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小脑绒球在前庭代偿过程中的蛋白质组学分析。

Proteomic analysis of the rat cerebellar flocculus during vestibular compensation.

机构信息

Clinical Proteomics & Molecular Medicine, St. Marianna University Graduate School of Medicine, Kawasaki, Kanagawa, Japan.

出版信息

J Vestib Res. 2009;19(3-4):83-94. doi: 10.3233/VES-2009-0356.

Abstract

Unilateral labyrinthectomy (UL) in rats is used as a human vertigo model. In this model, spontaneous nystagmus and dysequilibrium caused by UL are ameliorated within 48-72 hours. The amelioration, termed vestibular compensation (VC), is long lasting. Although cerebellar flocculi have been reported to be involved in VC, the molecular mechanisms behind VC are unknown. In this study, we used 2D-DIGE to detect protein changes in flocculi during acute (48 hours) and chronic (1 week) stages of VC. We found 99 out of 967 protein spots that showed significant changes in their intensities. Of the 99 spots, 45 spots (ipsilateral side, 15; contralateral side, 30) changed unilaterally during the acute stage, whereas 46 spots (ipsilateral side, 21; contralateral side, 25) changed unilaterally during the chronic stage. Thus, the acute compensation mechanism is more complicated in the contralateral flocculus than in the ipsilateral flocculus. Using MALDI-TOF MS, we identified 10 proteins out of the 12 protein spots. Of these, 3 proteins involved in synaptic transmission, neuronal filament formation and vesicular transport, respectively, demonstrated altered expression only in the acute stage. Our results enhance the understanding of the role of the cerebellar flocculi in VC generation.

摘要

单侧迷路切除术(UL)在大鼠中被用作人类眩晕模型。在该模型中,UL 引起的自发性眼球震颤和平衡障碍会在 48-72 小时内得到改善。这种改善被称为前庭代偿(VC),且持续时间很长。尽管小脑绒球已被报道参与 VC,但 VC 的分子机制尚不清楚。在这项研究中,我们使用 2D-DIGE 来检测 VC 的急性(48 小时)和慢性(1 周)阶段绒球中的蛋白质变化。我们发现了 967 个蛋白点中有 99 个在其强度上发生了显著变化。在 99 个斑点中,有 45 个斑点(同侧,15 个;对侧,30 个)在急性阶段单侧变化,而 46 个斑点(同侧,21 个;对侧,25 个)在慢性阶段单侧变化。因此,与同侧绒球相比,急性补偿机制在对侧绒球中更为复杂。使用 MALDI-TOF MS,我们从 12 个蛋白斑点中鉴定出 10 个蛋白。其中,涉及突触传递、神经元丝形成和囊泡运输的 3 种蛋白质仅在急性阶段表现出改变的表达。我们的研究结果增强了对小脑绒球在 VC 产生中的作用的理解。

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