显著增加显性致死突变:苯并(a)芘

S. M, Sadasivan Sadasivan, Chanderasekharan Chanderasekharan, Yoganand Moolemath, Anup M Oomme
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摘要

背景:生物标志物的使用在风险评估中具有重要意义,尤其是在体内条件下。本研究旨在通过显性致死突变试验,确定暴露于B(a)P的姜黄喂养动物的体内抗毒素潜力,并评价姜黄在对抗生殖细胞突变中的作用。方法:雄性小鼠24只,随机分为4组,每组6只。第一组和第二组饲喂普通饲粮(对照),第三组和第四组饲喂5%姜黄饲粮,试验期1个月。饲喂期结束时,第二组和第四组小鼠腹腔注射单剂量苯并(a)芘1mg/只。1周后,每只雄鼠按1、4、8和12周的间隔与3只雌鼠交配。交配中期后第13天处死雌性,计数活胚和死胚,研究着床前和着床后胚胎丢失情况。采用方差分析(ANOVA)和卡方检验比较治疗组、阳性对照和阴性对照,比较治疗组与对照组在4个时间段内种植前后死亡频率的差异。结果:与对照组相比,饲喂5%姜黄和单剂量B(a)P处理组对致突变指数和妊娠率无显著影响。B(a)P或B(a)P+姜黄处理组未明显诱导显性致死突变。本研究未发现B(a)P在植入后产生显性致死效应。B(a)P的诱导和姜黄处理不影响显性致死试验。结论:B(a)P未显著增加显性致死突变。姜黄也没有任何积极的反应,可能被认为是非诱变的。阴性结果表明,在试验条件下,试验物质在试验物种的处理性别的生殖细胞中可能没有遗传毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Significant increase in the dominant lethal mutations: benzo(a)pyrene
Background: Use of biomarkers particularly under in vivo condition is of importance in risk assessment. This study is proposed to identify the in vivo antigenotoxic potential using dominant lethal mutation test in B(a)P exposed, turmeric fed animals and evaluate the role of turmeric in counteracting the germ cell mutations. Methods: Twenty four male mice were taken and divided into 4 groups each group containing 6 mice/group. The first and second group received stock diet (control) while the third and fourth groups received 5% turmeric diet for a period of one month. At the end of feeding period, second and fourth group received a single dose of benzo(a)pyrene 1mg/mouse intraperitoneally. After 1 week each male mouse was mated to 3 female mice at 1,4, 8 and 12 week intervals. On 13th day from mid point of mating, the females were sacrificed and live and dead embryos were counted to study the pre and post implantation loss of embryos. The differences in the frequencies of pre and post implant deaths were done by comparing treated with control group at 4-time periods by analysis of variance (ANOVA) and chi-square test which is used to compare treatment group and positive control with negative control. Results: Feeding of 5% turmeric and treatment with a single dose of B(a)P did not show any significant effect on the mutagenic index or the frequency of pregnancy in treated groups compared with control. There was no apparent induction of dominant lethal mutations in B(a)P or B(a)P+Turmeric treated groups. No post implantation dominant lethal effects produced by B(a)P could be detected in this study. The induction of B(a)P and treatment with turmeric did not influence the dominant lethal test. Conclusion: B(a)P did not produce a significant increase in the dominant lethal mutations. Turmeric also did not give any positive response and may be considered as non-mutagenic. The negative result suggests that under the conditions of the test the test substance may not be genotoxic in the germ cell of the treated sex of the test species.
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