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非编码RNA在神经性疼痛方面的研究进展

Advances With Non-coding RNAs in Neuropathic Pain.

作者信息

Hu Cheng, He Menglin, Xu Qian, Tian Weiqian

机构信息

Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, China.

出版信息

Front Neurosci. 2021 Dec 23;15:760936. doi: 10.3389/fnins.2021.760936. eCollection 2021.


DOI:10.3389/fnins.2021.760936
PMID:35002601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8733285/
Abstract

Neuropathic pain (NP) is one of the most common types of clinical pain. The common causes of this syndrome include injury to the central or peripheral nervous systems and pathological changes. NP is characterized by spontaneous pain, hyperalgesia, abnormal pain, and paresthesia. Because of its diverse etiology, the pathogenesis of NP has not been fully elucidated and has become one of the most challenging problems in clinical medicine. This kind of pain is extremely resistant to conventional treatment and is accompanied by serious complications. Non-coding RNAs (ncRNAs), such as microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), contribute to diverse biological processes by regulating the expression of various mRNAs involved in pain-related pathways, at the posttranscriptional level. Abnormal regulation of ncRNAs is closely related to the occurrence and development of NP. In this review, we summarize the current state of understanding of the roles of different ncRNAs in the development of NP. Understanding these mechanisms can help develop novel therapeutic strategies to prevent or treat chronic pain.

摘要

神经病理性疼痛(NP)是临床疼痛中最常见的类型之一。该综合征的常见病因包括中枢或外周神经系统损伤以及病理变化。NP的特征是自发性疼痛、痛觉过敏、异常疼痛和感觉异常。由于其病因多样,NP的发病机制尚未完全阐明,已成为临床医学中最具挑战性的问题之一。这种疼痛对传统治疗极具抗性,并伴有严重并发症。非编码RNA(ncRNAs),如微小RNA(miRNAs)、长链非编码RNA(lncRNAs)和环状RNA(circRNAs),通过在转录后水平调节参与疼痛相关途径的各种mRNA的表达,参与多种生物学过程。ncRNAs的异常调节与NP的发生和发展密切相关。在本综述中,我们总结了目前对不同ncRNAs在NP发生发展中作用的理解现状。了解这些机制有助于开发预防或治疗慢性疼痛的新治疗策略。

相似文献

[1]
Advances With Non-coding RNAs in Neuropathic Pain.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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引用本文的文献

[1]
The involvement of spinal lncRNA RT1-CE10 in chronic functional visceral pain.

Mol Pain. 2025

[2]
The analgesic mechanism of electroacupuncture at the central level for neuropathic pain: a review of studies based on animal experiments.

Front Neurol. 2025-5-29

[3]
Transcriptome Analysis of Non-coding RNAs and mRNAs in the Dorsal Root Ganglion of Peripheral Nerve Injury-Induced Neuropathic Pain.

Biochem Genet. 2025-2-24

[4]
RNA Interference Unleashed: Current Perspective of Small Interfering RNA (siRNA) Therapeutics in the Treatment of Neuropathic Pain.

ACS Pharmacol Transl Sci. 2024-9-23

[5]
Therapeutic Implication of miRNAs as an Active Regulatory Player in the Management of Pain: A Review.

Genes (Basel). 2024-7-31

[6]
Communicating pain: emerging axonal signaling in peripheral neuropathic pain.

Front Neuroanat. 2024-7-9

[7]
Pharmacogenetic landscape of pain management variants among Mediterranean populations.

Front Pharmacol. 2024-5-15

[8]
Recent Advances in Management of Neuropathic, Nociceptive, and Chronic Pain: A Narrative Review with Focus on Nanomedicine, Gene Therapy, Stem Cell Therapy, and Newer Therapeutic Options.

Curr Pain Headache Rep. 2024-5

[9]
Narrative Review of the Complex Interaction between Pain and Trauma in Children: A Focus on Biological Memory, Preclinical Data, and Epigenetic Processes.

Children (Basel). 2023-7-13

[10]
Global research trends on epigenetics and neuropathic pain: A bibliometric analysis.

Front Mol Neurosci. 2023-4-19

本文引用的文献

[1]
miR-223 Inhibits the Polarization and Recruitment of Macrophages via NLRP3/IL-1 Pathway to Meliorate Neuropathic Pain.

Pain Res Manag. 2021

[2]
Overexpression of miR-378 Alleviates Chronic Sciatic Nerve Injury by Targeting EZH2.

Neurochem Res. 2021-12

[3]
Effect of intrathecal injection of miRNA-138 on neuropathic pain in rats undergoing partial sciatic nerve ligation and its underlying mechanism.

Ann Palliat Med. 2021-6

[4]
Investigation of the role of miR-221 in diabetic peripheral neuropathy and related molecular mechanisms.

Adv Clin Exp Med. 2021-6

[5]
Downregulating lncRNA PVT1 Relieves Astrocyte Overactivation Induced Neuropathic Pain Through Targeting miR-186-5p/CXCL13/CXCR5 Axis.

Neurochem Res. 2021-6

[6]
MiR-122-5p suppresses neuropathic pain development by targeting PDK4.

Neurochem Res. 2021-4

[7]
miR‑142‑3p targets AC9 to regulate sciatic nerve injury‑induced neuropathic pain by regulating the cAMP/AMPK signalling pathway.

Int J Mol Med. 2021-2

[8]
LncRNA NEAT1/miR-128-3p/AQP4 axis regulating spinal cord injury-induced neuropathic pain progression.

J Neuroimmunol. 2021-2-15

[9]
Knockdown of miR-130a-3p alleviates spinal cord injury induced neuropathic pain by activating IGF-1/IGF-1R pathway.

J Neuroimmunol. 2021-2-15

[10]
miR-590-3p Alleviates diabetic peripheral neuropathic pain by targeting RAP1A and suppressing infiltration by the T cells.

Acta Biochim Pol. 2020-12-17

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