Shenduning Granule Attenuates Renal Injury from Oxidative Stress through the Nuclear Factor Erythroid 2-Related Factor 2/Antioxidant Response Element Pathway

被引:9
|
作者
Fu, Xiao-Jun [1 ]
Hu, Shuang-Yan [1 ]
机构
[1] Jinhua Hosp Tradit Chinese Med, Dept Nephropath, Jinhua, Peoples R China
关键词
Chronic kidney disease oxidative stress; Shenduning granule; Nuclear factor erythroid 2-related factor 2; Heme oxygenase-1; gamma-glutamyl-cysteine synthetase; TRANSCRIPTION FACTOR; HEME OXYGENASE-1; GENE-EXPRESSION; UP-REGULATION; SUBUNIT GENE; NRF2; ANTIOXIDANTS; INDUCTION; APOPTOSIS; DEFENSE;
D O I
10.1159/000494981
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Systemic oxidative stress has been reported to play a central role in the pathogenesis of kidney function decline. The nuclear factor erythroid 2-related factor 2 (Nrf2)/antioxidant response element (ARE) pathway is one of the important endogenous antioxidant stress pathways in cells. This study aims to investigate whether shenduning granule can ameliorate oxidative stress in kidney tissues by activating the Nrf2/ARE pathway, and explores the detailed underlying mechanism. Methods: A total of 120 male SpragueDawley rats were randomly assigned to the sham-operated and operation groups. Rats in the operation group underwent 5/6 nephrectomy. Two weeks later, rats in the operation group were further randomly divided into 5 groups: model group, low-dose, medium-dose and high-dose shenduning granule groups, and losartan group. Rats in each group were given the same volume of corresponding liquid orally. Serum creatinine (SCr), blood urea nitrogen (BUN), 24-h urinary protein, malondialdehyde (MDA) and superoxide dismutase (SOD), Nrf2, heme oxygenase-1 (HO-1), and gamma-glutamyl-cysteine synthetase (gamma-GCS) were determined. Results: Shenduning granule could markedly elevate HO-1, NRF2, gamma-GCS and SOD (p < 0.05), and significantly decreased MDA, 24-h urinary protein, SCr and BUN in rats (p < 0.05). Conclusion: Shenduning granule can improve renal antioxidative stress activity in rats, exhibiting a renoprotective effect. The potential mechanism is likely exerted by the activation of the Nrf2/ARE pathway. (c) 2019 S. Karger AG, Basel
引用
收藏
页码:236 / 245
页数:10
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