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脊髓背角星形胶质细胞在神经病理性疼痛大鼠模型中的结构重排。

Structural reorganization of medullary dorsal horn astrocytes in a rat model of neuropathic pain.

机构信息

Department of Anatomy, Physiology and Neurobiology, School of Dentistry, Kyungpook National University, Daegu, Republic of Korea.

Brain Science & Engineering Institute, Kyungpook National University, Daegu, Republic of Korea.

出版信息

Brain Struct Funct. 2024 Sep;229(7):1757-1768. doi: 10.1007/s00429-024-02835-y. Epub 2024 Jul 25.

DOI:10.1007/s00429-024-02835-y
PMID:39052094
Abstract

Multiple studies have shown that astrocytes in the medullary dorsal horn (MDH) play an important role in the development of pathologic pain. However, little is known about the structural reorganization of the peripheral astrocytic processes (PAP), the main functional part of the astrocyte, in MDH in neuropathic state. For this, we investigated the structural relationship between PAP and their adjacent presynaptic axon terminals and postsynaptic dendrites in the superficial laminae of the MDH using electron microscopical immunohistochemistry for ezrin, a marker for PAP, and quantitative analysis in a rat model of neuropathic pain following chronic constriction injury of the infraorbital nerve (CCI-ION). We found that, compared to controls, in rats with CCI-ION, (1) the number, % area, surface density, and volume fraction of ezrin-positive (+) PAP, as well as the fraction of synaptic edge apposed by ezrin + PAP and the degree of its coverage of presynaptic axon terminals and postsynaptic dendrites increased significantly, (2) these effects were abolished by administration of the mGluR5 antagonist 2-methyl-6-(phenylethynyl) pyridine (MPEP). These findings indicate that PAP undergoes structural reorganization around the central synapses of sensory afferents following nerve injury, suggest that it may be mediated by mGluR5, and may represent the structural basis for enhancing astrocyte-neuron interaction in neuropathic pain.

摘要

多项研究表明,背角(MDH)中的星形胶质细胞在病理性疼痛的发展中起着重要作用。然而,对于在神经病理性状态下 MDH 中周围星形胶质细胞突起(PAP)的结构重排,即星形胶质细胞的主要功能部分,知之甚少。为此,我们使用针对 PAP 的标志物 ezrin 进行电子显微镜免疫组织化学,研究了 PAP 与其相邻的突触前轴突末梢和 MDH 浅层中的突触后树突之间的结构关系,并在眶下神经慢性缩窄性损伤(CCI-ION)后的神经病理性疼痛大鼠模型中进行了定量分析。我们发现,与对照组相比,CCI-ION 大鼠中,(1)ezrin 阳性(+)PAP 的数量、%面积、表面密度和体积分数,以及 ezrin+PAP 与突触边缘吻合的分数和其对突触前轴突末梢和突触后树突的覆盖程度显著增加;(2)这些效应被代谢型谷氨酸受体 5 拮抗剂 2-甲基-6-(苯乙炔基)吡啶(MPEP)所消除。这些发现表明,PAP 在神经损伤后围绕感觉传入的中枢突触发生结构重排,提示其可能由 mGluR5 介导,可能代表增强神经病理性疼痛中星形胶质细胞-神经元相互作用的结构基础。

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本文引用的文献

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脊髓疼痛处理中突触前 N-甲基-D-天冬氨酸受体理解方面的进展与障碍
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