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首页> 外文期刊>NeuroImage >Ultra-high resolution in-vivo 7.0 T structural imaging of the human hippocampus reveals the endfolial pathway
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Ultra-high resolution in-vivo 7.0 T structural imaging of the human hippocampus reveals the endfolial pathway

机译:海马的超高分辨率体内7.0 T结构成像揭示了叶端途径

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摘要

The hippocampus is a very important structure in memory formation and retrieval, as well as in various neurological disorders such as Alzheimer's disease, epilepsy and depression. It is composed of many intricate subregions making it difficult to study the anatomical changes that take place during disease. The hippocampal hilus may have a unique neuroanatomy in humans compared to that in monkeys and rodents, with field CA3h greatly enlarged in humans compared to that in rodents, and a white-matter pathway, called the endfolial pathway, possibly only present in humans. In this study we have used newly developed 7.0 T whole brain imaging sequence, balanced steady-state free precession (bSSFP) that can achieve 0.4 mm isotropic images to study, in vivo, the anatomy of the hippocampal hilus. A detailed hippocampal subregional segmentation was performed according to anatomic atlases segmenting the following regions: CA4, CA3, CA2, CA1, SRLM (stratum radiatum lacunosum moleculare), alveus, fornix, and subiculum along with its molecular layer. We also segmented a hypointense structure centrally within the hilus that resembled the endfolial pathway. To validate that this hypointense signal represented the endfolial pathway, we acquired 0.1 mm isotropic 8-phase cycle bSSFP on an excised specimen, and then sectioned and stained the specimen for myelin using an anti-myelin basic protein antibody (SMI 94). A structure tensor analysis was calculated on the myelin-stained section to show directionality of the underlying fibers. The endfolial pathway was consistently visualized within the hippocampal body in vivo in all subjects. It is a central pathway in the hippocampus, with unknown relevance in neurodegenerative disorders, but now that it can be visualized noninvasively, we can study its function and alterations in neurodegeneration. (C) 2015 Elsevier Inc. All rights reserved.
机译:海马是记忆形成和恢复以及各种神经系统疾病(例如阿尔茨海默氏病,癫痫和抑郁症)中非常重要的结构。它由许多复杂的子区域组成,因此很难研究疾病期间发生的解剖学变化。与猴子和啮齿类动物相比,海马体在人类中可能具有独特的神经解剖结构,与啮齿类动物相比,人类的视野CA3h大大扩大,并且白质途径(称为叶端途径)可能仅在人类中存在。在这项研究中,我们使用了新开发的7.0 T全脑成像序列,可以实现0.4 mm各向同性图像的平衡稳态自由进动(bSSFP),以在体内研究海马hilus的解剖结构。根据解剖图谱对以下区域进行了详细的海马亚区域分割:CA4,CA3,CA2,CA1,SPALM(层状放射状分子),肺泡,穹ni和下丘以及其分子层。我们还在与叶端途径相似的hilus中央段分割了一个低位结构。为了验证该低信号代表了叶端途径,我们在切除的标本上获得了0.1 mm各向同性的8相周期bSSFP,然后使用抗髓磷脂碱性蛋白抗体(SMI 94)对标本进行切片和染色。在髓磷脂染色的截面上计算结构张量分析,以显示下层纤维的方向性。在所有受试者体内,在海马体内均持续观察到了叶端途径。它是海马中枢的一条通路,与神经退行性疾病的相关性未知,但是现在可以无创地观察到它,我们可以研究其在神经变性中的功能和改变。 (C)2015 Elsevier Inc.保留所有权利。

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