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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Cytoprotective and antigenotoxic potential of Mangiferin, a glucosylxanthone against cadmium chloride induced toxicity in HepG2 cells.
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Cytoprotective and antigenotoxic potential of Mangiferin, a glucosylxanthone against cadmium chloride induced toxicity in HepG2 cells.

机译:Mangiferin是一种抗氯化镉的葡糖基黄酮,具有细胞保护和抗原毒性的潜力,可诱导HepG2细胞毒性。

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摘要

Mangiferin (MGN), a glucosylxanthone present in large amounts in the leaves and edible mango fruits of Mangifera indica. Here, we report about MGN's potential for mitigating cadmium chloride (CdCl(2)) induced cytotoxic and genotoxic effects in HepG2 cells growing in vitro. The cytoprotective potential was assessed by MTT, clonogenic and apoptotic assays, while antigenotoxic effect by micronucleus and comet assay. The established cytotoxic and genotoxic effects were well indicated after CdCl(2) treatment and was mitigated by pretreatment with MGN. MGN prior to CdCl(2) treatment increased the cell survival (MTT), surviving fraction (clonogenic assay) and inhibited sub-G(1) population (flow cytometric analysis). Further, inhibition of CdCl(2) induced apoptotic cell death by MGN was confirmed by microscopic and DNA fragmentation assays. A significant (p<0.01) reduction in the micronuclei frequency and comet parameters after MGN pretreatment to CdCl(2) clearly indicated the antigenotoxic potential. Similarly, the reactive oxygen species generated by the CdCl(2) treatment were inhibited significantly (p<0.001) by MGN. Taken together, our study revealed that MGN has potent cytoprotective and antigenotoxic effect against CdCl(2) induced toxicity in HepG2 cell line and which may be attributed to decrease in CdCl(2) induced reactive oxygen species levels and resultant oxidative stress.
机译:Mangiferin(MGN),一种存在于印度芒果(Mangifera indica)的叶子和可食用芒果果实中的葡萄糖基s吨酮。在这里,我们报告有关MGN的潜力,以减轻氯化镉(CdCl(2))诱导的HepG2细胞体外生长的细胞毒性和遗传毒性作用。通过MTT,克隆形成和凋亡分析评估细胞保护潜力,同时通过微核和彗星分析评估抗原毒性作用。 CdCl(2)处理后,已明确表明已建立的细胞毒性和遗传毒性作用,并通过MGN预处理得到缓解。 CdCl(2)处理之前的MGN增加细胞存活率(MTT),存活分数(克隆形成测定)和抑制sub-G(1)种群(流式细胞仪分析)。此外,通过显微镜和DNA片段测定法证实了MGN对CdCl(2)诱导的凋亡细胞死亡的抑制作用。 MGN预处理CdCl(2)后,微核频率和彗星参数的显着(p <0.01)减少清楚地表明了其潜在的抗原毒性。同样,由CdCl(2)处理产生的活性氧被MGN显着抑制(p <0.001)。综上所述,我们的研究表明MGN对HepG2细胞系中的CdCl(2)诱导的毒性具有有效的细胞保护作用和抗原毒性作用,这可能归因于CdCl(2)诱导的活性氧水平降低和由此产生的氧化应激。

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