Tseng Bertrand P, Giedzinski Erich, Izadi Atefeh, Suarez Tatiana, Lan Mary L, Tran Katherine K, Acharya Munjal M, Nelson Gregory A, Raber Jacob, Parihar Vipan K, Limoli Charles L
1 Department of Internal Medicine, Duke University Medical Center , Durham, North Carolina.
Antioxid Redox Signal. 2014 Mar 20;20(9):1410-22. doi: 10.1089/ars.2012.5134. Epub 2013 Aug 12.
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.
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.
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.
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.
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。在此,我们研究了低剂量带电粒子辐射是否会在神经干细胞和前体细胞中引发氧化应激,以及辐射诱导的氧化还原代谢变化是否与认知障碍相一致。
低剂量(<1 Gy)的带电粒子会引起急性且持续的氧化应激。照射后早期(<1周),活性氧和氮物种水平的升高通常呈剂量反应性,但在此后数月则对剂量的依赖性较小。暴露于导致每个细胞少于一次离子穿越的离子通量足以引发辐射诱导的氧化应激。全身照射在啮齿动物大脑中引发了一种代偿反应,导致暴露后2周抗氧化能力显著增加,然后在第4周恢复到背景水平。还发现低剂量照射在照射后2周和12周会显著损害小鼠的新物体识别能力。
数据提供了证据,表明神经干细胞和中枢神经系统急性暴露于极低剂量和通量的带电粒子可引发持续数周数月的氧化应激,这与认知障碍相关。
暴露于低剂量带电粒子会在较长时间内导致持续的氧化应激和认知障碍。数据表明,遭受太空辐射的宇航员在太空中关键任务表现下降的风险可能会增加,同时还存在出现长期神经认知后遗症的风险。