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Cytotoxic effects of aspartame on human cervical carcinoma cells

机译:阿斯巴甜对人宫颈癌细胞的细胞毒性作用

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摘要

Aspartame is used as an artificial sweetener in more than 6000 food varieties. The present study aims to determine the effects of aspartame at various concentrations on the cell viability, morphology, ROS level and DNA of human cervical carcinoma cells over two time periods of exposure. The effects of aspartame on HeLa cell viability were investigated using the sulphorhodamine-B assay (SRB assay) and flow cytometry. Alkaline comet assay was carried out to determine the possible DNA damage induced by aspartame. Mitochondria-derived reactive oxygen species (ROS) were determined using 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA). Fluorescence microscopy was used to determine the presence of apoptotic and necrotic cells following aspartame treatment. Cell viability was significantly altered following a higher concentration of aspartame exposure. Mitochondria-derived ROS increased at higher concentrations of aspartame exposure. Exposure to 10 mM and 20 mM of aspartame induced DNA fragmentation. Apoptotic and necrotic bodies were found in the range of 1–20 mM aspartame exposure. Exposure to high concentrations of aspartame may alter cell viability and morphology, and it may induce ROS generation and DNA damage in cervical carcinoma cells.
机译:阿斯巴甜在超过6000种食品中被用作人造甜味剂。本研究旨在确定不同浓度的阿斯巴甜在暴露的两个时间段内对人宫颈癌细胞的细胞活力,形态,ROS水平和DNA的影响。使用磺基罗丹明B测定(SRB测定)和流式细胞术研究了阿斯巴甜对HeLa细胞活力的影响。进行碱彗星试验以确定阿斯巴甜可能诱导的DNA损伤。使用2',7'-二氯二氢荧光素二乙酸酯(DCFH-DA)测定线粒体来源的活性氧(ROS)。阿斯巴甜处理后,使用荧光显微镜确定凋亡和坏死细胞的存在。暴露于更高浓度的阿斯巴甜后,细胞活力显着改变。暴露于更高浓度的阿斯巴甜时,线粒体来源的ROS增加。暴露于10 mM和20 mM的阿斯巴甜诱导的DNA片段化。发现凋亡和坏死体的阿斯巴甜暴露范围为1–20 mM。暴露于高浓度的阿斯巴甜可能会改变细胞活力和形态,并可能诱导子宫颈癌细胞中ROS的产生和DNA损伤。

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