Verreet Tine, Rangarajan Janaki Raman, Quintens Roel, Verslegers Mieke, Lo Adrian C, Govaerts Kristof, Neefs Mieke, Leysen Liselotte, Baatout Sarah, Maes Frederik, Himmelreich Uwe, D'Hooge Rudi, Moons Lieve, Benotmane Mohammed A
Laboratory of Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre (SCK•CEN)Mol, Belgium; Laboratory of Neural Circuit Development and Regeneration, Animal Physiology and Neurobiology Section, Department of Biology, Faculty of Science, Katholieke Universiteit LeuvenLeuven, Belgium.
Faculty of Medicine, Molecular Small Animal Imaging Center, Katholieke Universiteit LeuvenLeuven, Belgium; Department of Electrical Engineering (ESAT/PSI), Katholieke Universiteit Leuven and Medical Image Research Center, University Hospital LeuvenLeuven, Belgium.
Front Behav Neurosci. 2016 May 4;10:83. doi: 10.3389/fnbeh.2016.00083. eCollection 2016.
Prenatal irradiation is known to perturb brain development. Epidemiological studies revealed that radiation exposure during weeks 8-15 of pregnancy was associated with an increased occurrence of mental disability and microcephaly. Such neurological deficits were reproduced in animal models, in which rodent behavioral testing is an often used tool to evaluate radiation-induced defective brain functionality. However, up to now, animal studies suggested a threshold dose of around 0.30 Gray (Gy) below which no behavioral alterations can be observed, while human studies hinted at late defects after exposure to doses as low as 0.10 Gy. Here, we acutely irradiated pregnant mice at embryonic day 11 with doses ranging from 0.10 to 1.00 Gy. A thorough investigation of the dose-response relationship of altered brain function and architecture following in utero irradiation was achieved using a behavioral test battery and volumetric 3D T2-weighted magnetic resonance imaging (MRI). We found dose-dependent changes in cage activity, social behavior, anxiety-related exploration, and spatio-cognitive performance. Although behavioral alterations in low-dose exposed animals were mild, we did unveil that both emotionality and higher cognitive abilities were affected in mice exposed to ≥0.10 Gy. Microcephaly was apparent from 0.33 Gy onwards and accompanied by deviations in regional brain volumes as compared to controls. Of note, total brain volume and the relative volume of the ventricles, frontal and posterior cerebral cortex, cerebellum, and striatum were most strongly correlated to altered behavioral parameters. Taken together, we present conclusive evidence for persistent low-dose effects after prenatal irradiation in mice and provide a better understanding of the correlation between their brain size and performance in behavioral tests.
已知产前辐射会干扰大脑发育。流行病学研究表明,孕期第8至15周接触辐射与智力残疾和小头畸形的发生率增加有关。此类神经缺陷在动物模型中也有重现,在这些模型中,啮齿动物行为测试是评估辐射诱导的大脑功能缺陷常用的工具。然而,到目前为止,动物研究表明阈值剂量约为0.30戈瑞(Gy),低于此剂量则观察不到行为改变,而人体研究暗示,接触低至0.10 Gy的剂量后会出现后期缺陷。在此,我们在胚胎第11天对怀孕小鼠进行急性辐照,剂量范围为0.10至1.00 Gy。通过一系列行为测试和容积三维T2加权磁共振成像(MRI),对子宫内辐照后大脑功能和结构改变的剂量反应关系进行了全面研究。我们发现笼内活动、社交行为、焦虑相关探索和空间认知表现存在剂量依赖性变化。虽然低剂量暴露动物的行为改变较为轻微,但我们确实发现,暴露于≥0.10 Gy的小鼠的情绪和更高认知能力均受到影响。从0.33 Gy起明显出现小头畸形,与对照组相比,同时伴有区域脑容量偏差。值得注意的是,全脑体积以及脑室、额叶和后叶皮质、小脑和纹状体的相对体积与行为参数改变的相关性最强。综上所述,我们提供了小鼠产前辐照后持续低剂量效应的确凿证据,并更好地理解了它们的脑大小与行为测试表现之间的相关性。