Center for Biomedical Imaging, Department of Radiology, New York University School of Medicine, New York, NY 10016, USA.
NMR Biomed. 2010 Aug;23(7):711-24. doi: 10.1002/nbm.1577.
Multisite exchange models have been applied frequently to quantify measurements of transverse relaxation and diffusion in living tissues. Although the simplicity of such models is attractive, the precise relationship of the model parameters to tissue properties may be difficult to ascertain. Here, we investigate numerically a two-compartment exchange (Kärger) model as applied to diffusion in a system of randomly packed identical parallel cylinders with permeable walls, representing cells with permeable membranes, that may serve particularly as a model for axons in the white matter of the brain. By performing Monte Carlo simulations of restricted diffusion, we show that the Kärger model may provide a reasonable coarse-grained description of the diffusion-weighted signal in the long time limit, as long as the cell membranes are sufficiently impermeable, i.e. whenever the residence time in a cell is much longer than the time it takes to diffuse across it. For larger permeabilities, the exchange time obtained from fitting to the Kärger model overestimates the actual exchange time, leading to an underestimated value of cell membrane permeability.
多站点交换模型常用于量化活体组织中横向弛豫和扩散的测量。尽管此类模型具有吸引力,但要确定模型参数与组织特性的确切关系可能具有一定难度。在这里,我们对应用于具有可渗透壁的随机堆积相同平行圆柱系统中的扩散的两室交换(Kärger)模型进行了数值研究,该模型代表具有可渗透膜的细胞,可特别作为脑白质中轴突的模型。通过对受限扩散进行蒙特卡罗模拟,我们表明,只要细胞膜足够不渗透,即只要细胞内的停留时间远长于穿过细胞膜所需的时间,Kärger 模型就可以在长时间限制内为扩散加权信号提供合理的粗粒度描述。对于更大的渗透率,从 Kärger 模型拟合得到的交换时间会高估实际的交换时间,从而导致细胞膜渗透率的低估。