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Absence of genomic instability in mice following prenatal low dose-rate gamma-irradiation.

机译:产前低剂量率伽马射线辐照后小鼠中没有基因组不稳定。

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摘要

PURPOSE: To determine whether mice exposed to an extended low dose of gamma-irradiation during most of their prenatal period express increased frequencies of micronucleated polychromatic erythrocytes (fMPCE) and/or micronucleated normochromatic erythrocytes (fMNCE) several weeks after the end of irradiation. METHODS: Female CBA/Ca mice were gamma-irradiated for an average of 16 days during their pregnancy. The mice were exposed to dose rates of 0, 44, 99 and 265 mGy/day. At 1-2 days prior to parturition the mice were removed from exposure. Then, 36 days after birth, peripheral blood was drawn from all offspring (74 mice). Using flow-cytometer-based analysis, the frequencies of MPCE and MNCE were determined. From each animal about 170,000 PCE were analysed. RESULTS: No delayed effects in terms of higher fMPCE or fMNCE were observed among the in utero exposed mice of either gender. On the contrary, a significant (p<0.001) reduction of fMPCE was found among the male offspring exposed at the highest dose rate. CONCLUSION: Gamma-irradiation of mice during their prenatal stage did not induce damage in erythroid stem cells that can be detected as persistent or delayed chromosome aberrations (i.e. micronucleated erythrocytes) at 35 days after the end of exposure.
机译:目的:确定在辐照结束后几周内,在大部分产前期长期接受低剂量γ-辐射照射的小鼠中微核多色红细胞(fMPCE)和/或微核正色红细胞(fMNCE)的频率是否增加。方法:雌性CBA / Ca小鼠在怀孕期间平均接受了16天的γ射线照射。小鼠暴露于0、44、99和265mGy /天的剂量率。在分娩前1-2天,将小鼠从暴露中移出。然后,在出生后36天,从所有后代(74只小鼠)抽取外周血。使用基于流式细胞仪的分析,确定了MPCE和MNCE的频率。从每只动物中分析出约170,000 PCE。结果:在任何性别的子宫内暴露的小鼠中,未观察到较高的fMPCE或fMNCE的延迟作用。相反,在以最高剂量率暴露的雄性后代中发现fMPCE显着降低(p <0.001)。结论:在产前阶段对小鼠进行伽马射线辐照不会引起红系干细胞的损伤,在暴露结束后的35天,可以将其检测为持续或延迟的染色体畸变(即微核红细胞)。

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