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首页> 外文期刊>Antioxidants and redox signalling >Functional consequences of radiation-induced oxidative stress in cultured neural stem cells and the brain exposed to charged particle irradiation
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Functional consequences of radiation-induced oxidative stress in cultured neural stem cells and the brain exposed to charged particle irradiation

机译:辐射诱导的神经干细胞和暴露于带电粒子辐射的大脑中氧化应激的功能后果

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摘要

Aims: Redox homeostasis is critical in regulating the fate and function of multipotent cells in the central nervous system (CNS). Here, we investigated whether low dose charged particle irradiation could elicit oxidative stress in neural stem and precursor cells and whether radiation-induced changes in redox metabolism would coincide with cognitive impairment. Results: Low doses (<1 Gy) of charged particles caused an acute and persistent oxidative stress. Early after (<1 week) irradiation, increased levels of reactive oxygen and nitrogen species were generally dose responsive, but were less dependent on dose weeks to months thereafter. Exposure to ion fluences resulting in less than one ion traversal per cell was sufficient to elicit radiation-induced oxidative stress. Whole body irradiation triggered a compensatory response in the rodent brain that led to a significant increase in antioxidant capacity 2 weeks following exposure, before returning to background levels at week 4. Low dose irradiation was also found to significantly impair novel object recognition in mice 2 and 12 weeks following irradiation. Innovation: Data provide evidence that acute exposure of neural stem cells and the CNS to very low doses and fluences of charged particles can elicit a persisting oxidative stress lasting weeks to months that is associated with impaired cognition. Conclusions: Exposure to low doses of charged particles causes a persistent oxidative stress and cognitive impairment over protracted times. Data suggest that astronauts subjected to space radiation may develop a heightened risk for mission critical performance decrements in space, along with a risk of developing long-term neurocognitive sequelae. Antioxid.
机译:目的:氧化还原稳态对于调节中枢神经系统(CNS)中多能细胞的命运和功能至关重要。在这里,我们研究了低剂量带电粒子辐照是否会在神经干细胞和前体细胞中引发氧化应激,以及辐射诱发的氧化还原代谢变化是否与认知障碍一致。结果:低剂量(<1 Gy)的带电粒子会引起急性和持续的氧化应激。辐照后(<1周)的早期,活性氧和氮物种水平的升高通常具有剂量响应性,但对剂量周至数月的依赖性较小。暴露于离子注量下导致每个细胞的离子穿越量不足一次,足以引起辐射诱导的氧化应激。全身照射在啮齿动物的大脑中引发了补偿性反应,导致暴露后2周抗氧化能力显着增加,然后在第4周恢复至本底水平。还发现,低剂量辐照还显着损害了小鼠2和3的新物体识别。照射后12周。创新:数据提供的证据表明,神经干细胞和中枢神经系统急性暴露于非常低的剂量和带电粒子通量可以引发持续数周至数月的持续氧化应激,这与认知能力下降有关。结论:长时间暴露于低剂量带电粒子会导致持续的氧化应激和认知障碍。数据表明,受到空间辐射的宇航员可能会增加太空中关键任务性能下降的风险,同时还会出现长期的神经认知后遗症。抗氧化。

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