Parekh Mansi B, Rutt Brian K, Purcell Ryan, Chen Yuanxin, Zeineh Michael M
Department of Radiology, Stanford University, Stanford, CA, USA.
Department of Radiology, Stanford University, Stanford, CA, USA.
Neuroimage. 2015 May 15;112:1-6. doi: 10.1016/j.neuroimage.2015.02.029. Epub 2015 Feb 19.
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 7.0T whole brain imaging sequence, balanced steady-state free precession (bSSFP) that can achieve 0.4mm 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 0.1mm 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.
海马体在记忆形成与提取以及各种神经疾病(如阿尔茨海默病、癫痫和抑郁症)中是一个非常重要的结构。它由许多错综复杂的亚区域组成,这使得研究疾病过程中发生的解剖学变化变得困难。与猴子和啮齿动物相比,人类海马体门可能具有独特的神经解剖结构,与啮齿动物相比,人类的CA3h区大大扩大,并且一种称为终叶通路的白质通路可能仅存在于人类中。在本研究中,我们使用新开发的7.0T全脑成像序列——平衡稳态自由进动(bSSFP),其能够获得各向同性为0.4mm的图像,以在活体状态下研究海马体门的解剖结构。根据解剖图谱对海马体进行详细的亚区域分割,划分以下区域:CA4、CA3、CA2、CA1、辐射层分子层(SRLM)、海马槽、穹窿以及海马下托及其分子层。我们还分割了海马体门中央的一个低信号结构,其类似于终叶通路。为了验证这种低信号代表终叶通路,我们在一个切除的标本上采集了各向同性为0.1mm的8期循环bSSFP,然后使用抗髓鞘碱性蛋白抗体(SMI 94)对标本进行切片和髓鞘染色。对髓鞘染色的切片进行结构张量分析以显示下层纤维的方向性。在所有受试者的活体海马体内均持续观察到终叶通路。它是海马体中的一条中央通路,在神经退行性疾病中的相关性未知,但既然它可以通过非侵入性方式观察到,我们就能够研究其在神经退行性变中的功能和改变。