Anti-thrombotic and anti-tumor effect of water extract of caulis of Sargentodoxa cuneata (Oliv) Rehd et Wils (Lardizabalaceae) in animal models

被引:3
|
作者
Chen, Hong [1 ]
Wan, Xue-mei [2 ]
Zhou, Xue-lei [3 ]
机构
[1] Chongqing Canc Hosp, Chongqing Canc Inst, Oncol Dept Tradit Chinese Med, Chongqing 400030, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Teaching Hosp, Dept Infect Dis, Chengdu 610075, Peoples R China
[3] Chengdu Univ Tradit Chinese Med, Teaching Hosp, Spleen & Stomach Dis Dept, Chengdu 610075, Peoples R China
关键词
Sargentodoxa cuneata; Anti-thrombosis; Anti-tumor; Platelet aggregation; Apoptosis; Caspase; Protocatechuic acid; Rhodiola glucoside; Chlorogenic acid; PHENOLIC GLYCOSIDES; APOPTOSIS; CELLS; THERAPY; BCL-2;
D O I
10.4314/tjpr.v15i11.13
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To investigate the anti-thrombosis and anti-tumor effect of the water extract of the caulis of Sargentodoxa cuneata (Oliv.) Rehd. et Wils. (WCSW) in rat and mouse models. Methods: WCSW extract was prepared and the main constituents were determined by high pressure liquid chromatography (HPLC). The acute toxicity of the extract was determined in mice. Platelet aggregation in rat platelet-rich plasma (PRP) was examined to evaluate the effect of the extract on platelet function. Thereafter, the cytotoxic activity of WCSW on HL60, A549, S180 and H22 cells was determined by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. In vivo antitumor effect of WCSW was further evaluated on H22 cells transplanted in mice, while the expression of caspase-3, caspase-9, Bcl-2 and Bax proteins were assayed by Western blot analysis. Results: Protocatechuic acid, rhodiola glucoside and chlorogenic acid were identified as the main constituents of WCSW. Platelet aggregation was significantly inhibited by treatment with the extract at concentrations of 1, 5 and 10 mg/mL. WCSW also showed significant inhibitory effect on HL60, A549, S180 and H22 cells in vitro with half maximal inhibitory concentration (IC50 value of 321.9, 285.0, 130.3 and 76.1 mu g/mL, respectively. Furthermore, WCSW exhibited obvious anti-tumor effect on H22 transplanted tumor in vivo. After treatment with WCSW, caspase-3, caspase-9 and Bax were significantly (p < 0.05) up-regulated, whereas Bcl-2 was significantly (p < 0.05) down-regulated in the tumor tissues. Conclusion: WCSW possesses significant antithrombosis and anti-tumor effect, and therefore, has the potentials to be developed into effective drugs for clinical treatment of cancer and thrombosis diseases.
引用
收藏
页码:2391 / 2397
页数:7
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