车前草水提物体外抗肿瘤活性及体内微核遗传毒性研究

Eman Ali H. Al-Mosawie, Worood K. S. Al-Maliky
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摘要

本研究旨在评价杉木水提物对48只雌性白化小鼠体内微核形成的影响,并了解药物CCl4对微核形成的影响。将小鼠分为8组,腹腔注射7 d,第一组阴性对照组、第二组阳性对照组(CCl4 0.02%)、第三组水提取物(250 mg/kg)、第四组水提取物(500 mg/kg)、第五组(CCl4 0.02%)加水提取物(250 mg/kg)、第六组(CCl4 0.02%)加水提取物(500 mg/kg)、第七组水提取物(250 mg/kg)加(CCl4 0.02%)、第八组水提取物(500 mg/kg)加(CCl4 0.02%)。遗传-细胞方面涉及测量小鼠骨髓细胞微核形成系数的CCl4和植物水提取物处理。结果表明,与阴性对照组相比,用该药治疗小鼠导致微核形成系数升高。此外,在植物使用浓度为250 μg/ml和500 μg/ml时,植物提取物与药物之间的总重叠量显示出降低药物CCl4效应的能力,并减少微核的形成。在HepG2(肝癌细胞系)和WRL68(人肝细胞系)中,采用浓度分别为25、50、100、200和400 μg /ml的水提物对肝癌细胞系进行细胞毒性评价。结果表明,细胞活力随水提物浓度的变化而降低。癌细胞活力随浓度的增加而降低;水提物对癌细胞的活性在400 μg/ml时最低(45.34±4.44),在25 μg/ml时最高(84.53±2.41)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-tumor Activity of Plantago lanceolata Aqueous Extract In Vitro and Genotoxicity by Micronucleus Assay In Vivo
The study is designed to evaluate the effect of the aqueous extract of the P. lanceolata plant, as well as to know the effect of the drug CCl4 on the formation of micronucleus in vivo 48 female albino mice. In the study mice were separated into eight groups treated intraperitoneally for seven day first group Negative control, second positive control( CCl4 0.02%), third group aqueous extract (250 mg/kg), fourth group  aqueous extract (500 mg/kg), fifth group (CCl4 0.02%) plus aqueous extract (250 mg/kg), sixth group (CCl4 0.02%) plus aqueous extract (500 mg/kg), seventh group aqueous extract (250 mg/kg) plus (CCl4 0.02%), and eighth group aqueous extract (500 mg/kg) plus (CCl4 0.02%). The genetic-cellular aspect involved measuring the coefficient of micronucleus formation in bone marrow cells in mice treated with CCl4 and plant aqueous extract. The results showed that the treatment of mice with the drug led to a rise in the coefficient of micronucleus formation compared to the negative control group. In addition, it showed the plant's ability to reduce the drug CCl4 effect in the totals of overlaps between the plant extract and the drug at the concentrations used for the plant 250 and 500 μg/ml and reduce the formation of micronucleus. The cellular toxicity of the plant’s aqueous extract on the liver cancer cell line was assessed in HepG2 (liver cancer cell line) and the WRL68 (hepatic human cell line) using concentrations (25, 50, 100, 200, and 400 μg /ml) from the plant’s aqueous extract on the HepG2 liver cancer cell line. The results showed a decrease in cell viability depending on aqueous extract concentration. The vitality of cancer cells decreased with the increase in concentration; the viability of the aqueous extract of the plant on cancer cells reached the minimum at concentration 400 μg/ml 45.34±4.44, while it reached the maximum when concentration  25 μg/ml 84.53±2.41.
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