Yang Huihai, Li Wei, Wang Lulu, Li Wenqing, Sun Hang, He Xiaofeng, Zhang Jing
Department of Traditional Chinese Pharmacology, College of Traditional Chinese Medicine, Jilin Agricultural University, Changchun, China.
Department of Traditional Chinese Pharmacology, College of Medicine, Changchun Science- Technology University, Changchun, China.
Cell Physiol Biochem. 2017;43(1):395-404. doi: 10.1159/000480418. Epub 2017 Aug 31.
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.
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.
Pretreatment with SDAPR (125-2000 µg/mL) significantly improved cell viability, with an EC50 of approximately 1000 µg/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).
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.
背景/目的:本研究测定了梅花鹿(Cervus nippon Temminck)鹿茸蛋白(SDAPR)、糖蛋白(SDAG)和多糖(SDAPO)对顺铂诱导的HEK 293细胞毒性的影响,并研究了SDAPR对顺铂诱导的小鼠肾毒性的作用。
采用MTT法测定细胞活力。将ICR小鼠随机分为五组:对照组、顺铂加赋形剂组、顺铂加三种浓度(5、10或20 mg/kg,口服,共10天)的SDAPR组。在第7天腹腔注射顺铂(25 mg/kg)。在体内测定肾功能、氧化应激、炎症因子水平和凋亡相关蛋白的表达。用TUNEL和苏木精-伊红染色观察肾组织细胞凋亡和病理变化。
用SDAPR(125 - 2000 µg/mL)预处理可显著提高细胞活力,半数有效浓度(EC50)约为1000 µg/mL。SDAPR还改善了顺铂诱导的组织病理学变化,并降低了血尿素氮(BUN)和肌酐(Cr)水平(P < 0.05)。蛋白质印迹分析显示,SDAPR明显降低了裂解的半胱天冬酶-3和Bax的表达水平,并增加了Bcl-2的表达水平(P < 0.01)。此外,SDAPR显著调节氧化应激标志物和炎症细胞因子(P < 0.05)。TUNEL染色显示SDAPR处理后细胞凋亡减少(P < 0.01)。
这些结果表明,SDAPR可以作为一种有效的膳食补充剂,通过提高抗氧化酶活性、抑制炎症和抑制体内细胞凋亡来减轻顺铂诱导的肾毒性。