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MRI显示大鼠模型中早期区域性 cuprizone 诱导的脱髓鞘病变。

Early regional cuprizone-induced demyelination in a rat model revealed with MRI.

作者信息

Oakden Wendy, Bock Nicholas A, Al-Ebraheem Alia, Farquharson Michael J, Stanisz Greg J

机构信息

Physical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.

Psychology, Neuroscience and Behavior, McMaster University, Hamilton, Ontario, Canada.

出版信息

NMR Biomed. 2017 Sep;30(9). doi: 10.1002/nbm.3743. Epub 2017 May 22.

Abstract

The cuprizone model of demyelination is well established in the mouse as a tool for the study of the mechanisms of both demyelination and remyelination. It is often desirable, however, to have a larger model, such as the rat, especially for imaging-based studies, yet initial work has failed to show demyelination in cuprizone-fed rats. Several recent studies have demonstrated demyelination in the rat, but only in the corpus callosum. In this study, we acquired high-resolution, three-dimensional images of the whole brain every 2 weeks, using a T -weighted magnetization-prepared rapid acquisition gradient echo imaging sequence, optimized for myelin contrast, in order to assess myelination across the entire rat brain over a period of 8 weeks on a 1% cuprizone diet. We observed a consistent pattern of demyelination, beginning in the cerebellum by 4 weeks and involving more rostral regions of the brain by 8 weeks on the cuprizone diet, with validation using Luxol fast blue histology. This imaging technique permits the effects of cuprizone-induced demyelination to be followed longitudinally in a single animal, over the entire brain. In turn, this may facilitate the establishment of the cuprizone model of demyelination in the rat.

摘要

作为研究脱髓鞘和髓鞘再生机制的工具,铜螯合剂诱导的脱髓鞘模型在小鼠中已得到充分确立。然而,通常需要一个更大的模型,比如大鼠模型,特别是对于基于成像的研究,但最初的研究未能在喂食铜螯合剂的大鼠中显示出脱髓鞘现象。最近的几项研究已证明大鼠会出现脱髓鞘,但仅在胼胝体中。在本研究中,我们使用针对髓磷脂对比度优化的T加权磁化准备快速采集梯度回波成像序列,每2周获取一次全脑的高分辨率三维图像,以便在8周时间内评估喂食1%铜螯合剂饮食的大鼠全脑的髓鞘形成情况。我们观察到一种一致的脱髓鞘模式,在喂食铜螯合剂饮食的情况下,4周时从小脑开始,到8周时累及大脑更靠前的区域,并通过使用卢氏固蓝组织学方法进行了验证。这种成像技术能够在单个动物的整个大脑中纵向跟踪铜螯合剂诱导的脱髓鞘效应。反过来,这可能有助于在大鼠中建立铜螯合剂诱导的脱髓鞘模型。

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