• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基因和表观遗传过程作为潜在的疼痛靶点。

Genes and epigenetic processes as prospective pain targets.

作者信息

Crow Megan, Denk Franziska, McMahon Stephen B

机构信息

Wolfson Centre for Age-Related Diseases, King's College London, London SE1 1UL, UK.

出版信息

Genome Med. 2013 Feb 15;5(2):12. doi: 10.1186/gm416. eCollection 2013.

DOI:10.1186/gm416
PMID:23409739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3706821/
Abstract

Chronic pain affects approximately one in five adults, resulting in a greatly reduced quality of life and a higher risk of developing co-morbidities such as depression. Available treatments often provide inadequate pain relief, but it is hoped that through deeper understanding of the molecular mechanisms underlying chronic pain states we can discover new and improved therapies. Although genetic research has flourished over the past decade and has identified many key genes in pain processing, the budding field of epigenetics promises to provide new insights and a more dynamic view of pain regulation. This review gives an overview of basic mechanisms and current therapies to treat pain, and discusses the clinical and preclinical evidence for the contribution of genetic and epigenetic factors, with a focus on how this knowledge can affect drug development.

摘要

慢性疼痛影响着约五分之一的成年人,导致生活质量大幅下降,并增加了患抑郁症等共病的风险。现有的治疗方法往往无法充分缓解疼痛,但人们希望通过更深入地了解慢性疼痛状态背后的分子机制,能够发现新的、更有效的治疗方法。尽管基因研究在过去十年中蓬勃发展,已经确定了许多疼痛处理中的关键基因,但新兴的表观遗传学领域有望提供新的见解和更动态的疼痛调节观点。本文综述了疼痛治疗的基本机制和当前疗法,并讨论了基因和表观遗传因素作用的临床和临床前证据,重点关注这些知识如何影响药物开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/d5b322e46664/gm416-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/2fc7dbbce640/gm416-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/c184dd669592/gm416-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/d5b322e46664/gm416-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/2fc7dbbce640/gm416-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/c184dd669592/gm416-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3b/3706821/d5b322e46664/gm416-3.jpg

相似文献

1
Genes and epigenetic processes as prospective pain targets.基因和表观遗传过程作为潜在的疼痛靶点。
Genome Med. 2013 Feb 15;5(2):12. doi: 10.1186/gm416. eCollection 2013.
2
Epigenetics: a promising paradigm for better understanding and managing pain.表观遗传学:更好地理解和管理疼痛的有希望的范例。
J Pain. 2013 Jun;14(6):549-57. doi: 10.1016/j.jpain.2013.01.772. Epub 2013 Apr 19.
3
Epigenetics and the transition from acute to chronic pain.表观遗传学与急性痛向慢性痛的转变。
Pain Med. 2012 Nov;13(11):1474-90. doi: 10.1111/j.1526-4637.2012.01488.x. Epub 2012 Sep 14.
4
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
5
[Epigenetics' implication in autism spectrum disorders: A review].[表观遗传学在自闭症谱系障碍中的影响:综述]
Encephale. 2017 Aug;43(4):374-381. doi: 10.1016/j.encep.2016.07.007. Epub 2016 Sep 28.
6
7
Antiepileptic drugs for chronic non-cancer pain in children and adolescents.用于儿童和青少年慢性非癌性疼痛的抗癫痫药物。
Cochrane Database Syst Rev. 2017 Aug 5;8(8):CD012536. doi: 10.1002/14651858.CD012536.pub2.
8
Targeting epigenetic mechanisms for pain relief.针对表观遗传机制缓解疼痛。
Curr Opin Pharmacol. 2012 Feb;12(1):35-41. doi: 10.1016/j.coph.2011.10.012. Epub 2011 Nov 3.
9
Neuroimaging of pain: advances and future prospects.疼痛的神经影像学:进展与未来展望。
J Pain. 2008 Jul;9(7):567-79. doi: 10.1016/j.jpain.2008.02.008. Epub 2008 May 2.
10
Recent developments in epigenetics of acute and chronic kidney diseases.急性和慢性肾脏疾病表观遗传学的最新进展。
Kidney Int. 2015 Aug;88(2):250-61. doi: 10.1038/ki.2015.148. Epub 2015 May 20.

引用本文的文献

1
Exploring the epigenetic modifications of the RONS-TRPA1-CGRP axis in migraine pathophysiology.探索偏头痛病理生理学中活性氧-瞬时受体电位锚蛋白1-降钙素基因相关肽轴的表观遗传修饰。
J Headache Pain. 2025 Sep 1;26(1):191. doi: 10.1186/s10194-025-02114-z.
2
A novel SIRT1 activator attenuates neuropathic pain by inhibiting spinal neuronal activation via the SIRT1-mGluR1/5 pathway.一种新型SIRT1激活剂通过SIRT1-mGluR1/5途径抑制脊髓神经元激活来减轻神经性疼痛。
Cell Biol Toxicol. 2025 Jan 8;41(1):24. doi: 10.1007/s10565-024-09970-6.
3
Intraoperative nitrous oxide inhalation to prevent chronic postsurgical pain in video-assisted thoracoscopic surgery: a prospective observational cohort study.

