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基于体素的形态学测量和组织学分析在中风后中枢性疼痛猴模型中揭示的皮质灰质结构可塑性变化

Structural Plastic Changes of Cortical Gray Matter Revealed by Voxel-Based Morphometry and Histological Analyses in a Monkey Model of Central Post-Stroke Pain.

作者信息

Nagasaka Kazuaki, Nemoto Kiyotaka, Takashima Ichiro, Bando Daigo, Matsuda Keiji, Higo Noriyuki

机构信息

Human Informatics and Interaction Research Institute, National Institute of Advanced Industrial Science and Technology, Ibaraki 305-8568, Japan.

Institute for Human Movement and Medical Science, Niigata University of Health and Welfare, Niigata 950-3198, Japan.

出版信息

Cereb Cortex. 2021 Aug 26;31(10):4439-4449. doi: 10.1093/cercor/bhab098.

Abstract

Central post-stroke pain (CPSP) is a chronic pain caused by stroke lesions of somatosensory pathways. Several brain imaging studies among patients with CPSP demonstrate that the pathophysiological mechanism underlying this condition is the maladaptive plasticity of pain-related brain regions. However, the temporal profile of the regional plastic changes, as suggested by brain imaging of CPSP patients, as well as their cellular basis, is unknown. To investigate these issues, we performed voxel-based morphometry (VBM) using T1-weighted magnetic resonance imaging and immunohistochemical analysis with our established CPSP monkey model. From 8 weeks after a hemorrhagic lesion to the unilateral ventral posterolateral nucleus of the thalamus, the monkeys exhibited significant behavioral changes that were interpreted as reflecting allodynia. The present VBM results revealed a decrease in gray matter volume in the pain-related areas after several weeks following the lesion. Furthermore, immunohistochemical staining in the ipsilesional posterior insular cortex (ipsi-PIC) and secondary somatosensory cortex (ipsi-SII), where the significant reduction in gray matter volume was observed in the VBM result, displayed a significant reduction in both excitatory and inhibitory synaptic terminals compared to intact monkeys. Our results suggest that progressive changes in neuronal morphology, including synaptic loss in the ipsi-PIC/SII, are involved in theCPSP.

摘要

中风后中枢性疼痛(CPSP)是一种由体感通路中风损伤引起的慢性疼痛。对CPSP患者进行的多项脑成像研究表明,这种疾病的病理生理机制是疼痛相关脑区的适应性不良可塑性。然而,CPSP患者脑成像所显示的区域可塑性变化的时间特征及其细胞基础尚不清楚。为了研究这些问题,我们使用T1加权磁共振成像进行基于体素的形态测量(VBM),并对我们建立的CPSP猴子模型进行免疫组织化学分析。从丘脑单侧腹后外侧核出血性损伤后8周起,猴子表现出明显的行为变化,这些变化被解释为反映了异常性疼痛。目前的VBM结果显示,损伤后数周,疼痛相关区域的灰质体积减少。此外,在VBM结果中观察到灰质体积显著减少的患侧后岛叶皮质(ipsi-PIC)和次级体感皮质(ipsi-SII)进行免疫组织化学染色,与完整猴子相比,兴奋性和抑制性突触终末均显著减少。我们的结果表明,神经元形态的渐进性变化,包括ipsi-PIC/SII中的突触丧失,与CPSP有关。

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