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
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