本文引用的文献

1
Genes contributing to pain sensitivity in the normal population: an exome sequencing study.正常人群疼痛敏感性相关基因:外显子组测序研究。
PLoS Genet. 2012;8(12):e1003095. doi: 10.1371/journal.pgen.1003095. Epub 2012 Dec 20.
2
p300 exerts an epigenetic role in chronic neuropathic pain through its acetyltransferase activity in rats following chronic constriction injury (CCI).p300 通过其在慢性缩窄性损伤(CCI)后大鼠中的乙酰转移酶活性发挥在慢性神经性疼痛中的表观遗传作用。
Mol Pain. 2012 Nov 23;8:84. doi: 10.1186/1744-8069-8-84.
3
Importance of epigenetic mechanisms in visceral pain induced by chronic water avoidance stress.
术中吸入一氧化二氮预防电视辅助胸腔镜手术慢性术后疼痛:一项前瞻性观察队列研究。
J Thorac Dis. 2024 Aug 31;16(8):5110-5121. doi: 10.21037/jtd-24-556. Epub 2024 Aug 21.
4
Deciphering nociplastic pain: clinical features, risk factors and potential mechanisms.解析神经病理性疼痛:临床特征、危险因素和潜在机制。
Nat Rev Neurol. 2024 Jun;20(6):347-363. doi: 10.1038/s41582-024-00966-8. Epub 2024 May 16.
5
The Role of the Brain-Derived Neurotrophic Factor in Chronic Pain: Links to Central Sensitization and Neuroinflammation.脑源性神经营养因子在慢性疼痛中的作用:与中枢敏化和神经炎症的关联。
Biomolecules. 2024 Jan 5;14(1):71. doi: 10.3390/biom14010071.
6
Narrative Review of the Complex Interaction between Pain and Trauma in Children: A Focus on Biological Memory, Preclinical Data, and Epigenetic Processes.儿童疼痛与创伤之间复杂相互作用的叙述性综述:聚焦生物记忆、临床前数据和表观遗传过程
Children (Basel). 2023 Jul 13;10(7):1217. doi: 10.3390/children10071217.
7
Epigenetic Connections of the TRPA1 Ion Channel in Pain Transmission and Neurogenic Inflammation - a Therapeutic Perspective in Migraine?TRPA1 离子通道在疼痛传递和神经源性炎症中的表观遗传学关联——偏头痛的治疗新视角?
Mol Neurobiol. 2023 Oct;60(10):5578-5591. doi: 10.1007/s12035-023-03428-2. Epub 2023 Jun 16.
8
Intraganglionic reactive oxygen species mediate inflammatory pain and hyperalgesia through TRPA1 in the rat.神经节内活性氧通过大鼠的TRPA1介导炎性疼痛和痛觉过敏。
Front Pain Res (Lausanne). 2023 May 30;4:1204057. doi: 10.3389/fpain.2023.1204057. eCollection 2023.
9
REAC Antalgic Neuro Modulation in Chronic Post Herpetic Neuralgia.慢性带状疱疹后神经痛中的REAC止痛神经调制
J Pers Med. 2023 Apr 11;13(4):653. doi: 10.3390/jpm13040653.
10
The upregulation of NLRP3 inflammasome in dorsal root ganglion by ten-eleven translocation methylcytosine dioxygenase 2 (TET2) contributed to diabetic neuropathic pain in mice.TET2 通过上调背根神经节中 NLRP3 炎性小体导致小鼠糖尿病神经病理性疼痛。
J Neuroinflammation. 2022 Dec 16;19(1):302. doi: 10.1186/s12974-022-02669-7.
慢性回避水应激引起内脏痛的表观遗传机制的重要性。
Psychoneuroendocrinology. 2013 Jun;38(6):898-906. doi: 10.1016/j.psyneuen.2012.09.016. Epub 2012 Oct 22.
4
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.与北欧人腰椎间盘退变相关的新型遗传变异:4600 例受试者的荟萃分析。
Ann Rheum Dis. 2013 Jul;72(7):1141-8. doi: 10.1136/annrheumdis-2012-201551. Epub 2012 Sep 19.
5
An essential role for histone deacetylase 4 in synaptic plasticity and memory formation.组蛋白去乙酰化酶 4 在突触可塑性和记忆形成中的重要作用。
J Neurosci. 2012 Aug 8;32(32):10879-86. doi: 10.1523/JNEUROSCI.2089-12.2012.
6
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people.在 14002 个人中对 202 个药物靶标基因进行测序,发现了大量罕见的功能变异。
Science. 2012 Jul 6;337(6090):100-4. doi: 10.1126/science.1217876. Epub 2012 May 17.
7
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.人类外显子组深度测序中罕见编码变异的进化和功能影响。
Science. 2012 Jul 6;337(6090):64-9. doi: 10.1126/science.1219240. Epub 2012 May 17.
8
Pain genetics: past, present and future.疼痛遗传学:过去、现在和未来。
Trends Genet. 2012 Jun;28(6):258-66. doi: 10.1016/j.tig.2012.02.004. Epub 2012 Mar 28.
9
The expression of spinal methyl-CpG-binding protein 2, DNA methyltransferases and histone deacetylases is modulated in persistent pain states.脊髓甲基化CpG 结合蛋白 2、DNA 甲基转移酶和组蛋白去乙酰化酶的表达在持续性疼痛状态中受到调节。
Mol Pain. 2012 Feb 27;8:14. doi: 10.1186/1744-8069-8-14.
10
Imaging the neural correlates of neuropathic pain and pleasurable relief associated with inherited erythromelalgia in a single subject with quantitative arterial spin labelling.应用定量动脉自旋标记技术对单例遗传性红细胞增多性肢痛症患者的神经痛和快感缓解的神经相关变化进行成像。
Pain. 2012 May;153(5):1122-1127. doi: 10.1016/j.pain.2011.12.012. Epub 2012 Feb 24.