Bandyopadhyay Atrayee, Ghoshal Sarbani, Mukherjee Anita
Centre of Advanced Study, Cell and Chromosome Research, Department of Botany, University of Calcutta, Kolkata, India.
Drug Chem Toxicol. 2008;31(4):447-57. doi: 10.1080/01480540802390270.
Low-calorie sweeteners are chemicals that offer the sweetness of sugar without the calories. Consumers are increasingly concerned about the quality and safety of many products present in the diet, in particular, the use of low-calorie sweeteners, flavorings, colorings, preservatives, and dietary supplements. In the present study, we evaluated the mutagenicity of the three low-calorie sweeteners in the Ames/Salmonella/microsome test and their genotoxic potential by comet assay in the bone marrow cells of mice. Swiss albino mice, Mus musculus, were orally administered with different concentrations of aspartame (ASP; 7, 14, 28, and 35 mg/kg body weight), acesulfame-K (ASK; 150, 300, and 600 mg/kg body weight), and saccharin (50, 100, and 200 mg/kg body weight) individually. Concurrently negative and positive control sets were maintained. The animals were sacrificed and the bone marrow cells were processed for comet assay. The standard plate-incorporation assay was carried with the three sweeteners in Salmonella typhimurium TA 97a and TA 100 strains both in the absence and presence of the S9 mix. The comet parameters of DNA were increased in the bone marrow cells due to the sweetener-induced DNA strand breaks, as revealed by increased comet-tail extent and percent DNA in the tail. ASK and saccharin were found to induce greater DNA damage than ASP. However, none could act as a potential mutagen in the Ames/Salmonella /microsome test. These findings are important, since they represent a potential health risk associated with the exposure to these agents.
低热量甜味剂是一类能提供糖的甜味但不含热量的化学物质。消费者越来越关注饮食中许多产品的质量和安全性,特别是低热量甜味剂、调味剂、色素、防腐剂和膳食补充剂的使用。在本研究中,我们通过Ames/沙门氏菌/微粒体试验评估了三种低热量甜味剂的诱变性,并通过彗星试验评估了它们对小鼠骨髓细胞的遗传毒性潜力。将不同浓度的阿斯巴甜(ASP;7、14、28和35毫克/千克体重)、安赛蜜-K(ASK;150、300和600毫克/千克体重)和糖精(50、100和200毫克/千克体重)分别口服给予瑞士白化小鼠(小家鼠)。同时设置阴性和阳性对照组。处死动物后,对骨髓细胞进行彗星试验处理。在有无S9混合物的情况下,用这三种甜味剂对鼠伤寒沙门氏菌TA 97a和TA 100菌株进行标准平板掺入试验。彗星试验结果显示,由于甜味剂诱导的DNA链断裂,骨髓细胞中DNA的彗星参数增加,表现为彗星尾长度增加和尾中DNA百分比增加。发现ASK和糖精比ASP诱导的DNA损伤更大。然而,在Ames/沙门氏菌/微粒体试验中,它们都不能作为潜在的诱变剂。这些发现很重要,因为它们代表了与接触这些物质相关的潜在健康风险。