• 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

Contribution of neurokinin 1 receptors in the cutaneous orofacial inflammatory pain.

作者信息

Luccarini Philippe, Henry Mélaine, Alvarez Pedro, Gaydier Anne-Marie, Dallel Radhouane

机构信息

INSERM E 0216, Neurobiologie de la Douleur Trigéminale, Faculté de Chirurgie Dentaire, 11 Boulevard Charles de Gaulle, 63000, Clermont-Ferrand, France.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2003 Oct;368(4):320-3. doi: 10.1007/s00210-003-0799-z. Epub 2003 Sep 27.

DOI:10.1007/s00210-003-0799-z
PMID:14517596
Abstract

This study investigated the role of neurokinin 1 receptors (NK1R) in inflammatory cutaneous orofacial pain. The effects of subcutaneous and intracisternal administration of the NK1R antagonist SR140333 on the face rubbing response provoked by injection of 50 micro l of 1.5% formalin into the vibrissa pad were examined. Subcutaneous administration of SR140333 (5, 15, 30 mg/kg) induced a dose-related depressant effect on both the first and second phases of the formalin test. In contrast, intracisternal administration of SR140333 (10, 30, 60, 90 microg) produced a decrease only on the second phase with an apparent ceiling effect at approximately 50%. These data suggest that persistent nociceptive effects associated with orofacial cutaneous inflammation depend at least in part on the activation of NK1R.

摘要

相似文献

1
Contribution of neurokinin 1 receptors in the cutaneous orofacial inflammatory pain.
Naunyn Schmiedebergs Arch Pharmacol. 2003 Oct;368(4):320-3. doi: 10.1007/s00210-003-0799-z. Epub 2003 Sep 27.
2
Intracisternal administration of NR2 antagonists attenuates facial formalin-induced nociceptive behavior in rats.脑池内给予NR2拮抗剂可减轻大鼠面部福尔马林诱导的伤害性反应行为。
J Orofac Pain. 2010 Spring;24(2):203-11.
3
Peripheral administration of NR2 antagonists attenuates orofacial formalin-induced nociceptive behavior in rats.外周给予 NR2 拮抗剂可减轻大鼠福尔马林致口面部疼痛行为。
Prog Neuropsychopharmacol Biol Psychiatry. 2011 Jun 1;35(4):982-6. doi: 10.1016/j.pnpbp.2011.01.018. Epub 2011 Feb 2.
4
Intracisternal NMDA produces analgesia in the orofacial formalin test of freely moving rats.脑池内注射N-甲基-D-天冬氨酸(NMDA)可使自由活动大鼠在口面部福尔马林试验中产生镇痛作用。
Prog Neuropsychopharmacol Biol Psychiatry. 2004 May;28(3):497-503. doi: 10.1016/j.pnpbp.2004.01.001.
5
The non-peptide NK1 receptor antagonist SR140333 produces long-lasting inhibition of neurogenic inflammation, but does not influence acute chemo- or thermonociception in rats.非肽类NK1受体拮抗剂SR140333可对神经源性炎症产生持久抑制作用,但对大鼠的急性化学性或热性疼痛没有影响。
Naunyn Schmiedebergs Arch Pharmacol. 1995 Aug;352(2):201-5. doi: 10.1007/BF00176775.
6
The orofacial formalin test in the mouse: a behavioral model for studying physiology and modulation of trigeminal nociception.小鼠口腔面部福尔马林试验:一种用于研究三叉神经痛觉生理及调节的行为学模型。
J Pain. 2006 Dec;7(12):908-14. doi: 10.1016/j.jpain.2006.04.010.
7
Peripheral substance P and neurokinin-1 receptors have a role in inflammatory and neuropathic orofacial pain models.外周物质 P 和神经激肽-1 受体在炎症性和神经性口腔面部疼痛模型中起作用。
Neuropeptides. 2013 Jun;47(3):199-206. doi: 10.1016/j.npep.2012.10.005. Epub 2012 Nov 22.
8
Intracisternal administration of chemokines facilitated formalin-induced behavioral responses in the orofacial area of freely moving rats.脑池内注射趋化因子可促进自由活动大鼠口腔面部区域对福尔马林诱导的行为反应。
Brain Res Bull. 2005 Jul 15;66(1):50-8. doi: 10.1016/j.brainresbull.2005.03.015.
9
Effects of TNF-alpha injected intracisternally on the nociceptive jaw-opening reflex and orofacial formalin test in freely moving rats.脑池内注射肿瘤坏死因子-α对自由活动大鼠伤害性张口反射和口腔福尔马林试验的影响。
Prog Neuropsychopharmacol Biol Psychiatry. 2003 Jun;27(4):613-8. doi: 10.1016/S0278-5846(03)00049-6.
10
Leukocyte recruitment to peritoneal cavity of rats following formalin injection: role of tachykinin receptors.
J Pharmacol Sci. 2004 Apr;94(4):384-92. doi: 10.1254/jphs.94.384.

