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产前脑缺血通过干扰神经元树突分支破坏 MRI 定义的皮质微观结构。

Prenatal cerebral ischemia disrupts MRI-defined cortical microstructure through disturbances in neuronal arborization.

机构信息

Department of Pediatrics, Oregon Health & Science University, Portland, OR 97239, USA.

Advanced Imaging Research Center, Oregon Health & Science University, Portland, OR 97239, USA.

出版信息

Sci Transl Med. 2013 Jan 16;5(168):168ra7. doi: 10.1126/scitranslmed.3004669.

Abstract

Children who survive preterm birth exhibit persistent unexplained disturbances in cerebral cortical growth with associated cognitive and learning disabilities. The mechanisms underlying these deficits remain elusive. We used ex vivo diffusion magnetic resonance imaging to demonstrate in a preterm large-animal model that cerebral ischemia impairs cortical growth and the normal maturational decline in cortical fractional anisotropy (FA). Analysis of pyramidal neurons revealed that cortical deficits were associated with impaired expansion of the dendritic arbor and reduced synaptic density. Together, these findings suggest a link between abnormal cortical FA and disturbances of neuronal morphological development. To experimentally investigate this possibility, we measured the orientation distribution of dendritic branches and observed that it corresponds with the theoretically predicted pattern of increased anisotropy within cases that exhibited elevated cortical FA after ischemia. We conclude that cortical growth impairments are associated with diffuse disturbances in the dendritic arbor and synapse formation of cortical neurons, which may underlie the cognitive and learning disabilities in survivors of preterm birth. Further, measurement of cortical FA may be useful for noninvasively detecting neurological disorders affecting cortical development.

摘要

早产儿存活后会出现持续性的、无法解释的大脑皮质生长紊乱,并伴有认知和学习障碍。这些缺陷的发生机制仍不清楚。我们使用离体弥散磁共振成像,在早产大动物模型中证明,脑缺血会损害皮质生长,并使皮质分数各向异性(FA)正常成熟过程中下降。对锥体神经元的分析表明,皮质缺陷与树突分支的扩张受损和突触密度降低有关。这些发现表明,异常的皮质 FA 与神经元形态发育的紊乱之间存在联系。为了在实验上研究这种可能性,我们测量了树突分支的取向分布,发现其与理论上预测的模式相吻合,即在缺血后皮质 FA 升高的病例中,增加了各向异性。我们得出结论,皮质生长受损与皮质神经元树突和突触形成的弥漫性紊乱有关,这可能是早产儿存活后认知和学习障碍的基础。此外,皮质 FA 的测量可能有助于非侵入性地检测影响皮质发育的神经发育障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f2f/3857141/fc4fbb70cb0b/nihms-529295-f0001.jpg

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