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微小RNA在神经性疼痛中的作用

The Role of miRNAs in Neuropathic Pain.

作者信息

Morchio Martina, Sher Emanuele, Collier David A, Lambert Daniel W, Boissonade Fiona M

机构信息

School of Clinical Dentistry, University of Sheffield, Sheffield S10 2TA, UK.

The Neuroscience Institute, University of Sheffield, Sheffield S10 2TN, UK.

出版信息

Biomedicines. 2023 Mar 3;11(3):775. doi: 10.3390/biomedicines11030775.

Abstract

Neuropathic pain is a debilitating condition affecting around 8% of the adult population in the UK. The pathophysiology is complex and involves a wide range of processes, including alteration of neuronal excitability and synaptic transmission, dysregulated intracellular signalling and activation of pro-inflammatory immune and glial cells. In the past 15 years, multiple miRNAs-small non-coding RNA-have emerged as regulators of neuropathic pain development. They act by binding to target mRNAs and preventing the translation into proteins. Due to their short sequence (around 22 nucleotides in length), they can have hundreds of targets and regulate several pathways. Several studies on animal models have highlighted numerous miRNAs that play a role in neuropathic pain development at various stages of the nociceptive pathways, including neuronal excitability, synaptic transmission, intracellular signalling and communication with non-neuronal cells. Studies on animal models do not always translate in the clinic; fewer studies on miRNAs have been performed involving human subjects with neuropathic pain, with differing results depending on the specific aetiology underlying neuropathic pain. Further studies using human tissue and liquid samples (serum, plasma, saliva) will help highlight miRNAs that are relevant to neuropathic pain diagnosis or treatment, as biomarkers or potential drug targets.

摘要

神经性疼痛是一种使人衰弱的病症,影响着英国约8%的成年人口。其病理生理学很复杂,涉及广泛的过程,包括神经元兴奋性和突触传递的改变、细胞内信号传导失调以及促炎性免疫细胞和神经胶质细胞的激活。在过去15年中,多种微小RNA(miRNA,即小的非编码RNA)已成为神经性疼痛发展的调节因子。它们通过与靶mRNA结合并阻止其翻译成蛋白质来发挥作用。由于其序列短(长度约为22个核苷酸),它们可以有数百个靶标并调节多种途径。多项针对动物模型的研究突出了众多在伤害感受通路不同阶段的神经性疼痛发展中起作用的miRNA,包括神经元兴奋性、突触传递、细胞内信号传导以及与非神经元细胞的通讯。动物模型研究的结果并不总是能应用于临床;针对患有神经性疼痛的人类受试者开展的miRNA研究较少,且根据神经性疼痛的具体病因不同,结果也有所差异。使用人体组织和液体样本(血清、血浆、唾液)进行的进一步研究将有助于找出与神经性疼痛诊断或治疗相关的miRNA,作为生物标志物或潜在的药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4fa/10045079/f506469732ef/biomedicines-11-00775-g001.jpg

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