• 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

儿茶酚-O-甲基转移酶(COMT)抑制可降低脊髓伤害性活动。

Catechol-O-methyltransferase (COMT) inhibition reduces spinal nociceptive activity.

机构信息

National Institute of Occupational Health, Oslo, Norway.

出版信息

Neurosci Lett. 2010 Apr 12;473(3):212-5. doi: 10.1016/j.neulet.2010.02.049. Epub 2010 Feb 26.

DOI:10.1016/j.neulet.2010.02.049
PMID:20219633
Abstract

Several variants of the catechol-O-methyltransferase (COMT) gene have recently been linked to pain sensitivity. In the present study, electrophysiological field potential recordings from the dorsal horn in rats were used to examine the spinal effect of reduced COMT activity. The data demonstrated that 30 mg/kg of the COMT inhibitor OR 486 reduced spinal nociceptive responses to painful stimuli (p<or=0.01, OR 486 vs. vehicle) and attenuated the expression of spinal long-term potentiation (LTP), an often studied model for central sensitization (p<or=0.01, HFS vs. HFS+OR 486). Our findings suggest that low COMT activity may have an antinociceptive effect in the spinal cord.

摘要

几种儿茶酚-O-甲基转移酶 (COMT) 基因的变体最近与疼痛敏感性相关联。在本研究中,使用大鼠背角的电生理场电位记录来检查 COMT 活性降低对脊髓的影响。数据表明,30mg/kg 的 COMT 抑制剂 OR 486 降低了对疼痛刺激的脊髓伤害性反应(p<or=0.01,OR 486 与载体相比),并减弱了脊髓长时程增强(LTP)的表达,这是一种常用于研究中枢敏化的模型(p<or=0.01,HFS 与 HFS+OR 486 相比)。我们的研究结果表明,低 COMT 活性可能对脊髓具有镇痛作用。

相似文献

1
Catechol-O-methyltransferase (COMT) inhibition reduces spinal nociceptive activity.儿茶酚-O-甲基转移酶(COMT)抑制可降低脊髓伤害性活动。
Neurosci Lett. 2010 Apr 12;473(3):212-5. doi: 10.1016/j.neulet.2010.02.049. Epub 2010 Feb 26.
2
The direction of synaptic plasticity mediated by C-fibers in spinal dorsal horn is decided by Src-family kinases in microglia: the role of tumor necrosis factor-alpha.小胶质细胞中的 Src 家族激酶决定了脊髓背角中 C 纤维介导的突触可塑性的方向:肿瘤坏死因子-α的作用。
Brain Behav Immun. 2010 Aug;24(6):874-80. doi: 10.1016/j.bbi.2010.01.007. Epub 2010 Jan 29.
3
[Role of phospho-calcium/ calmodulin-dependent protein kinase II in the induction and maintenance of long-term potentiation of C-fiber-evoked field potentials in spinal dorsal horn of the rat].[磷酸钙/钙调蛋白依赖性蛋白激酶II在大鼠脊髓背角C纤维诱发场电位长时程增强的诱导和维持中的作用]
Sheng Li Xue Bao. 2004 Feb 25;56(1):83-8.
4
Protein synthesis inhibition blocks the late-phase LTP of C-fiber evoked field potentials in rat spinal dorsal horn.蛋白质合成抑制可阻断大鼠脊髓背角C纤维诱发场电位的晚期长时程增强。
J Neurophysiol. 2003 May;89(5):2354-9. doi: 10.1152/jn.01027.2002.
5
Increased C-fiber nociceptive input potentiates inhibitory glycinergic transmission in the spinal dorsal horn.C纤维伤害性传入增加增强了脊髓背角的抑制性甘氨酸能传递。
J Pharmacol Exp Ther. 2008 Mar;324(3):1000-10. doi: 10.1124/jpet.107.133470. Epub 2007 Dec 13.
6
Pain behavior and response properties of spinal dorsal horn neurons following experimental diabetic neuropathy in the rat: modulation by nitecapone, a COMT inhibitor with antioxidant properties.大鼠实验性糖尿病神经病变后脊髓背角神经元的疼痛行为和反应特性:具有抗氧化特性的儿茶酚-O-甲基转移酶(COMT)抑制剂硝替卡朋的调节作用
Exp Neurol. 2001 Feb;167(2):425-34. doi: 10.1006/exnr.2000.7574.
7
Non-linear morphine-induced depression of spinal excitation following long-term potentiation of C fibre-evoked spinal field potentials.在C纤维诱发的脊髓场电位长期增强后,吗啡对脊髓兴奋的非线性抑制作用。
Eur J Pain. 2008 Aug;12(6):814-7. doi: 10.1016/j.ejpain.2007.10.016. Epub 2008 Jan 3.
8
Acute nerve injury induces long-term potentiation of C-fiber evoked field potentials in spinal dorsal horn of intact rat.急性神经损伤可诱导完整大鼠脊髓背角中C纤维诱发场电位的长期增强。
Sheng Li Xue Bao. 2004 Oct 25;56(5):591-6.
9
Tumor necrosis factor-alpha induces long-term potentiation of C-fiber evoked field potentials in spinal dorsal horn in rats with nerve injury: the role of NF-kappa B, JNK and p38 MAPK.肿瘤坏死因子-α诱导神经损伤大鼠脊髓背角C纤维诱发场电位的长期增强:核因子-κB、应激活化蛋白激酶和p38丝裂原活化蛋白激酶的作用
Neuropharmacology. 2007 Mar;52(3):708-15. doi: 10.1016/j.neuropharm.2006.09.011. Epub 2006 Nov 2.
10
Local and descending circuits regulate long-term potentiation and zif268 expression in spinal neurons.局部和下行神经回路调节脊髓神经元中的长时程增强和zif268表达。
Eur J Neurosci. 2006 Aug;24(3):761-72. doi: 10.1111/j.1460-9568.2006.04968.x.

