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先前暴露于低剂量适应性辐射对具有不同Trp53功能的胎鼠辐射诱导致畸效应的影响。

Influence of prior exposure to low-dose adapting radiation on radiation-induced teratogenic effects in fetal mice with varying Trp53 function.

作者信息

Mitchel R E J, Dolling J-A, Misonoh J, Boreham D R

机构信息

Radiation Biology and Health Physics Branch, Atomic Energy of Canada Limited, Chalk River Laboratories, Ontario, K0J 1J0 Canada.

出版信息

Radiat Res. 2002 Oct;158(4):458-63. doi: 10.1667/0033-7587(2002)158[0458:iopetl]2.0.co;2.

Abstract

Teratogenesis in tails and limb digits of fetal mice with varying Trp53 status was examined after exposure of pregnant females to 4 Gy gamma radiation with and without a prior 30-cGy exposure. Prior low-dose exposure modified the teratogenic effects of radiation in a manner dependent upon Trp53 status and gestation time. A 4-Gy exposure on gestation day 11 resulted in tail shortening and digit abnormalities. A 30-cGy exposure 24 h prior to a 4-Gy radiation exposure on day 11 reduced the extent of both digit abnormalities and the tail-shortening effects in Trp53(+/+) fetuses and also reduced tail shortening in Trp53(+/-) fetuses, but to a lesser extent. However, the pre-exposure enhanced the tail-shortening effects of 4 Gy in Trp53(-/-) fetuses. In contrast, a 30-cGy exposure given 24 h prior to a 4-Gy exposure on gestation day 12 had no effect on the reduced tail length resulting from the 4-Gy exposure of Trp53(+/+) or Trp53(+/-) fetuses, but it partly protected Trp53(-/-) fetuses against reduced tail length. A 4-Gy exposure alone on day 12 did not result in any increase in the frequency of digit abnormalities in Trp53(-/-) fetuses so any protective effect of the preirradiation could not be detected. However, the preirradiation did result in protection against in digit abnormalities in Trp53(+/-) fetuses. We conclude that radiation-induced teratogenesis reflects both Trp53-dependent and independent processes that lead to apoptosis, and these respond differently to prior adapting doses.

摘要

在怀孕母鼠分别接受4 Gy γ射线照射(有无30 cGy的预照射)后,研究了不同Trp53状态的胎鼠尾巴和肢端指骨的致畸情况。预先的低剂量照射以一种依赖于Trp53状态和妊娠时间的方式改变了辐射的致畸效应。妊娠第11天接受4 Gy照射会导致尾巴缩短和指骨异常。在第11天4 Gy辐射照射前24小时给予30 cGy照射,可减少Trp53(+/+)胎鼠的指骨异常程度和尾巴缩短效应,也可减少Trp53(+/-)胎鼠的尾巴缩短效应,但程度较小。然而,预照射增强了Trp53(-/-)胎鼠4 Gy照射的尾巴缩短效应。相比之下,在妊娠第12天4 Gy照射前24小时给予30 cGy照射,对Trp53(+/+)或Trp53(+/-)胎鼠因4 Gy照射导致的尾巴长度缩短没有影响,但它部分保护了Trp53(-/-)胎鼠的尾巴长度不缩短。第12天单独进行4 Gy照射不会导致Trp53(-/-)胎鼠指骨异常频率增加,因此无法检测到预照射的任何保护作用。然而,预照射确实对Trp53(+/-)胎鼠的指骨异常起到了保护作用。我们得出结论,辐射诱导的致畸反映了导致细胞凋亡的Trp53依赖性和非依赖性过程,并且这些过程对先前的适应性剂量反应不同。

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