• 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

Functional blockade of opioid analgesia by orphanin FQ/nociceptin.

作者信息

King M, Chang A, Pasternak G W

机构信息

Cotzias Laboratory of Neuro-Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Biochem Pharmacol. 1998 May 1;55(9):1537-40. doi: 10.1016/s0006-2952(98)00023-9.

DOI:10.1016/s0006-2952(98)00023-9
PMID:10076548
Abstract

Orphanin FQ/nociceptin (OFQ/N) is a recently identified neuropeptide with high affinity for the orphan opioid receptor. OFQ/N blocked morphine analgesia in mice in a dose-dependent manner, as well as the analgesic actions of [D-Pen2, D-Pen5]enkephalin (DPDPE), morphine-6 beta-glucuronide, trans-3,4-dichloro-N-[2-(1-pyrrolindinyl)-cyclohexyl]-benzeneac eta mide, methane sulfonate hydrate (U50,488H) and naloxone benzoylhydrazone. These actions are anti-analgesic, because OFQ/N also blocked clonidine analgesia and OFQ/N was inactive against the inhibition of gastrointestinal transit by morphine. Although OFQ/N was quite potent in these paradigms, two truncated forms, OFQ/N(1-11) and OFQ/N(1-7), were inactive. An antisense oligodeoxynucleotide targeting the first coding exon of KOR-3, the mouse homolog of the orphan opioid receptor, effectively prevented the anti-opioid actions of OFQ/N, confirming the importance of the orphan opioid receptor in this action.

摘要

相似文献

1
Functional blockade of opioid analgesia by orphanin FQ/nociceptin.
Biochem Pharmacol. 1998 May 1;55(9):1537-40. doi: 10.1016/s0006-2952(98)00023-9.
2
Pharmacological characterization of orphanin FQ/nociceptin and its fragments.孤啡肽/痛敏肽及其片段的药理学特性
J Pharmacol Exp Ther. 1997 Aug;282(2):858-65.
3
[Phe1psi(CH2-NH)Gly2]nociceptin-(1-13)-NH2 acts as an agonist of the orphanin FQ/nociceptin receptor in vivo.[苯丙氨酸1ψ(CH2 - NH)甘氨酸2]孤啡肽-(1 - 13)-NH2在体内作为孤啡肽/痛敏肽受体的激动剂。
Eur J Pharmacol. 1998 Sep 11;357(1):R1-3. doi: 10.1016/s0014-2999(98)00567-6.
4
Peripheral orphanin FQ/nociceptin analgesia in the mouse.小鼠外周孤啡肽/痛敏肽镇痛作用
Life Sci. 1999;64(22):2021-8. doi: 10.1016/s0024-3205(99)00149-6.
5
Potentiation of opioid analgesia in dopamine2 receptor knock-out mice: evidence for a tonically active anti-opioid system.多巴胺2受体基因敲除小鼠中阿片类镇痛作用的增强:存在持续激活的抗阿片系统的证据。
J Neurosci. 2001 Oct 1;21(19):7788-92. doi: 10.1523/JNEUROSCI.21-19-07788.2001.
6
Functional antagonism of mu-, delta- and kappa-opioid antinociception by orphanin FQ.孤啡肽对μ、δ和κ阿片类镇痛作用的功能性拮抗
Neurosci Lett. 1996 Aug 23;214(2-3):131-4. doi: 10.1016/0304-3940(96)12917-7.
7
Roles of mu, delta and kappa opioid receptors in spinal and supraspinal mediation of gastrointestinal transit effects and hot-plate analgesia in the mouse.μ、δ和κ阿片受体在小鼠胃肠道转运效应和热板镇痛的脊髓及脊髓上介导中的作用。
J Pharmacol Exp Ther. 1984 Aug;230(2):341-8.
8
[Antagonistic effect of orphanin FQ on morphine analgesia in rat brain].[孤啡肽对大鼠脑内吗啡镇痛的拮抗作用]
Sheng Li Xue Bao. 1997 Jun;49(3):333-8.
9
Orphanin FQ/nociceptin analgesia in the rat.孤啡肽/痛敏肽在大鼠中的镇痛作用。
Brain Res. 1998 May 11;792(2):327-30. doi: 10.1016/s0006-8993(97)01490-x.
10
Spinal analgesic activity of orphanin FQ/nociceptin and its fragments.孤啡肽/痛敏肽及其片段的脊髓镇痛活性。
Neurosci Lett. 1997 Feb 21;223(2):113-6. doi: 10.1016/s0304-3940(97)13414-0.