引用本文的文献

1
Pain-related single nucleotide polymorphisms: association with lumbar spinal stenosis patient experience and non-surgical treatment outcomes.疼痛相关单核苷酸多态性:与腰椎管狭窄症患者体验及非手术治疗结果的关联
Eur Spine J. 2024 Jun;33(6):2213-2221. doi: 10.1007/s00586-024-08182-0. Epub 2024 Apr 6.
2
Differential Gene Expression in Pain-Related Genes are not Affected by the Presence of Dementia.疼痛相关基因中的差异基因表达不受痴呆症存在的影响。
Pain Manag Nurs. 2024 Apr;25(2):145-151. doi: 10.1016/j.pmn.2023.11.001. Epub 2023 Dec 21.
3
Can Implementation of Genetics and Pharmacogenomics Improve Treatment of Chronic Low Back Pain?
遗传学和药物基因组学的应用能否改善慢性下腰痛的治疗?
Pharmaceutics. 2020 Sep 21;12(9):894. doi: 10.3390/pharmaceutics12090894.
4
Contribution of COMT and BDNF Genotype and Expression to the Risk of Transition From Acute to Chronic Low Back Pain.COMT 和 BDNF 基因型和表达对急性至慢性下腰痛转化风险的贡献。
Clin J Pain. 2020 Jun;36(6):430-439. doi: 10.1097/AJP.0000000000000819.
5
Spinal α -adrenoceptors and neuropathic pain modulation; therapeutic target.脊髓 α-肾上腺素能受体与神经病理性疼痛调制;治疗靶点。
Br J Pharmacol. 2019 Jul;176(14):2366-2381. doi: 10.1111/bph.14580. Epub 2019 Mar 6.
6
Acute Low Back Pain: Differential Somatosensory Function and Gene Expression Compared With Healthy No-Pain Controls.急性下背痛:与健康无痛对照组相比的差异体感功能和基因表达
Clin J Pain. 2016 Nov;32(11):933-939. doi: 10.1097/AJP.0000000000000347.
7
The brain-derived neurotrophic factor (BDNF) val66met polymorphism differentially affects performance on subscales of the Wechsler Memory Scale - Third Edition (WMS-III).脑源性神经营养因子(BDNF)val66met多态性对韦氏记忆量表第三版(WMS-III)各分量表的表现有不同影响。
Front Psychol. 2015 Aug 17;6:1212. doi: 10.3389/fpsyg.2015.01212. eCollection 2015.
8
COMT gene locus: new functional variants.儿茶酚-O-甲基转移酶基因位点:新的功能变异体
Pain. 2015 Oct;156(10):2072-2083. doi: 10.1097/j.pain.0000000000000273.
9
Janus molecule I: dichotomous effects of COMT in neuropathic vs nociceptive pain modalities.Janus 分子 I:COMT 在神经病理性疼痛与伤害性疼痛模式中的双重作用。
CNS Neurol Disord Drug Targets. 2012 May;11(3):222-35. doi: 10.2174/187152712800672490.
10
Plasticity in human motor cortex is in part genetically determined.人类运动皮层的可塑性部分是由基因决定的。
J Physiol. 2011 Jan 15;589(Pt 2):297-306. doi: 10.1113/jphysiol.2010.200600. Epub 2010 Nov 22.