Department of Anesthesiology and Pain Medicine, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Int J Mol Med. 2013 Dec;32(6):1287-92. doi: 10.3892/ijmm.2013.1504. Epub 2013 Sep 24.
The two most common forms of chronic pain are inflammatory pain and neuropathic pain. Nevertheless, the underlying mechanisms of these pain conditions and their therapeutic responses are poorly understood. MicroRNAs (miRNAs) negatively regulate cell genes, and thus control cell proliferation, inflammation and metabolism. In the present study, we examined gene expression in the hippocampus of rats in two models of chronic pain. In addition, we used the left hindpaw procedure to identify differences in the bilateral hippocampus. We divided the rats into the 4 following groups: the group with chronic constriction injury (CCI), the sham-operated group, the group injected with complete Freund's adjuvant (CFA) and the group injected with normal saline. miRNA expression profiles were analyzed using TaqMan low-density array (TLDA). We observed 54 miRNAs (22.7%) in the rats with CCI rats that were differentially expressed, including 7 miRNAs that were downregulated compared with the sham-operated rats. In the CFA-injected rats, 40 miRNAs (16.8%) were differentially expressed, including 8 miRNAs that were downregulated compared with the normal saline-injected rats. Pearson's correlation co-efficient for all detected miRNAs in the rat hippocampus failed to identify differences between the hippocampi bilaterally. An unsupervised cluster analysis produced separate clusters between the control and experimental groups. In this study, we demonstrate the differential expression of hippocampal miRNAs in two rat models of chronic pain; however, no significant differences were observed bilaterally in hippocampal miRNA expression. Further research is required to determine the correlation among miRNAs, messenger RNAs (mRNAs) and proteins.
两种最常见的慢性疼痛形式是炎症性疼痛和神经性疼痛。然而,这些疼痛状况的潜在机制及其治疗反应仍知之甚少。microRNAs(miRNAs)负向调节细胞基因,从而控制细胞增殖、炎症和代谢。在本研究中,我们在两种慢性疼痛模型中检查了大鼠海马中的基因表达。此外,我们使用左后爪程序来识别双侧海马中的差异。我们将大鼠分为以下 4 组:慢性缩窄性损伤(CCI)组、假手术组、完全弗氏佐剂(CFA)注射组和生理盐水注射组。使用 TaqMan 低密度阵列(TLDA)分析 miRNA 表达谱。我们观察到 CCI 大鼠中有 54 个 miRNA(22.7%)差异表达,其中 7 个 miRNA 与假手术组相比下调。在 CFA 注射大鼠中,有 40 个 miRNA(16.8%)差异表达,其中 8 个 miRNA 与生理盐水注射大鼠相比下调。在大鼠海马中所有检测到的 miRNA 的 Pearson 相关系数未能识别双侧海马之间的差异。无监督聚类分析在对照组和实验组之间产生了单独的聚类。在这项研究中,我们证明了两种慢性疼痛大鼠模型中海马 miRNAs 的差异表达;然而,在海马 miRNA 表达方面没有观察到双侧的显著差异。需要进一步研究以确定 miRNAs、信使 RNA(mRNAs)和蛋白质之间的相关性。