• 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

脊髓注射腺嘌呤对大鼠炎症模型中背角神经元反应的影响。

Effects of spinally administered adenine on dorsal horn neuronal responses in a rat model of inflammation.

作者信息

Matthews Elizabeth A, Dickenson Anthony H

机构信息

Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.

出版信息

Neurosci Lett. 2004 Feb 19;356(3):211-4. doi: 10.1016/j.neulet.2003.11.057.

DOI:10.1016/j.neulet.2003.11.057
PMID:15036632
Abstract

A novel G-protein-coupled receptor with adenine identified as the endogenous ligand has recently been described. In vivo electrophysiological techniques in the rat were used to record the response of dorsal horn neurones in response to transcutaneous electrical stimulation to the hindpaw receptive field. Spinal adenine (1-1000 microg) exerted facilitatory effects on the electrically-evoked neuronal responses, in a mildly dose-related manner. After establishment of carrageenan-induced inflammation to the hindpaw this excitatory effect of adenine was still apparent, yet reduced. C-fibre-evoked responses and other nociceptive related measures were most susceptible to the effects of adenine, whereas non-nociceptive Abeta-fibre evoked activity remained unaffected. Thus, activation of the adenine receptor site, via spinally applied adenine, suggests a pronociceptive role in nociceptive sensory transmission.

摘要

最近描述了一种新型的G蛋白偶联受体,已确定腺嘌呤为其内源性配体。在大鼠中采用体内电生理技术记录背角神经元对后爪感受野经皮电刺激的反应。脊髓内注射腺嘌呤(1 - 1000微克)以轻度剂量相关的方式对电诱发的神经元反应产生促进作用。在角叉菜胶诱导后爪炎症形成后,腺嘌呤的这种兴奋作用仍然明显,但有所减弱。C纤维诱发反应和其他伤害性相关指标对腺嘌呤的作用最为敏感,而非伤害性Aβ纤维诱发的活动则不受影响。因此,通过脊髓内应用腺嘌呤激活腺嘌呤受体位点表明其在伤害性感觉传递中具有促伤害性作用。

相似文献

1
Effects of spinally administered adenine on dorsal horn neuronal responses in a rat model of inflammation.脊髓注射腺嘌呤对大鼠炎症模型中背角神经元反应的影响。
Neurosci Lett. 2004 Feb 19;356(3):211-4. doi: 10.1016/j.neulet.2003.11.057.
2
The Cav2.3 calcium channel antagonist SNX-482 reduces dorsal horn neuronal responses in a rat model of chronic neuropathic pain.Cav2.3钙通道拮抗剂SNX-482可降低慢性神经性疼痛大鼠模型中背角神经元的反应。
Eur J Neurosci. 2007 Jun;25(12):3561-9. doi: 10.1111/j.1460-9568.2007.05605.x.
3
Descending serotonergic facilitation mediated through rat spinal 5HT3 receptors is unaltered following carrageenan inflammation.通过大鼠脊髓5HT3受体介导的下行5-羟色胺能易化在角叉菜胶炎症后未发生改变。
Neurosci Lett. 2004 May 6;361(1-3):229-31. doi: 10.1016/j.neulet.2003.12.069.
4
Inhibition of peripheral vanilloid TRPV1 receptors reduces noxious heat-evoked responses of dorsal horn neurons in naïve, carrageenan-inflamed and neuropathic rats.抑制外周香草酸瞬时受体电位阳离子通道亚家族V成员1(TRPV1)受体可降低正常、角叉菜胶致炎和神经性大鼠背角神经元的伤害性热诱发反应。
Eur J Neurosci. 2005 Jul;22(2):361-70. doi: 10.1111/j.1460-9568.2005.04227.x.
5
Evidence of a role for descending serotonergic facilitation in a rat model of cancer-induced bone pain.下行5-羟色胺能易化在癌症诱导的骨痛大鼠模型中的作用证据。
Neurosci Lett. 2006 Jan 30;393(2-3):237-42. doi: 10.1016/j.neulet.2005.09.073. Epub 2005 Oct 25.
6
Gabapentin depresses C-fiber-evoked field potentials in rat spinal dorsal horn only after induction of long-term potentiation.加巴喷丁仅在诱导长期增强后才会抑制大鼠脊髓背角中C纤维诱发的场电位。
Exp Neurol. 2006 Dec;202(2):280-6. doi: 10.1016/j.expneurol.2006.06.002. Epub 2006 Jul 20.
7
Anti-hyperalgesic effects of intrathecally administered neuropeptide W-23, and neuropeptide B, in tests of inflammatory pain in rats.鞘内注射神经肽W-23和神经肽B在大鼠炎性疼痛测试中的抗痛觉过敏作用
Brain Res. 2005 May 31;1045(1-2):97-106. doi: 10.1016/j.brainres.2005.03.027. Epub 2005 Apr 21.
8
Selective ablation of dorsal horn NK1 expressing cells reveals a modulation of spinal alpha2-adrenergic inhibition of dorsal horn neurones.对表达NK1的背角细胞进行选择性消融,揭示了脊髓α2-肾上腺素能对背角神经元抑制作用的一种调节。
Neuropharmacology. 2008 Jun;54(8):1208-14. doi: 10.1016/j.neuropharm.2008.03.014. Epub 2008 Apr 8.
9
ReN-1869 [(R)-1-(3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-propyl)-3-piperidine carboxylic acid], a novel histamine H1 receptor antagonist, produces potent and selective antinociceptive effects on dorsal horn neurons after inflammation and neuropathy.ReN-1869 [(R)-1-(3-(10,11-二氢-5H-二苯并[a,d]环庚烯-5-亚基)-1-丙基)-3-哌啶甲酸],一种新型组胺H1受体拮抗剂,对炎症和神经病变后的背角神经元产生强效且选择性的抗伤害感受作用。
J Pharmacol Exp Ther. 2004 Jun;309(3):1230-8. doi: 10.1124/jpet.103.063511. Epub 2004 Feb 26.
10
Effects of spinally administered P2X receptor agonists and antagonists on the responses of dorsal horn neurones recorded in normal, carrageenan-inflamed and neuropathic rats.脊髓注射P2X受体激动剂和拮抗剂对正常、角叉菜胶致炎和神经性大鼠背角神经元反应的影响。
Br J Pharmacol. 2000 Jan;129(2):351-9. doi: 10.1038/sj.bjp.0703047.

引用本文的文献

1
Adenine attenuates the Ca(2+) contraction-signaling pathway via adenine receptor-mediated signaling in rat vascular smooth muscle cells.腺嘌呤通过大鼠血管平滑肌细胞中腺嘌呤受体介导的信号传导减弱Ca(2+)收缩信号通路。
Naunyn Schmiedebergs Arch Pharmacol. 2016 Sep;389(9):999-1007. doi: 10.1007/s00210-016-1264-0. Epub 2016 Jun 18.
2
Characterization of new G protein-coupled adenine receptors in mouse and hamster.鉴定新型 G 蛋白偶联腺嘌呤受体在小鼠和仓鼠中的特性。
Purinergic Signal. 2013 Sep;9(3):415-26. doi: 10.1007/s11302-013-9360-9. Epub 2013 Apr 23.
3
The rat adenine receptor: pharmacological characterization and mutagenesis studies to investigate its putative ligand binding site.
大鼠腺嘌呤受体:药理学特性及突变研究以探讨其假定的配体结合位点。
Purinergic Signal. 2013 Sep;9(3):367-81. doi: 10.1007/s11302-013-9355-6. Epub 2013 Feb 15.