The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation
Triptolide (TP), an active ingredient of Tripterygium wilfordii Hook f., possesses a wide range of biological activities. Oxidative stress likely plays a role in TP-induced hepatotoxicity. Isoliquiritigenin (ISL) and glycyrrhetinic acid (GA) are potent hepatoprotection agents. The aim of the present...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2016-01-01
|
Series: | Evidence-Based Complementary and Alternative Medicine |
Online Access: | http://dx.doi.org/10.1155/2016/8912184 |
id |
doaj-c5f9c98a96bb47af9c02787dbbadaccc |
---|---|
record_format |
Article |
spelling |
doaj-c5f9c98a96bb47af9c02787dbbadaccc2020-11-24T20:48:21ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882016-01-01201610.1155/2016/89121848912184The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 ActivationLing-Juan Cao0Huan-De Li1Miao Yan2Zhi-Hua Li3Hui Gong4Pei Jiang5Yang Deng6Ping-Fei Fang7Bi-Kui Zhang8Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, ChinaTriptolide (TP), an active ingredient of Tripterygium wilfordii Hook f., possesses a wide range of biological activities. Oxidative stress likely plays a role in TP-induced hepatotoxicity. Isoliquiritigenin (ISL) and glycyrrhetinic acid (GA) are potent hepatoprotection agents. The aim of the present study was to investigate whether Nrf2 pathway is associated with the protective effects of ISL and GA against TP-induced oxidative stress or not. HepG2 cells were treated with TP (50 nM) for 24 h after pretreatment with ISL and GA (5, 10, and 20 μM) for 12 h and 24 h, respectively. The results demonstrated that TP treatment significantly increased ROS levels and decreased GSH levels. Both ISL and GA pretreatment decreased ROS and meanwhile enhanced intracellular GSH content. Additionally, TP treatment obviously decreased the protein expression of Nrf2 and its target genes including HO-1 and MRP2 except NQO1. Moreover, both ISL and GA displayed activities as inducers of Nrf2 and increased the expression of HO-1, NQO1, and MRP2. Taken together the current data confirmed that ISL and GA could activate the Nrf2 antioxidant response in HepG2 cells, increasing the expression of its target genes which may be partly associated with their protective effects in TP-induced oxidative stress.http://dx.doi.org/10.1155/2016/8912184 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ling-Juan Cao Huan-De Li Miao Yan Zhi-Hua Li Hui Gong Pei Jiang Yang Deng Ping-Fei Fang Bi-Kui Zhang |
spellingShingle |
Ling-Juan Cao Huan-De Li Miao Yan Zhi-Hua Li Hui Gong Pei Jiang Yang Deng Ping-Fei Fang Bi-Kui Zhang The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation Evidence-Based Complementary and Alternative Medicine |
author_facet |
Ling-Juan Cao Huan-De Li Miao Yan Zhi-Hua Li Hui Gong Pei Jiang Yang Deng Ping-Fei Fang Bi-Kui Zhang |
author_sort |
Ling-Juan Cao |
title |
The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation |
title_short |
The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation |
title_full |
The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation |
title_fullStr |
The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation |
title_full_unstemmed |
The Protective Effects of Isoliquiritigenin and Glycyrrhetinic Acid against Triptolide-Induced Oxidative Stress in HepG2 Cells Involve Nrf2 Activation |
title_sort |
protective effects of isoliquiritigenin and glycyrrhetinic acid against triptolide-induced oxidative stress in hepg2 cells involve nrf2 activation |
publisher |
Hindawi Limited |
series |
Evidence-Based Complementary and Alternative Medicine |
issn |
1741-427X 1741-4288 |
publishDate |
2016-01-01 |
description |
Triptolide (TP), an active ingredient of Tripterygium wilfordii Hook f., possesses a wide range of biological activities. Oxidative stress likely plays a role in TP-induced hepatotoxicity. Isoliquiritigenin (ISL) and glycyrrhetinic acid (GA) are potent hepatoprotection agents. The aim of the present study was to investigate whether Nrf2 pathway is associated with the protective effects of ISL and GA against TP-induced oxidative stress or not. HepG2 cells were treated with TP (50 nM) for 24 h after pretreatment with ISL and GA (5, 10, and 20 μM) for 12 h and 24 h, respectively. The results demonstrated that TP treatment significantly increased ROS levels and decreased GSH levels. Both ISL and GA pretreatment decreased ROS and meanwhile enhanced intracellular GSH content. Additionally, TP treatment obviously decreased the protein expression of Nrf2 and its target genes including HO-1 and MRP2 except NQO1. Moreover, both ISL and GA displayed activities as inducers of Nrf2 and increased the expression of HO-1, NQO1, and MRP2. Taken together the current data confirmed that ISL and GA could activate the Nrf2 antioxidant response in HepG2 cells, increasing the expression of its target genes which may be partly associated with their protective effects in TP-induced oxidative stress. |
url |
http://dx.doi.org/10.1155/2016/8912184 |
work_keys_str_mv |
AT lingjuancao theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT huandeli theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT miaoyan theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT zhihuali theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT huigong theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT peijiang theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT yangdeng theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT pingfeifang theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT bikuizhang theprotectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT lingjuancao protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT huandeli protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT miaoyan protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT zhihuali protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT huigong protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT peijiang protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT yangdeng protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT pingfeifang protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation AT bikuizhang protectiveeffectsofisoliquiritigeninandglycyrrhetinicacidagainsttriptolideinducedoxidativestressinhepg2cellsinvolvenrf2activation |
_version_ |
1716808078992605184 |