引用本文的文献

1
Neuroepithelial control of mucosal inflammation in acute cystitis.神经上皮对急性膀胱炎黏膜炎症的控制。
Sci Rep. 2018 Jul 20;8(1):11015. doi: 10.1038/s41598-018-28634-0.
2
Role of the thalamic submedius nucleus histamine H1 and H 2 and opioid receptors in modulation of formalin-induced orofacial pain in rats.丘脑正中下核组胺H1和H2以及阿片受体在调节大鼠福尔马林诱导的口面部疼痛中的作用。
Naunyn Schmiedebergs Arch Pharmacol. 2015 Oct;388(10):1089-96. doi: 10.1007/s00210-015-1143-0. Epub 2015 Jun 16.
3
Increasing substance P levels in serum and synovial tissues from patients with developmental dysplasia of the hip (DDH).

本文引用的文献

1
Proteinase-activated receptor-2 and hyperalgesia: A novel pain pathway.蛋白酶激活受体-2与痛觉过敏:一条新的疼痛通路。
Nat Med. 2001 Jul;7(7):821-6. doi: 10.1038/89945.
2
Receptor systems mediating c-fos expression within trigeminal nucleus caudalis in animal models of migraine.在偏头痛动物模型中,介导三叉神经尾侧核内c-fos表达的受体系统。
Brain Res Brain Res Rev. 2001 Mar;35(1):20-35. doi: 10.1016/s0165-0173(00)00048-5.
3
Effects of supraspinal administration of PG-SPI and PG-KII, two amphibian tachykinin peptides, on nociception in the rat.
髋关节发育不良(DDH)患者血清和滑膜组织中P物质水平升高。
BMC Musculoskelet Disord. 2014 Mar 19;15:92. doi: 10.1186/1471-2474-15-92.
4
Novel strategies for the treatment of inflammatory hyperalgesia.治疗炎症性痛觉过敏的新策略。
Eur J Clin Pharmacol. 2010 May;66(5):429-44. doi: 10.1007/s00228-010-0784-7. Epub 2010 Feb 13.
两种两栖类速激肽肽PG-SPI和PG-KII脊髓上给药对大鼠痛觉的影响。
Peptides. 2000 Nov;21(11):1611-6. doi: 10.1016/s0196-9781(00)00292-8.
4
Simultaneous activation of N-methyl-D-aspartate and neurokinin-1 receptors modulates c-Fos and Zif/268 expression in the rat trigeminal nucleus caudalis.N-甲基-D-天冬氨酸受体与神经激肽-1受体的同时激活调节大鼠三叉神经尾侧核中c-Fos和Zif/268的表达。
Neuroscience. 2000;98(2):317-23. doi: 10.1016/s0306-4522(00)00122-6.
5
Elevated substance-P-like immunoreactivity levels in spinal dialysates during the formalin test in normal and diabetic rats.正常和糖尿病大鼠在福尔马林试验期间脊髓透析液中P物质样免疫反应性水平升高。
Brain Res. 2000 Feb 21;856(1-2):20-7. doi: 10.1016/s0006-8993(99)02345-8.
6
Tachykinin receptor inhibition and c-Fos expression in the rat brain following formalin-induced pain.福尔马林诱导疼痛后大鼠脑中速激肽受体抑制与c-Fos表达
Neuroscience. 2000;95(3):813-20. doi: 10.1016/s0306-4522(99)00478-9.
7
Distribution of Fos-like immunoreactivity in guinea-pig brain following administration of the neurokinin-1 receptor agonist, [SAR9,MET(O2)11]substance P.给予神经激肽-1受体激动剂[ SAR9,MET(O2)11]P物质后豚鼠脑内Fos样免疫反应性的分布
Neuroscience. 1999;94(2):663-73. doi: 10.1016/s0306-4522(99)00283-3.
8
Evidence for tonic activation of NK-1 receptors during the second phase of the formalin test in the Rat.大鼠福尔马林试验第二阶段中NK-1受体紧张性激活的证据。
J Neurosci. 1999 Aug 1;19(15):6588-98. doi: 10.1523/JNEUROSCI.19-15-06588.1999.
9
Alterations in neurokinin A-, substance P- and calcitonin gene-related peptide immunoreactivities in the caudal trigeminal nucleus of the rat following electrical stimulation of the trigeminal ganglion.三叉神经节电刺激后大鼠尾侧三叉神经核中神经激肽A、P物质和降钙素基因相关肽免疫反应性的变化。
Neurosci Lett. 1999 Feb 19;261(3):179-82. doi: 10.1016/s0304-3940(98)00989-6.
10
Intrathecal substance P-induced thermal hyperalgesia and spinal release of prostaglandin E2 and amino acids.鞘内注射P物质诱导的热痛觉过敏以及脊髓中前列腺素E2和氨基酸的释放。
Neuroscience. 1999 Mar;89(2):525-34. doi: 10.1016/s0306-4522(98)00488-6.