Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway
Background. Hepatic ischemia reperfusion (IR) injury is a common phenomenon in transplantation or trauma. The aim of the present study was to determine the protective effect of quercetin (QE) on hepatic IR injury via the ERK/NF-κB pathway. Methods. Mice were randomized into the sham, IR, QE100 + IR,...
Saved in:
Main Authors: | , , , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2017-01-01
|
Series: | Gastroenterology Research and Practice |
Online Access: | http://dx.doi.org/10.1155/2017/9724217 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832567201235730432 |
---|---|
author | Liwei Wu Qinghui Zhang Weiqi Dai Sainan Li Jiao Feng Jingjing Li Tong Liu Shizan Xu Wenwen Wang Xiya Lu Qiang Yu Kan Chen Yujing Xia Jie Lu Yingqun Zhou Xiaoming Fan Chuanyong Guo |
author_facet | Liwei Wu Qinghui Zhang Weiqi Dai Sainan Li Jiao Feng Jingjing Li Tong Liu Shizan Xu Wenwen Wang Xiya Lu Qiang Yu Kan Chen Yujing Xia Jie Lu Yingqun Zhou Xiaoming Fan Chuanyong Guo |
author_sort | Liwei Wu |
collection | DOAJ |
description | Background. Hepatic ischemia reperfusion (IR) injury is a common phenomenon in transplantation or trauma. The aim of the present study was to determine the protective effect of quercetin (QE) on hepatic IR injury via the ERK/NF-κB pathway. Methods. Mice were randomized into the sham, IR, QE100 + IR, and QE200 + IR groups. Quercetin was administered intragastrically daily at two doses (100 mg/kg and 200 mg/kg) for 5 days prior to IR injury. The expression levels of liver enzymes, inflammatory cytokines, and other marker proteins were determined at 2, 8, and 24 hours after IR. And they were compared among these groups. Results. Compared with the IR group, the treatment of QE reduced the release of cytokines, leading to inhibition of apoptosis and autophagy via downregulation of the ERK/NF-κB pathway in this model of hepatic IR injury. Conclusion. Apoptosis and autophagy caused by hepatic IR injury were inhibited by QE following a reduction in the release of inflammatory cytokines, and the relationship between the two may be associated with inactivation of the ERK/NF-κB pathway. |
format | Article |
id | doaj-art-d51dffd26ee741f79af659e525191e11 |
institution | Kabale University |
issn | 1687-6121 1687-630X |
language | English |
publishDate | 2017-01-01 |
publisher | Wiley |
record_format | Article |
series | Gastroenterology Research and Practice |
spelling | doaj-art-d51dffd26ee741f79af659e525191e112025-02-03T01:02:15ZengWileyGastroenterology Research and Practice1687-61211687-630X2017-01-01201710.1155/2017/97242179724217Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB PathwayLiwei Wu0Qinghui Zhang1Weiqi Dai2Sainan Li3Jiao Feng4Jingjing Li5Tong Liu6Shizan Xu7Wenwen Wang8Xiya Lu9Qiang Yu10Kan Chen11Yujing Xia12Jie Lu13Yingqun Zhou14Xiaoming Fan15Chuanyong Guo16Department of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Clinical Laboratory, Kunshan First People’s Hospital Affiliated to Jiangsu University, Kunshan, Jiangsu 215300, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, School of Clinical Medicine of Nanjing Medical University, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, School of Clinical Medicine of Nanjing Medical University, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Jinshan Hospital of Fudan University, Jinshan, Shanghai 201508, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaBackground. Hepatic ischemia reperfusion (IR) injury is a common phenomenon in transplantation or trauma. The aim of the present study was to determine the protective effect of quercetin (QE) on hepatic IR injury via the ERK/NF-κB pathway. Methods. Mice were randomized into the sham, IR, QE100 + IR, and QE200 + IR groups. Quercetin was administered intragastrically daily at two doses (100 mg/kg and 200 mg/kg) for 5 days prior to IR injury. The expression levels of liver enzymes, inflammatory cytokines, and other marker proteins were determined at 2, 8, and 24 hours after IR. And they were compared among these groups. Results. Compared with the IR group, the treatment of QE reduced the release of cytokines, leading to inhibition of apoptosis and autophagy via downregulation of the ERK/NF-κB pathway in this model of hepatic IR injury. Conclusion. Apoptosis and autophagy caused by hepatic IR injury were inhibited by QE following a reduction in the release of inflammatory cytokines, and the relationship between the two may be associated with inactivation of the ERK/NF-κB pathway.http://dx.doi.org/10.1155/2017/9724217 |
spellingShingle | Liwei Wu Qinghui Zhang Weiqi Dai Sainan Li Jiao Feng Jingjing Li Tong Liu Shizan Xu Wenwen Wang Xiya Lu Qiang Yu Kan Chen Yujing Xia Jie Lu Yingqun Zhou Xiaoming Fan Chuanyong Guo Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway Gastroenterology Research and Practice |
title | Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway |
title_full | Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway |
title_fullStr | Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway |
title_full_unstemmed | Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway |
title_short | Quercetin Pretreatment Attenuates Hepatic Ischemia Reperfusion-Induced Apoptosis and Autophagy by Inhibiting ERK/NF-κB Pathway |
title_sort | quercetin pretreatment attenuates hepatic ischemia reperfusion induced apoptosis and autophagy by inhibiting erk nf κb pathway |
url | http://dx.doi.org/10.1155/2017/9724217 |
work_keys_str_mv | AT liweiwu quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT qinghuizhang quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT weiqidai quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT sainanli quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT jiaofeng quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT jingjingli quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT tongliu quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT shizanxu quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT wenwenwang quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT xiyalu quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT qiangyu quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT kanchen quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT yujingxia quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT jielu quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT yingqunzhou quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT xiaomingfan quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway AT chuanyongguo quercetinpretreatmentattenuateshepaticischemiareperfusioninducedapoptosisandautophagybyinhibitingerknfkbpathway |