Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, The Netherlands.
Empenn, INRIA, INSERM, CNRS, Université de Rennes 1, Rennes, France.
Magn Reson Med. 2022 Jul;88(1):380-390. doi: 10.1002/mrm.29213. Epub 2022 Mar 28.
Ex vivo imaging is a commonly used approach to investigate the biophysical mechanism of orientation-dependent signal phase evolution in white matter. Yet, how phase measurements are influenced by the structural alteration in the tissue after formalin fixation is not fully understood. Here, we study the effects on magnetic susceptibility, microstructural compartmentalization, and chemical exchange measurement with a postmortem formalin-fixed whole-brain human tissue.
A formalin-fixed, postmortem human brain specimen was scanned with multiple orientations to the main magnetic field direction for robust bulk magnetic susceptibility measurement with conventional quantitative susceptibility imaging models. White matter samples were subsequently excised from the whole-brain specimen and scanned in multiple rotations on an MRI scanner to measure the anisotropic magnetic susceptibility and microstructure-related contributions in the signal phase and to validate the findings of the whole-brain data.
The bulk isotropic magnetic susceptibility of ex vivo whole-brain imaging is comparable to in vivo imaging, with noticeable enhanced nonsusceptibility contributions. The excised specimen experiment reveals that anisotropic magnetic susceptibility and compartmentalization phase effect were considerably reduced in the formalin-fixed white matter specimens.
Formalin-fixed postmortem white matter exhibits comparable isotropic magnetic susceptibility to previous in vivo imaging findings. However, the measured phase and magnitude data of the fixed white matter tissue shows a significantly weaker orientation dependency and compartmentalization effect. Alternatives to formalin fixation are needed to better reproduce the in vivo microstructural effects in postmortem samples.
在体成像常用于研究白质中与方向相关的信号相位演化的生物物理机制。然而,福尔马林固定后组织结构改变如何影响相位测量尚不完全清楚。在此,我们研究了福尔马林固定的全脑人脑组织的磁导率、微结构分隔和化学交换测量的影响。
对福尔马林固定的死后人脑标本进行多方向扫描,以常规定量磁敏感成像模型进行稳健的体各向异性磁导率测量。随后从全脑标本中取出白质样本,并在 MRI 扫描仪上进行多次旋转扫描,以测量信号相位中的各向异性磁导率和与微结构相关的贡献,并验证全脑数据的结果。
离体全脑成像的各向同性体磁导率与体内成像相当,具有明显增强的非磁导率贡献。离体标本实验表明,福尔马林固定的白质标本中的各向异性磁导率和分隔相位效应显著降低。
福尔马林固定的死后白质表现出与以前的体内成像发现相当的各向同性磁导率。然而,固定白质组织的测量相位和幅度数据显示出明显较弱的方向依赖性和分隔效应。需要替代福尔马林固定以更好地在死后样本中重现体内微观结构效应。