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

机译:脊髓微RNA在慢性神经性疼痛大鼠模型中的表达

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摘要

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.
机译:神经性疼痛伴随着体感神经系统中基因表达模式的显着改变。脊髓特别容易发生神经塑性变化。由于microRNA(miRNA)的表达与许多病理生理过程有关,因此miRNA对神经性疼痛中脊髓适应不良的可塑性的贡献是可能的。因此,本研究的目的是表征大鼠脊髓中miRNA的特异性表达模式。此外,我们评估了大鼠神经性疼痛的慢性收缩损伤(CCI)模型中脊髓miRNA表达模式的时间依赖性变化。 miRNA微阵列的结果显示了大鼠脊髓中miRNA的独特表达模式。 MiRNA-494,-720,-690和-668显示出最高的信号强度。 let-7家族的成员以及miR-124都属于表达水平最高的miRNA。与假手术动物相比,在任何研究的时间点,CCI诱导的神经性疼痛均未导致脊髓miRNA表达水平的相关差异。因此,在这种慢性神经性疼痛模型中,miRNA的调节似乎不会对导致脊髓神经可塑性的基因表达变化产生重大影响。

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