非洲蒿叶提取物的评价。前Willd。和丝纹白藻Eckl。Zeyh。基因毒性和EMS诱导的基因毒性的调节

A. Okorie, S. Magama, M. Nthabiseng
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引用次数: 2

摘要

细胞凋亡和/或细胞周期阻滞、细胞毒性、遗传毒性和抗遗传毒性等一系列短期体外试验用于筛选和确定药用植物的功效。本研究评估了三种浓度(0.1、0.2或0.4 mg/ml)的阿法蒿(Artemisia afra)和白花蒿(Leucosidea sericea)的甲醇叶提取物及其与甲磺酸乙酯(EMS) (0.15 mg/ml)的混合物在体内诱导这些终点的效果。细胞毒性细胞有丝分裂指数,测定基因毒性被表示为异常的有丝分裂细胞的数量每100人有丝分裂细胞和调节效应(我)被计算为:我= (B - C) - (A - C) / (A - C)和价值,积极或消极,表示单位数量mutagen-induced基因毒性(A),等于mixture-induced基因毒性(B)。A . afra提取的三个浓度测试不诱导细胞周期阻滞和细胞毒性。0.4 mg/ml浓度及其与EMS混合均有遗传毒性。丝蚕提取物的浓度不会引起细胞周期阻滞,对丝蚕根尖细胞没有细胞毒性和基因毒性。0.2或0.4 mg/ml蚕丝提取物与EMS混合均具有遗传毒性。0.4 mg/ml蚕丝提取物与EMS混合后的遗传毒性显著高于EMS (ME = 4.40 bb0 2)。麻风和丝蚕叶提取物缺乏细胞周期阻滞活性,无毒,但对ems诱导的遗传毒性缺乏抗基因毒性活性。高浓度的蚕丝乳杆菌具有遗传毒性,而高浓度的蚕丝乳杆菌与EMS有协同作用。观察到的染色体异常包括粘染色体、c-有丝分裂、染色体脱落、染色体片段、后期和末期桥。关键词:抗遗传毒性,细胞周期阻滞,莱索托药用植物安全性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of leaf extracts of Artemisia afra Jacq. ex Willd. and Leucosidea sericea Eckl. Zeyh. for genotoxicity and the modulation of EMS-induced genotoxicity
A battery of short-term in vitro assays for apoptosis and/or cell cycle arrest, cytotoxicity, genotoxicity and antigenotoxicity are used to screen and establish the efficacy of medicinal plants. This study evaluated three concentrations (0.1, 0.2 or 0.4 mg/ml) of methanolic leaf extracts of Artemisia afra and Leucosidea sericea and their individual mixtures with Ethyl methanesulfonate (EMS) (0.15 mg/ml) for induction of those end points using the in vivo Allium cepa assay. Cytotoxicity was measured by the mitotic index, genotoxicity was expressed as the number of aberrant mitotic cells per 100 mitotic cells and modulatory effect (ME) was calculated as: ME = (B - C) - (A - C) / (A - C) and the value, positive or negative, indicated the number of units of the mutagen-induced genotoxicity (A) that equaled the mixture-induced genotoxicity (B). The three concentrations of A. afra extract tested did not induce cell cycle arrest and were not cytotoxic. The 0.4 mg/ml concentration and its mixture with EMS were genotoxic. The concentrations of L. sericea extract tested did not induce cell cycle arrest, were not cytotoxic nor genotoxic to the A. cepa root tip cells. The mixture of either 0.2 or 0.4 mg/ml L. sericea extract with EMS was genotoxic. The mixture of 0.4 mg/ml L. sericea extract with EMS was significantly more (ME = 4.40>2) genotoxic than EMS alone. Leaf extracts of A. afra and L. sericea lacked cell-cycle arrest activity, were non-toxic but lacked antigenotoxic activity against EMS-induced genotoxicity. High concentrations of A. afra were genotoxic whereas high concentrations of L. sericea interacted synergistically with EMS. Chromosomal abnormalities observed included sticky chromosomes, c-mitosis, chromosome largards, chromosome fragments, anaphase and telophase bridges.    Key words: Anti-genotoxicity, cell cycle arrest, safety of medicinal plants of Lesotho.
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