The Protective Effects of Sika Deer Antler Protein on Cisplatin-Induced Nephrotoxicity

被引:18
作者
Yang, Huihai [1 ]
Li, Wei [1 ]
Wang, Lulu [2 ]
Li, Wenqing [1 ]
Sun, Hang [1 ]
He, Xiaofeng [1 ]
Zhang, Jing [1 ]
机构
[1] Jilin Agr Univ, Coll Tradit Chinese Med, Dept Tradit Chinese Pharmacol, Xincheng Rd 2888, Changchun 136000, Jilin, Peoples R China
[2] Changchun Sci Technol Univ, Coll Med, Dept Tradit Chinese Pharmacol, Changchun, Jilin, Peoples R China
关键词
Oxidative stress; Apoptosis; Inflammation; Renal protection; LIPID-PEROXIDATION; OXIDATIVE STRESS; KIDNEY INJURY; RENAL INJURY; ACTIVATION; MECHANISMS; APOPTOSIS; PATHWAYS; EXTRACT; DAMAGE;
D O I
10.1159/000480418
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: This study measured the effect of Sika deer (Cervus nippon Temminck) antler protein (SDAPR), glycoproteins (SDAG), and polysaccharides (SDAPO) on cisplatin-induced cytotoxicity in HEK 293 cells, and investigated the effect of SDAPR against cisplatin-induced nephrotoxicity in mice. Methods: Cell viability was measured by MTT assay. ICR mice were randomly divided into five groups: control, cisplatin with vehicle, and cisplatin with SDAPR at three concentrations: 5, 10, or 20 mg/kg, p.o., 10 d. Cisplatin was injected on 7th day (25 mg/kg, i.p.). Renal function, oxidative stress, levels of inflammatory factors, and expression of apoptosis-related proteins were measured in vivo. Renal tissues were stained with TUNEL and H&E to observe renal cell apoptosis and pathological changes. Results: Pretreatment with SDAPR (125-2000 mu g/mL) significantly improved cell viability, with an EC50 of approximately 1000 mu g/mL. SDAPR also ameliorated cisplatin-induced histopatholo-gic changes, and decreased blood urea nitrogen (BUN) and creatinine (Cr) (P < 0.05). Western blotting analysis showed SDAPR clearly decreased expression levels of cleaved-caspase-3 and Bax, and increased the expression level of Bcl-2 (P < 0.01). Additionally, SDAPR markedly regulated oxidative stress markers and inflammatory cytokines (P<0.05). TUNEL staining showed decreased apoptosis after SDAPR treatment (P < 0.01). Conclusions: These results indicate that SDAPR can be an effective dietary supplement, to relieve cisplatin-induced nephrotoxicity by improved antioxidase activity, suppressed inflammation, and inhibited apoptosis in vivo. (C) 2017 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:395 / 404
页数:10
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