用白花蛇舌草药剂处理可降低小鼠黑色素瘤细胞中的 MCP-1 和 ROs 水平。

Priscila Baltuille, Thaís Cristina Silva, E. C. Hurtado, C. Holandino, Stephan Baumgartner, L. Bonamin
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摘要

黑色素瘤是造成大多数皮肤癌死亡的原因。它的转移潜力大,治疗复杂,预后无望。白花蛇舌草提取物(Va)是一种辅助治疗癌症的药物,对不同类型的肿瘤具有体外和体内细胞毒性作用。然而,其超稀释顺势疗法制剂对癌细胞的作用和机制还需要进一步研究。因此,本研究的目的是调查黑色素瘤细胞在使用瑞士夏季从宿主树白叶松(VaAa)和红柞树(VaQr)中采集的超稀释顺势疗法制剂处理后的细胞因子谱和 ROs 生成情况。为此,我们使用 VaAa 和 VaQr 的母酊剂(MT)制备了不同顺势疗法浓度的 Va,并对其进行了顺势疗法乙醇浸泡和随后的动态处理。然后,用 MT 或 12DH、200CH 或 5LM 效力的 VaAa 或 VaQr 处理 24、48 或 72 小时在 24 孔板中培养的 B16F0 黑色素瘤细胞。之后收集培养上清,以评估 MCP-1、INF-γ、TNF-α、IL-10、IL-12p70 和 IL-6 细胞因子的水平以及 ROs 的产生。结果表明,与未经处理或卡铂处理的细胞相比,用 12DH 或 5LM 效价的 Va(VaQr,优先)处理的 B16F10 黑色素瘤细胞的 MCP-1 和 ROs 水平明显降低。总之,我们首次证明了按不同顺势疗法比例配制的 Va 药效对黑色素瘤细胞中细胞因子和 ROs 生成的体外效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment with Viscum album potencies induces reduction of MCP-1 and ROs levels in murine melanoma cells.
Melanoma is responsible for most skin cancer deaths. It has a high metastatic potential, complex treatment, and a hopeless prognosis. Viscum album extract (Va) is a complementary treatment in cancer, with in vitro and in vivo cytotoxic effects on different tumor types. However, its ultra-diluted homeopathic preparations' effects and mechanisms on cancer cells need further study. Thus, the aim of present work was to investigate cytokine profile and ROs production of melanoma cells after treatment with ultradiluted VA collected from host tree Abies alba (VaAa) and Quercus rubur (VaQr)during Swiss summer. For this, potencies of Va in different homeopathic scales were prepared using mother tincture (MT) from VaAa and VaQr submitted to homeopathic ethanolic maceration and then a subsequent dynamization process. Then, B16F0 melanoma cells cultivated in 24-well plates were treated with MT or 12DH, 200CH or 5LM potencies of VaAa or VaQr for 24, 48 or 72 hours. After these periods, culture supernatants were collected to assess the levels of MCP-1, INF-γ, TNF-α, IL-10, IL-12p70 and IL-6 cytokines and, ROs production. Results demonstrated significant reduction of MCP-1 and ROs levels in B16F10 melanoma cells treated with Va (VaQr, preferentially) at 12DH or 5LM potencies when compared to untreated or carboplatin-treated cells. In conclusion, we demonstrated for the first time, the in vitro effects of Va potencies prepared in different homeopathic scales in relation to cytokines and ROs production in cell melanoma cells.
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