引用本文的文献

1
Therapeutic potentials of NOP and MOP receptor coactivation for the treatment of pain and opioid abuse.NOP 和 MOP 受体共激活在治疗疼痛和阿片类药物滥用方面的治疗潜力。
J Neurosci Res. 2022 Jan;100(1):191-202. doi: 10.1002/jnr.24624. Epub 2020 Apr 7.
2
The Cholinergic System as a Treatment Target for Opioid Use Disorder.胆碱能系统作为阿片类药物使用障碍的治疗靶点。
CNS Drugs. 2018 Nov;32(11):981-996. doi: 10.1007/s40263-018-0572-y.
3
Bifunctional peptide-based opioid agonist/nociceptin antagonist ligand for dual treatment of nociceptive and neuropathic pain.
用于双重治疗伤害性疼痛和神经性疼痛的基于双功能肽的阿片样物质激动剂/孤啡肽拮抗剂配体。
Pain. 2017 Mar;158(3):505-515. doi: 10.1097/j.pain.0000000000000790.
4
Mediation of buprenorphine analgesia by a combination of traditional and truncated mu opioid receptor splice variants.传统型和截短型μ阿片受体剪接变体联合介导丁丙诺啡镇痛作用。
Synapse. 2016 Oct;70(10):395-407. doi: 10.1002/syn.21914. Epub 2016 Jul 12.
5
Central N/OFQ-NOP Receptor System in Pain Modulation.疼痛调节中的中枢N/OFQ-NOP受体系统。
Adv Pharmacol. 2016;75:217-43. doi: 10.1016/bs.apha.2015.10.001. Epub 2015 Dec 17.
6
Revolution in GPCR signalling: opioid receptor heteromers as novel therapeutic targets: IUPHAR review 10.G蛋白偶联受体信号传导的革命:阿片受体异聚体作为新型治疗靶点:IUPHAR综述10
Br J Pharmacol. 2014 Sep;171(18):4155-76. doi: 10.1111/bph.12798.
7
Functional plasticity of the N/OFQ-NOP receptor system determines analgesic properties of NOP receptor agonists.N/OFQ-NOP受体系统的功能可塑性决定了NOP受体激动剂的镇痛特性。
Br J Pharmacol. 2014 Aug;171(16):3777-800. doi: 10.1111/bph.12744.
8
Disease-specific heteromerization of G-protein-coupled receptors that target drugs of abuse.针对滥用药物的 G 蛋白偶联受体的疾病特异性异源二聚化。
Prog Mol Biol Transl Sci. 2013;117:207-65. doi: 10.1016/B978-0-12-386931-9.00009-X.
9
Nociceptin/orphanin FQ blocks the antinociception induced by mu, kappa and delta opioid agonists on the cold water tail-flick test.痛敏肽/孤啡肽在冷水甩尾试验中可阻断μ、κ和δ阿片类激动剂诱导的抗伤害感受作用。
Eur J Pharmacol. 2007 Feb 14;557(1):32-6. doi: 10.1016/j.ejphar.2006.11.001. Epub 2006 Nov 10.
10
Effect of novel nociceptin/orphanin FQ-NOP receptor ligands on ethanol drinking in alcohol-preferring msP rats.新型孤啡肽/孤啡肽FQ - NOP受体配体对偏爱酒精的msP大鼠乙醇饮用的影响。
Peptides. 2006 Dec;27(12):3299-306. doi: 10.1016/j.peptides.2006.09.007.