft.au=Zeng%2C+Bo&rft.au=Zhang%2C+Xiao-Li&rft.au=Fang%2C+Dian-Liang&rft.date=2016-03-01&rft.pub=Elsevier+B.V&rft.issn=1995-7645&rft.eissn=2352-4146&rft.volume=9&rft.issue=3&rft.spage=283&rft.epage=287&rft_id=info:doi/10.1016%2Fj.apjtm.2016.01.029&rft.externalDocID=S1995764516000304
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1995-7645&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1995-7645&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1995-7645&client=summon