• 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

极低剂量全身性吗啡在持续性疼痛动物模型(弗氏佐剂诱导的关节炎大鼠)中的反常痛觉过敏效应

Paradoxical hyperalgesic effect of exceedingly low doses of systemic morphine in an animal model of persistent pain (Freund's adjuvant-induced arthritic rats).

作者信息

Kayser V, Besson J M, Guilbaud G

出版信息

Brain Res. 1987 Jun 23;414(1):155-7. doi: 10.1016/0006-8993(87)91338-2.

DOI:10.1016/0006-8993(87)91338-2
PMID:3620918
Abstract

The effects of exceedingly low doses of morphine (3-50 micrograms/kg i.v.) were studied upon the vocalization threshold induced by paw pressure in rats with Freund's adjuvant-induced arthritis. The highest dose used (50 micrograms/kg i.v.) clearly induced an analgesic effect. No significant modification of the vocalization threshold was observed with 30 micrograms/kg. By contrast, a significant hyperalgesic effect resulted with doses of 10 down to 3 micrograms/kg. Maximum hyperalgesia was observed with 6 micrograms/kg.

摘要

研究了极低剂量吗啡(静脉注射3 - 50微克/千克)对弗氏佐剂诱导性关节炎大鼠 paw 压力诱导的发声阈值的影响。所使用的最高剂量(静脉注射50微克/千克)明显诱导了镇痛作用。30微克/千克剂量未观察到发声阈值的显著改变。相比之下,10微克/千克至3微克/千克剂量产生了显著的痛觉过敏效应。6微克/千克时观察到最大痛觉过敏。

相似文献

1
Paradoxical hyperalgesic effect of exceedingly low doses of systemic morphine in an animal model of persistent pain (Freund's adjuvant-induced arthritic rats).极低剂量全身性吗啡在持续性疼痛动物模型(弗氏佐剂诱导的关节炎大鼠)中的反常痛觉过敏效应
Brain Res. 1987 Jun 23;414(1):155-7. doi: 10.1016/0006-8993(87)91338-2.
2
The analgesic effects of morphine, but not those of the enkephalinase inhibitor thiorphan, are enhanced in arthritic rats.
Brain Res. 1983 May 9;267(1):131-8. doi: 10.1016/0006-8993(83)91046-6.
3
Cross-tolerance between analgesic low doses of morphine and naloxone in arthritic rats.
Brain Res. 1987 Mar 3;405(1):123-9. doi: 10.1016/0006-8993(87)90996-6.
4
Analgesia produced by low doses of the opiate antagonist naloxone in arthritic rats is reduced in morphine-tolerant animals.
Brain Res. 1986 Apr 16;371(1):37-41. doi: 10.1016/0006-8993(86)90807-3.
5
Increase in the threshold of a nociceptive test induced by naloxone in morphine-tolerant rats.纳洛酮诱导的吗啡耐受大鼠伤害性感受测试阈值升高。
Brain Res. 1985 Oct 7;344(2):360-4. doi: 10.1016/0006-8993(85)90815-7.
6
Behavioural evidence for a peripheral component in the enhanced antinociceptive effect of a low dose of systemic morphine in carrageenin-induced hyperalgesic rats.低剂量全身吗啡对角叉菜胶诱导的痛觉过敏大鼠增强的抗伤害感受作用中周围成分的行为学证据。
Brain Res. 1991 Sep 27;560(1-2):237-44. doi: 10.1016/0006-8993(91)91238-v.
7
Differential effects of specific delta and kappa opioid receptor antagonists on the bidirectional dose-dependent effect of systemic naloxone in arthritic rats, an experimental model of persistent pain.特定δ和κ阿片受体拮抗剂对全身性纳洛酮在关节炎大鼠(一种持续性疼痛的实验模型)中双向剂量依赖性作用的不同影响。
Brain Res. 1993 Oct 1;623(2):201-7. doi: 10.1016/0006-8993(93)91428-u.
8
Further evidence for a bidirectional effect of naloxone on the pain threshold in tolerant and non-tolerant arthritic rats.纳洛酮对耐受和未耐受的关节炎大鼠痛阈双向作用的进一步证据。
Neuropeptides. 1984 Dec;5(1-3):49-52. doi: 10.1016/0143-4179(84)90024-6.
9
Dose-dependent analgesic and hyperalgesic effects of systemic naloxone in arthritic rats.
Brain Res. 1981 Dec 7;226(1-2):344-8. doi: 10.1016/0006-8993(81)91110-0.
10
Differential effects of various doses of morphine and naloxone on two nociceptive test thresholds in arthritic and normal rats.
Pain. 1990 Jun;41(3):353-363. doi: 10.1016/0304-3959(90)90012-3.

