• 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

A preliminary investigation of the mechanisms underlying cannabinoid tolerance in the mouse vas deferens.

作者信息

Pertwee R G, Griffin G

机构信息

Department of Biomedical Sciences, Marischal College, University of Aberdeen, Scotland, UK.

出版信息

Eur J Pharmacol. 1995 Jan 5;272(1):67-72. doi: 10.1016/0014-2999(94)00617-g.

DOI:10.1016/0014-2999(94)00617-g
PMID:7713151
Abstract

Vasa deferentia taken from mice treated with delta 9-tetrahydrocannabinol (20 mg/kg i.p., once daily for 2 days) showed tolerance to the inhibitory effect of the cannabinoid, R-(+)-arachidonyl-1'-hydroxy-2'-propylamide, on electrically evoked twitches. This treatment did not induce tolerance to the inhibitory effects on the twitch response of morphine or clonidine or of selective mu-, delta- or kappa-opioid receptor agonists. Nor did it affect the contractile potencies of noradrenaline or beta,gamma-methylene-L-ATP. We suggest that cannabinoid tolerance in the vas deferens is attributable neither to downregulation of opioid receptors or alpha 2-adrenoceptors nor to an increased sensitivity of this tissue to its main contractile transmitters noradrenaline and ATP. A concentration of delta 9-tetrahydrocannabinol that inhibits electrically evoked twitches of the vas deferens (100 nM) did not alter the ability of noradrenaline or beta,gamma-methylene-L-ATP to induce contractions suggesting that delta 9-tetrahydrocannabinol inhibits the twitch response by acting prejunctionally.

摘要

相似文献

1
A preliminary investigation of the mechanisms underlying cannabinoid tolerance in the mouse vas deferens.
Eur J Pharmacol. 1995 Jan 5;272(1):67-72. doi: 10.1016/0014-2999(94)00617-g.
2
Evidence that the plant cannabinoid Delta9-tetrahydrocannabivarin is a cannabinoid CB1 and CB2 receptor antagonist.有证据表明植物大麻素Δ9-四氢大麻酚是一种大麻素CB1和CB2受体拮抗剂。
Br J Pharmacol. 2005 Dec;146(7):917-26. doi: 10.1038/sj.bjp.0706414.
3
Effect of opioid receptor subtype-selective agonists on purinergic and adrenergic components of neurogenic contractions of mouse vas deferens.阿片受体亚型选择性激动剂对小鼠输精管神经源性收缩中嘌呤能和肾上腺素能成分的影响。
Br J Pharmacol. 1993 Feb;108(2):443-7. doi: 10.1111/j.1476-5381.1993.tb12823.x.
4
Effects of chronic drug treatment on the sensitivity of mouse vas deferens to drugs.慢性药物治疗对小鼠输精管药物敏感性的影响。
Eur J Pharmacol. 1985 Dec 3;118(3):253-61. doi: 10.1016/0014-2999(85)90136-0.
5
Effects of two endogenous fatty acid ethanolamides on mouse vasa deferentia.两种内源性脂肪酸乙醇酰胺对小鼠输精管的作用。
Eur J Pharmacol. 1994 Jul 1;259(2):115-20. doi: 10.1016/0014-2999(94)90499-5.
6
Postjunctional inhibition of contractor responses in the mouse vas deferens by rat and human calcitonin gene-related peptides (CGRP).大鼠和人降钙素基因相关肽(CGRP)对小鼠输精管收缩反应的接头后抑制作用
Br J Pharmacol. 1986 May;88(1):173-80. doi: 10.1111/j.1476-5381.1986.tb09484.x.
7
The psychoactive plant cannabinoid, Delta9-tetrahydrocannabinol, is antagonized by Delta8- and Delta9-tetrahydrocannabivarin in mice in vivo.精神活性植物大麻素Δ9-四氢大麻酚在小鼠体内受到Δ8-和Δ9-四氢大麻二酚的拮抗作用。
Br J Pharmacol. 2007 Mar;150(5):586-94. doi: 10.1038/sj.bjp.0707124. Epub 2007 Jan 22.
8
Two phases of contractile response in rat isolated vas deferens and their regulation by adenosine and alpha-receptors.大鼠离体输精管收缩反应的两个阶段及其受腺苷和α受体的调节
Eur J Pharmacol. 1989 Aug 29;167(3):323-31. doi: 10.1016/0014-2999(89)90441-x.
9
[Cys(O2NH2)2]enkephalin analogues and dalargin: selectivity for delta-opioid receptors.[半胱氨酸(O2NH2)2]脑啡肽类似物与达乐精:对δ阿片受体的选择性
Eur J Pharmacol. 1996 May 23;304(1-3):99-108. doi: 10.1016/0014-2999(96)00083-0.
10
Pharmacological characterisation of cannabinoid CB(1) receptors in the rat and mouse.大鼠和小鼠中大麻素CB(1)受体的药理学特性
Eur J Pharmacol. 2000 Mar 10;391(1-2):151-61. doi: 10.1016/s0014-2999(00)00062-5.

引用本文的文献

1
O-1057, a potent water-soluble cannabinoid receptor agonist with antinociceptive properties.O-1057,一种具有抗伤害感受特性的强效水溶性大麻素受体激动剂。
Br J Pharmacol. 2000 Apr;129(8):1577-84. doi: 10.1038/sj.bjp.0703245.
2
An investigation into the structural determinants of cannabinoid receptor ligand efficacy.大麻素受体配体效能的结构决定因素研究。
Br J Pharmacol. 1999 Apr;126(7):1575-84. doi: 10.1038/sj.bjp.0702469.
3
Evidence for the presence of cannabinoid CB1 receptors in mouse urinary bladder.小鼠膀胱中存在大麻素CB1受体的证据。
Br J Pharmacol. 1996 Aug;118(8):2053-8. doi: 10.1111/j.1476-5381.1996.tb15643.x.