子宫内电离辐射照射与代谢调节:未来多代和跨代影响研究的前景。

Stéphane Grison, Ignacia Iii Braga-Tanaka, Sarah Baatout, Dmitry Klokov
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引用次数: 0

摘要

目的:辐射防护界一直特别关注低剂量或低剂量率电离辐射辐照对后代的延迟影 响风险。尽管如此,目前的流行病学研究和科学数据仍不足以为改进风险评估指南提供必要的证据。本文献综述旨在为今后有关多代和跨代影响的研究提供信息。它主要关注涉及子宫内暴露的动物研究,并讨论了解释研究结果的关键因素。这些要素包括与胚胎/胎儿发育阶段相关的子宫内暴露情景,以及将遗传或遗传效应传递给后代的主要生物机制。本综述探讨了多代效应和跨代效应背景下的几个问题,重点从遗传角度进行分析:健康与疾病的发育起源(DOHaD)领域的知识整合促使我们提出了一种新的研究策略。该策略旨在研究子宫内低剂量和低剂量率辐射的跨代影响。在这一概念中,胚胎和胎儿细胞的表观遗传编程可能会发生中断。这种破坏可能导致新陈代谢功能失调,进而导致对未来环境挑战的异常反应,从而增加患病风险。最后,我们讨论了研究方法上的局限性。这些局限性与队列规模、随访时间、模型辐射敏感性和分析技术有关。我们为这一领域的未来研究提出了科学和分析策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In utero exposure to ionizing radiation and metabolic regulation: perspectives for future multi- and trans-generation effects studies.

Purpose: The radiation protection community has been particularly attentive to the risks of delayed effects on offspring from low dose or low dose-rate exposures to ionizing radiation. Despite this, the current epidemiologic studies and scientific data are still insufficient to provide the necessary evidence for improving risk assessment guidelines. This literature review aims to inform future studies on multigenerational and transgenerational effects. It primarily focuses on animal studies involving in utero exposure and discusses crucial elements for interpreting the results. These elements include in utero exposure scenarios relative to the developmental stages of the embryo/fetus, and the primary biological mechanisms responsible for transmitting heritable or hereditary effects to future generations. The review addresses several issues within the contexts of both multigenerational and transgenerational effects, with a focus on hereditary perspectives.

Conclusions: Knowledge consolidation in the field of Developmental Origins of Health and Disease (DOHaD) has led us to propose a new study strategy. This strategy aims to address the transgenerational effects of in utero exposure to low dose and low dose-rate radiation. Within this concept, there is a possibility that disruption of epigenetic programming in embryonic and fetal cells may occur. This disruption could lead to metabolic dysfunction, which in turn may cause abnormal responses to future environmental challenges, consequently increasing disease risk. Lastly, we discuss methodological limitations in our studies. These limitations are related to cohort size, follow-up time, model radiosensitivity, and analytical techniques. We propose scientific and analytical strategies for future research in this field.

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