Extract of Rhus verniciflua stokes protects against renal ischemia-reperfusion injury by enhancing Nrf2-mediated induction of antioxidant enzymes

被引:13
|
作者
Choi, Du Ri [1 ]
Jeong, Ji Heun [1 ]
Yu, Kwang-Sik [1 ]
Lee, Nam-Seob [1 ]
Jeong, Young-Gil [1 ]
Kim, Do Kyung [1 ]
Na, Chun Soo [2 ]
Na, Dae Seung [2 ]
Hwang, Won Min [3 ]
Han, Seung-Yun [1 ,4 ]
机构
[1] Konyang Univ, Dept Anat, Coll Med, 158 Gwanjeo Dong Ro, Daejeon 302718, South Korea
[2] Lifetree Biotech Co Ltd, Lifetree Biotechnol Inst, Suwon 441813, South Korea
[3] Konyang Univ Hosp, Div Nephrol, Dept Internal Med, 158 Gwanjeo Dong Ro, Daejeon 302718, South Korea
[4] Konyang Univ, Myunggok Res Inst, Coll Med, Daejeon 302718, South Korea
关键词
ischemia-reperfusion injury; acute kidney disease; Rhus verniciflua Stokes; nuclear factor erythroid 2-related factor 2; NRF2/HO-1 SIGNALING PATHWAY; TERT-BUTYL HYDROPEROXIDE; OXIDATIVE STRESS; NRF2-ARE PATHWAY; GALLIC ACID; INFLAMMATION; ACTIVATION; INHIBITION; EXPRESSION; DAMAGE;
D O I
10.3892/etm.2018.5913
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ischemia-reperfusion injury (IRI) may cause acute kidney disease (AKD) by mediating the oxidative stress-induced apoptosis of parenchymal cells. The extract of Rhus verniciflua Stokes (RVS) is used as a traditional herbal medicine as it exhibits anti-oxidant, anti-apoptotic and anti-inflammatory properties. Therefore, the current study investigated the therapeutic effect and the underlying mechanism of RVS on IRI-induced AKD in vivo and in vitro. The current study assessed the effects of RVS on a mouse model of renal IRI and in hypoxic human renal tubular epithelial HK-2 cells. The results demonstrated that the IRI-induced elevation of blood urea nitrogen, serum creatinine and lactate dehydrogenase was significantly attenuated by the intraoral administration of RVS (20 mg/kg/day) for 14 days prior to surgery. It was demonstrated that IRI surgery induced histological damage and cellular apoptosis in renal parenchyma, which were attenuated by pretreatment with RVS. Furthermore, in HK-2 cells incubated with 300 mu M CoCl2 to induce chemical hypoxia, it was demonstrated that RVS treatment significantly inhibited cell death and the production of reactive oxygen species (ROS). Furthermore, RVS treatment upregulated the levels of endogenous antioxidant enzymes, including heme oxygenase-1 and catalase, as well as their upstream regulator nuclear factor erythroid 2-related factor 2, in HK-2 cells. Taken together, these results suggested that the intraoral administration of RVS induces a therapeutic effect on IRI-induced AKD. These effects are at least partly due to the attenuation of ROS production via upregulation of the antioxidant defense system in renal tubular cells.
