Antioxidant and cytotoxic potential of potentized preparation of Cordyceps sinensis in vitro in cancer cell lines
Q3 Medicine
Vettrivel Arul, R. Kandasamy, Marynick Sp
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引用次数: 0
Abstract
Background: The parasitic fungus Cordyceps sinensis (Ophiocordyceps sinensis) has been discovered in lepidopteran larvae, having known antitumor effects. Testing potentized Cordyceps sinensis in cancer cells could help broaden Homoeopathy cancer therapeutics. Objectives: The objectives of the study were to evaluate the antioxidant and cytotoxicity activity of potentized preparation of Cordyceps sinensis in carcinoma cell-lines. Methods: In this in vitro study, antioxidant activity was analyzed by the 2,2-diphenyl-1-picryl-hydrazylhydrate assay and the dilution with more antioxidant potential was further analyzed for cytotoxicity, using 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyltetrazolium bromide assay on various carcinoma cell lines: Breast cancer cell line (MCF-7), liver cancer cell line (HePG2), lung cancer cell line (A-549), and prostate cancer cell line (PC3). All experiments were carried out in triplicates. Data were analyzed by one-way analysis of variance and the means were compared by Duncan’s new multiple range test. Results: A higher antioxidant potential 377.40 μL/mL was seen in Cordyceps sinensis 30C, which was further analyzed for cytotoxicity in cell lines (MCF-7), (HePG2), (A-549), and (PC3) which it inhibited at concentrations 596.21 ± 3.32 μL/mL, 438.10 ± 2.39 μL/mL, 555.40 ± 3.08 μL/mL, and 656.42 ± 2.68 μL/ mL, respectively. When comparing Cordyceps sinensis 30C to other cell lines, its cytotoxic activity against HEPG2 is particularly potent. Conclusion: This research demonstrates the usefulness of potentized preparation of Cordyceps sinensis, it will take additional studies comparing it to currently used drugs to determine whether or not it is significantly more efficient. Acknowledgments and Source of Funding The authors are thankful to Alpha Omega Research Foundation, Salem, Tamil Nadu for the facilities provided. This original article is available in Indian Journal of Research in Homoeopathy: https://www.ijrh.org/journal/vol17/ iss1/2 3 © 2023 Indian Journal of Research in Homoeopathy | Hosted online by Digital Commons (Bepress) Abstract Original Article
冬虫夏草强化制剂体外对癌细胞的抗氧化和细胞毒性研究
背景:寄生真菌冬虫夏草(Ophiocordyceps sinensis)已在鳞翅目幼虫中发现,具有已知的抗肿瘤作用。在癌细胞中测试潜在的冬虫夏草可能有助于拓宽顺势疗法的癌症治疗。目的:研究冬虫夏草增强制剂对癌细胞的抗氧化活性和细胞毒活性。方法:采用2,2-二苯基-1-picryl-hydrazylhydrate法分析其体外抗氧化活性,并采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑法分析其体外抗氧化活性对乳腺癌细胞系(MCF-7)、肝癌细胞系(HePG2)、肺癌细胞系(A-549)和前列腺癌细胞系(PC3)的细胞毒性。所有的实验都是分三次进行的。数据分析采用单因素方差分析,均数比较采用Duncan新多元极差检验。结果:冬虫夏草30C对MCF-7、HePG2、A-549和PC3细胞株的抗氧化能力分别为596.21±3.32 μL/mL、438.10±2.39 μL/mL、555.40±3.08 μL/mL和656.42±2.68 μL/mL,抗氧化能力为377.40 μL/mL。将冬虫夏草30C与其他细胞系进行比较,发现其对HEPG2的细胞毒活性特别强。结论:本研究证实了冬虫夏草强化制剂的有效性,还需要进一步的研究将其与目前使用的药物进行比较,以确定其是否明显更有效。作者感谢Alpha Omega研究基金会,Salem, Tamil Nadu提供的设施。这篇原创文章可以在印度顺势疗法研究杂志上找到:https://www.ijrh.org/journal/vol17/ iss1/2 3©2023印度顺势疗法研究杂志|由Digital Commons (Bepress)在线托管摘要原创文章
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