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脊髓 microRNAs 在慢性神经性疼痛大鼠模型中的表达。

Expression of spinal cord microRNAs in a rat model of chronic neuropathic pain.

机构信息

Department of Anesthesiology, University Hospital Düsseldorf, Moorenstr.5, 40225 Düsseldorf, Germany.

出版信息

Neurosci Lett. 2012 Jan 11;506(2):281-6. doi: 10.1016/j.neulet.2011.11.023. Epub 2011 Nov 23.

Abstract

Neuropathic pain is accompanied by significant alterations of gene expression patterns in the somatosensory nervous system. The spinal cord is particularly prone to neuroplastic changes. Since the expression of microRNAs (miRNAs) has been linked to numerous pathophysiological processes, a contribution of miRNAs to the maladaptive plasticity of the spinal cord in neuropathic pain is possible. Aim of the present study therefore was to characterize the specific expression pattern of miRNAs in the rat spinal cord. Furthermore, we evaluated the time-dependent changes in expression patterns of spinal miRNAs in the chronic constriction injury (CCI) model of neuropathic pain in rats. Results from miRNA microarrays revealed a distinct expression pattern of miRNAs in the rat spinal cord. MiRNAs-494, -720, -690 and -668 showed the highest signal intensities. Members of the let-7 family as well as miR-124 belong to the group of the most highly expressed miRNAs. Induction of neuropathic pain by CCI did not lead to relevant differences in spinal miRNA expression levels compared to sham-operated animals at any studied time point. Therefore, modulation of miRNAs does not seem to contribute significantly to the changes in gene expression that cause neural plasticity in the spinal cord in this model of chronic neuropathic pain.

摘要

神经病理性疼痛伴随着躯体感觉神经系统中基因表达模式的显著改变。脊髓特别容易发生神经可塑性变化。由于 microRNAs(miRNAs)的表达与许多病理生理过程有关,miRNAs 可能对神经病理性疼痛脊髓的适应性可塑性变化有贡献。因此,本研究的目的是描述大鼠脊髓中 miRNAs 的特定表达模式。此外,我们评估了在慢性压迫性损伤(CCI)神经病理性疼痛大鼠模型中脊髓 miRNAs 表达模式的时间依赖性变化。miRNA 微阵列的结果显示大鼠脊髓中存在独特的 miRNAs 表达模式。miRNAs-494、-720、-690 和 -668 表现出最高的信号强度。let-7 家族成员和 miR-124 属于表达最高的 miRNAs 之一。与 sham 手术组相比,CCI 诱导的神经病理性疼痛在任何研究时间点均未导致脊髓 miRNA 表达水平的相关差异。因此,在这种慢性神经病理性疼痛模型中,miRNAs 的调节似乎对导致脊髓神经可塑性的基因表达变化没有显著贡献。

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