Zhejiang Academy of Medical Sciences, Hangzhou Medical College, Hangzhou, China.
Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou, China.
Pharm Biol. 2020 Dec;58(1):276-285. doi: 10.1080/13880209.2020.1742167.
Shenmai Injection (SMI) is usually used to treat atherosclerotic coronary heart disease and viral myocarditis in China. However, the effect of SMI on multidrug resistance has not been reported. To investigate the reversal effect of SMI in adriamycin (ADR) resistant breast cancer cell line (MCF-7/ADR) and explore the related molecular mechanisms. The effect of SMI (0.25, 0.5, 1 mg/mL) to reverse chemoresistance in MCF-7/ADR cells was elucidated by MTT, HPLC-FLD, DAPI staining, flow cytometric analysis, western blotting. At the same time, test was conducted to probe into the effect of SMI on reversing ADR resistance, and verapamil (10 μM) was used as a positive control. The results showed that the toxicity of ADR to MCF-7/ADR cells was strengthened significantly after treated with SMI (0.25, 0.5, 1 mg/mL), the IC of ADR was decreased 54.4-fold. The intracellular concentrations of ADR were increased 2.2-fold ( < 0.05) and ADR accumulation was enhanced in the nuclei ( < 0.05). SMI could strongly enhance the ADR-induced apoptosis and increase intracellular rhodamine 123 accumulation in MCF-7/ADR cells. Additionally, a combination of ADR and SMI (5 mg/kg) could dramatically reduce the weight and volume of tumour ( < 0.05). Furthermore, the results revealed that SMI might reverse MDR via inhibiting ADR-induced activation of the mitogen-activated protein kinase/nuclear factor (NF)-κB pathway to down-regulated the expression of P-glycoprotein (P-gp). SMI could potentially be used to treat ADR-resistance. This suggests possibilities for future clinical research.
参麦注射液(SMI)通常用于治疗中国的动脉粥样硬化性冠心病和病毒性心肌炎。然而,SMI 对多药耐药性的影响尚未报道。为了研究 SMI 在阿霉素(ADR)耐药乳腺癌细胞系(MCF-7/ADR)中的逆转作用,并探讨相关的分子机制。通过 MTT、HPLC-FLD、DAPI 染色、流式细胞术分析和 Western blot 研究了 SMI(0.25、0.5、1mg/ml)对 MCF-7/ADR 细胞化学耐药性的逆转作用。同时,进行了测试,以探讨 SMI 对逆转 ADR 耐药性的影响,并用维拉帕米(10μM)作为阳性对照。结果表明,SMI(0.25、0.5、1mg/ml)处理后,ADR 对 MCF-7/ADR 细胞的毒性明显增强,ADR 的 IC 降低了 54.4 倍。细胞内 ADR 浓度增加了 2.2 倍( < 0.05),ADR 蓄积增强于核内( < 0.05)。SMI 能强烈增强 ADR 诱导的细胞凋亡,增加 MCF-7/ADR 细胞内罗丹明 123 的蓄积。此外,ADR 和 SMI(5mg/kg)联合使用可显著降低肿瘤的重量和体积( < 0.05)。此外,结果表明 SMI 可能通过抑制 ADR 诱导的丝裂原活化蛋白激酶/核因子(NF)-κB 通路的激活来逆转 MDR,从而下调 P-糖蛋白(P-gp)的表达。SMI 可能有潜力用于治疗 ADR 耐药性。这为未来的临床研究提供了可能性。
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