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通过高角分辨率扩散成像纤维束成像检测浦肯野细胞变性小鼠模型中的小脑通路。

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

作者信息

Kanamaru Yuri, Li Jianxue, Stewart Natalie, Sidman Richard L, Takahashi Emi

机构信息

Department of Medicine, Chiba University School of Medicine, Chiba, Japan.

Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

出版信息

Cerebellum. 2017 Jun;16(3):648-655. doi: 10.1007/s12311-016-0842-5.

Abstract

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.

摘要

由于小脑皮质小叶精细、重复的分层结构以及其下的轴突通路,小脑磁共振成像存在几个具有挑战性的方面。在这项磁共振研究中,我们使用高角分辨率扩散成像(HARDI)对一种小鼠自发突变体——浦肯野细胞变性(pcd)的异常小脑皮质结构(灰质)和有髓鞘轴突通路(白质)进行成像,在该突变体中,几乎所有浦肯野神经元都会退化,主要发生在出生后第20天至35天之间。对出生后第20天(P20)和8个月大的小鼠大脑进行扫描,在突变小鼠中观察到了已知或预期的异常情况,如白质体积减少、可能与平行纤维、苔藓纤维以及其他进出小脑皮质的纤维相关的通路紊乱。在早期和完全进展性退化阶段均检测到了此类异常。这些结果表明,我们的扩散磁共振纤维束成像对于小脑神经病理学的早期检测和追踪是有用的。

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Asymmetry of White Matter Pathways in Developing Human Brains.发育中人类大脑白质通路的不对称性。
Cereb Cortex. 2015 Sep;25(9):2883-93. doi: 10.1093/cercor/bhu084. Epub 2014 May 8.

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