引用本文的文献

1
A new acyl derivative of sulfadimethoxine inhibits phagocyte oxidative burst and ameliorates inflammation in a mice model of zymosan-induced generalised inflammation.一种新的磺胺二甲氧嘧啶酰基衍生物可抑制吞噬细胞氧化爆发,并改善酵母聚糖诱导的全身性炎症小鼠模型中的炎症。
Inflammopharmacology. 2023 Dec;31(6):3303-3316. doi: 10.1007/s10787-023-01372-0. Epub 2023 Nov 16.
2
Comparison of Nociceptive Effects of Buprenorphine, Firocoxib, and Meloxicam in a Plantar Incision Model in Sprague-Dawley Rats.布比卡因、非甾体抗炎药(昔布类)和美洛昔康在 Sprague-Dawley 大鼠足底切口模型中对伤害性效应的比较。
J Am Assoc Lab Anim Sci. 2021 Sep 1;60(5):539-548. doi: 10.30802/AALAS-JAALAS-20-000142. Epub 2021 Jul 15.
3
Mu-opioid Receptor (MOR) Biased Agonists Induce Biphasic Dose-dependent Hyperalgesia and Analgesia, and Hyperalgesic Priming in the Rat.
μ 阿片受体(MOR)偏向激动剂诱导大鼠双相剂量依赖性痛觉过敏和镇痛,以及痛觉过敏引发。
Neuroscience. 2018 Dec 1;394:60-71. doi: 10.1016/j.neuroscience.2018.10.015. Epub 2018 Oct 17.
4
Opioid-induced myoclonus and hyperalgesia following a short course of low-dose oral morphine.小剂量口服吗啡短期治疗后出现阿片类药物诱发的肌阵挛和痛觉过敏。
Br J Pain. 2017 Feb;11(1):32-35. doi: 10.1177/2049463716664371. Epub 2016 Aug 22.
5
μ-Opioid receptor 6-transmembrane isoform: A potential therapeutic target for new effective opioids.μ-阿片受体6跨膜异构体:新型有效阿片类药物的潜在治疗靶点。
Prog Neuropsychopharmacol Biol Psychiatry. 2015 Oct 1;62:61-7. doi: 10.1016/j.pnpbp.2014.11.009. Epub 2014 Dec 6.
6
The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain.低剂量纳曲酮(LDN)作为慢性疼痛新型抗炎治疗方法的应用。
Clin Rheumatol. 2014 Apr;33(4):451-9. doi: 10.1007/s10067-014-2517-2. Epub 2014 Feb 15.
7
Dual effect of morphine in long-term social memory in rat.吗啡对大鼠长期社会记忆的双重作用。
Br J Pharmacol. 2013 Apr;168(8):1786-93. doi: 10.1111/bph.12060.
8
A novel alternatively spliced isoform of the mu-opioid receptor: functional antagonism.一种新型的μ阿片受体剪接异构体:功能拮抗。
Mol Pain. 2010 Jun 2;6:33. doi: 10.1186/1744-8069-6-33.
9
Supraspinal Gbetagamma-dependent stimulation of PLCbeta originating from G inhibitory protein-mu opioid receptor-coupling is necessary for morphine induced acute hyperalgesia.源自G抑制蛋白-μ阿片受体偶联的PLCβ的脊髓上Gβγ依赖性刺激对于吗啡诱导的急性痛觉过敏是必需的。
J Neurochem. 2009 Oct;111(1):171-80. doi: 10.1111/j.1471-4159.2009.06308.x. Epub 2009 Jul 27.
10
Low doses of alpha 2-adrenoceptor antagonists augment spinal morphine analgesia and inhibit development of acute and chronic tolerance.低剂量的α2-肾上腺素能受体拮抗剂可增强脊髓吗啡镇痛作用,并抑制急性和慢性耐受性的形成。
Br J Pharmacol. 2008 Dec;155(8):1264-78. doi: 10.1038/bjp.2008.353. Epub 2008 Sep 22.