Tovar-Moll Fernanda, Moll Jorge, de Oliveira-Souza Ricardo, Bramati Ivanei, Andreiuolo Pedro A, Lent Roberto
Department of Anatomy, Institute of Biomedical Sciences, Federal University of Rio de Janeiro, Brazil.
Cereb Cortex. 2007 Mar;17(3):531-41. doi: 10.1093/cercor/bhj178. Epub 2006 Apr 20.
Callosal dysgenesis (CD) is observed in many neurodevelopmental conditions, but its subjacent mechanisms are unknown, despite extensive research on animals. Here we employ magnetic resonance diffusion tensor imaging and tractography in human CD to reveal the aberrant circuitry of these brains. We searched particularly for evidence of plasticity. Four main findings are described--1) in the presence of a callosal remnant or a hypoplastic corpus callosum (CC), fibers therein largely connect the expected neocortical regions; 2) callosal remnants and hypoplastic CCs display a fiber topography similar to normal; 3) at least 2 long abnormal tracts are formed in patients with defective CC: the well-known Probst bundle (PB) and a so far unknown sigmoid, asymmetrical aberrant bundle connecting the frontal lobe with the contralateral occipitoparietal cortex; and 4) whereas the PB is topographically organized and has an ipsilateral U-connectivity, the sigmoid bundle is a long, heterotopic commissural tract. These observations suggest that when the developing human brain is confronted with factors that hamper CC fibers to cross the midline, some properties of the miswired fibers are maintained (such as side-by-side topography), whereas others are dramatically changed, leading to the formation of grossly abnormal white matter tracts.
胼胝体发育不全(CD)在许多神经发育疾病中都有观察到,但其潜在机制尚不清楚,尽管对动物进行了广泛研究。在此,我们利用磁共振扩散张量成像和纤维束成像技术研究人类CD患者,以揭示这些大脑的异常神经回路。我们特别寻找可塑性的证据。本文描述了四个主要发现:1)在存在胼胝体残余或胼胝体发育不全(CC)的情况下,其中的纤维主要连接预期的新皮质区域;2)胼胝体残余和发育不全的CC显示出与正常相似的纤维拓扑结构;3)在CC缺陷的患者中至少形成了2条长的异常纤维束:著名的普罗布斯特束(PB)和一条迄今为止未知的、连接额叶与对侧枕顶叶皮质的乙状、不对称异常纤维束;4)虽然PB在拓扑上有组织且具有同侧U形连接,但乙状纤维束是一条长的、异位的连合纤维束。这些观察结果表明,当发育中的人类大脑遇到阻碍CC纤维穿过中线的因素时,错误连接的纤维的一些特性得以保留(如并排拓扑结构),而其他特性则发生了巨大变化,导致形成明显异常的白质纤维束。