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Cerebellar Pathways in Mouse Model of Purkinje Cell Degeneration Detected by High-Angular Resolution Diffusion Imaging Tractography

机译:高角度分辨率扩散成像术检测到的浦肯野细胞变性小鼠模型中的小脑通路。

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摘要

Cerebellar MR imaging has several challenging aspects, due to the fine, repetitive layered structure of cortical folia with underlying axonal pathways. In this MR study, we imaged with high-angular resolution diffusion imaging (HARDI) abnormal cerebellar cortical structure (gray matter) and myelinated axonal pathways (white matter) of a mouse spontaneous mutation, Purkinje cell degeneration (pcd), in which almost all Purkinje neurons degenerate, mainly between postnatal days 20 and 35. Mouse brains at postnatal day 20 (P20) and at 8 months were scanned, and known or expected abnormalities, such as reduction of the white matter volume, disorganized pathways likely linked to parallel fibers, mossy fibers, and other fibers running from/to the cerebellar cortex were observed in mutant mice. Such abnormalities were detected at both an early and a fully advanced degeneration stage. These results suggest that our diffusion MR tractography is useful for early detection and tracking of neuropathology in the cerebellum.
机译:小脑MR成像具有许多挑战性的方面,这是由于皮质叶的精细,重复的分层结构以及潜在的轴突途径。在这项MR研究中,我们使用了小鼠自发突变浦肯野细胞变性(pcd)的高角度分辨率扩散成像(HARDI)小脑皮质结构异常(灰质)和髓鞘轴突途径(白质)进行了成像浦肯野神经元退化,主要在出生后第20至35天之间。扫描小鼠的大脑在出生后第20天(P20)和第8个月,发现或预期异常,例如白质体积减少,可能与平行纤维相关的途径混乱在突变小鼠中观察到了来自小脑皮层的苔藓纤维,苔藓纤维和其他纤维。在早期和完全晚期变性阶段均检测到此类异常。这些结果表明,我们的弥散MR描记法可用于早期检测和跟踪小脑的神经病理学。

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