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Comet Assay of DNA Damage in Brain Cells of Offspring Rats Exposed to Long-term Intake High Fluoride and Low Iodine

机译:长期摄入高氟低碘的后代大鼠脑细胞DNA损伤的彗星试验

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To assess damage to DNA in their brain cells of offspring rats exposed to high fluoride and/or low iodine, 32 Wistar rats were divided randomly into four groups of eight rats (female : male=3:l). The first group of rats served as the untreated controls; the second group received high fluoride(HiF)in their drinking water(100 mg NaF/L); the third group was placed on a low iodine(LI)diet (0.0855 mg I/kg); and the fourth group was exposed to the same concentrations of HiF and LI together. After the animal model was established, the rats were allowed to breed, and 36 offspring rats in each group (female: male=l:l) were randomly selected for the experiments. At 0, 10, 20, 30, 60 and 90 day, the offspring rats were anesthetized and their brain cells prepared for single cell gel electrophoresis (SCGE=comet assay). Ratio of tailing in brain cells of 0, 10, 20, 30, 60 and 90 day-old rats in high fluoride group were 56.11%, 48.74%, 86.74%, 53.84%, 86.58%, 89.09% (average ratio, 70.18%) and the proportion of gradeⅢ damage to brain cells in 20 day-old rats is up to 85.71%. The rate and degree of DNA damage of brain cell in different age rats is higher in the HiF+LI group than in the other experimental groups. And ratio of tailing in brain cells of 0, 10, 20, 30, 60 and 90 day-old rats were 88.25%, 41.23%, 68.22%, 72.62%, 92.61%, 93.91%. These results indicate that DNA strands in the brain cells of rats from 0 day to 90day are adversely affected by exposure to high fluoride, low iodine, and together in combination. The rate and degree of DNA damage in brain cells is higher in the HiF+LI group than in either the HiF or LI group.
机译:为了评估暴露于高氟化物和/或低碘的后代大鼠脑细胞中DNA的损伤,将32只Wistar大鼠随机分为四组,每组八只大鼠(雌性:雄性= 3:1)。第一组大鼠作为未治疗的对照;第二组的饮用水中含有高氟化物(HiF)(100 mg NaF / L);第三组为低碘饮食(0.0855 mg I / kg);第四组同时暴露于相同浓度的HiF和LI。建立动物模型后,允许大鼠繁殖,并随机选择每组36只后代大鼠(雌性:雄性= 1∶1)进行实验。在0、10、20、30、60和90天时,麻醉后代大鼠,并准备其脑细胞用于单细胞凝胶电泳(SCGE =彗星试验)。高氟组0、10、20、30、60和90日龄大鼠脑细胞的拖尾率分别为56.11%,48.74%,86.74%,53.84%,86.58%,89.09%(平均比例为70.18%) ),并且在20日龄大鼠中,Ⅲ级对脑细胞的损害比例高达85.71%。 HiF + LI组不同年龄大鼠脑细胞DNA损伤的程度和程度均高于其他实验组。 0、10、20、30、60和90日龄大鼠脑细胞的拖尾率分别为88.25%,41.23%,68.22%,72.62%,92.61%,93.91%。这些结果表明,从0天到90天的大鼠脑细胞中的DNA链受到高氟化物,低碘以及它们的联合暴露的不利影响。 HiF + LI组的脑细胞中DNA损伤的速率和程度高于HiF或LI组。

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