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利用锰增强 MRI 和弥散张量成像技术在早期产后发育和可塑性中评估视网膜和胼胝体投射。

In vivo evaluation of retinal and callosal projections in early postnatal development and plasticity using manganese-enhanced MRI and diffusion tensor imaging.

机构信息

Laboratory of Biomedical Imaging and Signal Processing, Department of Electrical and Electronic Engineering, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

出版信息

Neuroimage. 2012 Feb 1;59(3):2274-83. doi: 10.1016/j.neuroimage.2011.09.055. Epub 2011 Oct 1.

Abstract

The rodents are an excellent model for understanding the development and plasticity of the visual system. In this study, we explored the feasibility of Mn-enhanced MRI (MEMRI) and diffusion tensor imaging (DTI) at 7 T for in vivo and longitudinal assessments of the retinal and callosal pathways in normal neonatal rodent brains and after early postnatal visual impairments. Along the retinal pathways, unilateral intravitreal Mn2+ injection resulted in Mn2+ uptake and transport in normal neonatal visual brains at postnatal days (P) 1, 5 and 10 with faster Mn2+ clearance than the adult brains at P60. The reorganization of retinocollicular projections was also detected by significant Mn2+ enhancement by 2%-10% in the ipsilateral superior colliculus (SC) of normal neonatal rats, normal adult mice and adult rats after neonatal monocular enucleation (ME) but not in normal adult rats or adult rats after monocular deprivation (MD). DTI showed a significantly higher fractional anisotropy (FA) by 21% in the optic nerve projected from the remaining eye of ME rats compared to normal rats at 6 weeks old, likely as a result of the retention of axons from the ipsilaterally uncrossed retinal ganglion cells, whereas the anterior and posterior retinal pathways projected from the enucleated or deprived eyes possessed lower FA after neonatal binocular enucleation (BE), ME and MD by 22%-56%, 18%-46% and 11%-15% respectively compared to normal rats, indicative of neurodegeneration or immaturity of white matter tracts. Along the visual callosal pathways, intracortical Mn2+ injection to the visual cortex of BE rats enhanced a larger projection volume by about 74% in the V1/V2 transition zone of the contralateral hemisphere compared to normal rats, without apparent DTI parametric changes in the splenium of corpus callosum. This suggested an adaptive change in interhemispheric connections and spatial specificity in the visual cortex upon early blindness. The results of this study may help determine the mechanisms of axonal uptake and transport, microstructural reorganization and functional activities in the living visual brains during development, diseases, plasticity and early interventions in a global and longitudinal setting.

摘要

啮齿动物是研究视觉系统发育和可塑性的理想模型。本研究采用 7T 下的 Mn 增强磁共振成像(MEMRI)和弥散张量成像(DTI)技术,对正常新生鼠和早期视觉损伤后视网膜和胼胝体通路进行活体和纵向评估。在视网膜通路上,单侧玻璃体内注射 Mn2+可在新生鼠 P1、P5 和 P10 时在正常新生鼠的视觉脑中摄取和转运 Mn2+,其 Mn2+清除速度快于 P60 时的成年鼠。在正常新生大鼠、成年正常小鼠和成年单侧眼摘除(ME)大鼠的同侧上丘(SC)中,也检测到视束投射的重组,表现为 Mn2+显著增强 2%-10%,但在正常成年大鼠或单侧剥夺(MD)大鼠中未检测到。DTI 显示,ME 大鼠对侧眼视神经投射的分数各向异性(FA)显著增加 21%,与正常大鼠相比,这可能是由于保留了同侧未交叉的视网膜神经节细胞的轴突,而从摘除或剥夺眼投射的前、后视网膜通路的 FA 分别降低了 22%-56%、18%-46%和 11%-15%,与正常大鼠相比,提示神经退行性变或白质束不成熟。在视交叉通路上,将 Mn2+注入 BE 大鼠的视皮层,可使对侧半球 V1/V2 过渡区的投射体积增加约 74%,而胼胝体压部的 DTI 参数无明显变化。这表明早期失明后,大脑半球间连接的适应性改变和视皮层的空间特异性。本研究结果可能有助于确定活体视觉脑中轴突摄取和转运、微结构重组以及发育、疾病、可塑性和早期干预过程中的功能活动的机制。

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