引用
收藏
页码:3827 / 3835
页数:9
相关论文
共 50 条
  • [31] Knockout of the interleukin-36 receptor protects against renal ischemia-reperfusion injury by reduction of proinflammatory cytokines
    Nishikawa, Hirofumi
    Taniguchi, Yoshinori
    Matsumoto, Tatsuki
    Arima, Naoki
    Masaki, Mamoru
    Shimamura, Yoshiko
    Inoue, Kosuke
    Horino, Taro
    Fujimoto, Shimpei
    Ohko, Kentaro
    Komatsu, Toshihiro
    Udaka, Keiko
    Sano, Shigetoshi
    Terada, Yoshio
    KIDNEY INTERNATIONAL, 2018, 93 (03) : 599 - 614
  • [32] Oridonin Protects against Myocardial Ischemia-Reperfusion Injury by Inhibiting GSDMD-Mediated Pyroptosis
    Lin, Jiahui
    Lai, Xianhui
    Fan, Xiaoxi
    Ye, Bozhi
    Zhong, Lingfeng
    Zhang, Yucong
    Shao, Ruiyin
    Shi, Si
    Huang, Weijian
    Su, Lan
    Ying, Miaomiao
    GENES, 2022, 13 (11)
  • [33] Schizandrin A protects against cerebral ischemia-reperfusion injury by suppressing inflammation and oxidative stress and regulating the AMPK/Nrf2 pathway regulation
    Zhou, Feng
    Wang, Maode
    Ju, Jing
    Wang, Yuan
    Liu, Zhibin
    Zhao, Xiaoping
    Yan, Yongmei
    Yan, Shuguang
    Luo, Xiaozhong
    Fang, Yongjun
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2019, 11 (01): : 199 - 209
  • [34] Growth arrest-specific protein 6 protects against renal ischemia-reperfusion injury
    Giangola, Matthew D.
    Yang, Weng-Lang
    Rajayer, Salil R.
    Kuncewitch, Michael
    Molmenti, Ernesto
    Nicastro, Jeffrey
    Coppa, Gene F.
    Wang, Ping
    JOURNAL OF SURGICAL RESEARCH, 2015, 199 (02) : 572 - 579
  • [35] Hydroxysafflor yellow A protects rat brains against ischemia-reperfusion injury by antioxidant action
    Wei, XB
    Liu, HQ
    Sun, X
    Fu, FH
    Zhang, XM
    Wang, J
    An, J
    Ding, H
    NEUROSCIENCE LETTERS, 2005, 386 (01) : 58 - 62
  • [36] Carbon Monoxide Protects Against Ischemia-reperfusion Injury in Vitro via Antioxidant Properties
    Berne, Jean-Pierre
    Lauzier, Benjamin
    Rochette, Luc
    Vergely, Catherine
    CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2012, 29 (3-4) : 475 - 484
  • [37] Carnosic acid protects against acetaminophen-induced hepatotoxicity by potentiating Nrf2-mediated antioxidant capacity in mice
    Guo, Qi
    Shen, Zhiyang
    Yu, Hongxia
    Lu, Gaofeng
    Yu, Yong
    Liu, Xia
    Zheng, Pengyuan
    KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, 2016, 20 (01) : 15 - 23
  • [38] Salvianolic Acid A Protects Against Oxidative Stress and Apoptosis Induced by Intestinal Ischemia-Reperfusion Injury Through Activation of Nrf2/HO-1 Pathways
    Zu, Guo
    Zhou, Tingting
    Che, Ningwei
    Zhang, Xiangwen
    CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2018, 49 (06) : 2320 - 2332
  • [39] 4-Hydroxy-2-nonenal protects against cardiac ischemia-reperfusion injury via the Nrf2-dependent pathway
    Zhang, Yan
    Sano, Motoaki
    Shinmura, Ken
    Tamaki, Kayoko
    Katsumata, Yoshinori
    Matsuhashi, Tomohiro
    Morizane, Shintaro
    Ito, Hideyuki
    Hishiki, Takako
    Endo, Jin
    Zhou, Heping
    Yuasa, Shinsuke
    Kaneda, Ruri
    Suematsu, Makoto
    Fukuda, Keiichi
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2010, 49 (04) : 576 - 586
  • [40] Macelignan protects against renal ischemia-reperfusion injury via of inhibition inflammation and apoptosis of renal epithelial cells
    Long, Jianhua
    Qian, Kun
    Tan, Shubo
    Liu, Jia
    Li, Jianjun
    CELLULAR AND MOLECULAR BIOLOGY, 2020, 66 (01) : 55 - 59