Department of Neurobiology, Yale University School of Medicine, New Haven, CT 06511-6624, USA.
Brain Struct Funct. 2012 Apr;217(2):459-72. doi: 10.1007/s00429-011-0350-9. Epub 2011 Oct 8.
Using a novel mouse model of early life neglect and abuse (ENA) based on maternal separation with early weaning, George et al. (BMC Neurosci 11:123, 2010) demonstrated behavioral abnormalities in adult mice, and Bordner et al. (Front Psychiatry 2(18):1-18, 2011) described concomitant changes in mRNA and protein expression. Using the same model, here we report neuroanatomical changes that include smaller brain size and abnormal inter-hemispheric asymmetry, decreases in cortical thickness, abnormalities in subcortical structures, and white matter disorganization and atrophy most severely affecting the left hemisphere. Because of the similarities between the neuroanatomical changes observed in our mouse model and those described in human survivors of ENA, this novel animal model is potentially useful for studies of human ENA too costly or cumbersome to be carried out in primates. Moreover, our current knowledge of the mouse genome makes this model particularly suited for targeted anatomical, molecular, and pharmacological experimentation not yet possible in other species.
利用一种新的基于母婴分离和早期断奶的幼年忽视和虐待(ENA)小鼠模型,George 等人(BMC Neurosci 11:123, 2010)证明了成年小鼠存在行为异常,Bordner 等人(Front Psychiatry 2(18):1-18, 2011)则描述了伴随的 mRNA 和蛋白质表达变化。在这里,我们使用相同的模型报告了神经解剖学变化,包括大脑体积减小和半球间不对称异常、皮质厚度减少、皮质下结构异常以及白质紊乱和萎缩,其中左侧半球受影响最严重。由于我们的小鼠模型中观察到的神经解剖学变化与 ENA 幸存者中描述的变化相似,因此这种新型动物模型对于人类 ENA 的研究可能是有用的,因为在灵长类动物中进行这些研究过于昂贵或复杂。此外,我们目前对小鼠基因组的了解使得这种模型特别适合于靶向解剖学、分子和药理学实验,而在其他物种中尚无法进行这些实验。