• 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

一种强效的抗伤害性大麻素,在猴子身上缺乏阿片类替代特性。

A potent antinociceptive cannabinoid which lacks opiate substitution properties in monkeys.

作者信息

Martin B R, Dewey W L, Aceto M D, Adams M D, Earnhardt J T, Carney J M

出版信息

Res Commun Chem Pathol Pharmacol. 1977 Jan;16(1):187-90.

PMID:402685
Abstract

(-)-9-Nor-9beta-hydroxy-hexahydrocannabinol[(-)-9-nor-9beta-OH-HHC] produced hypotension and bradycardia in anesthetized dogs, was a potent antinociceptive agent in the mouse tail-flick and p-phenylquinone abdominal-stretching tests, but did not reverse the effects of morphine withdrawal in dependent monkeys.

摘要

(-)-9-去甲-9β-羟基-六氢大麻酚[(-)-9-去甲-9β-OH-HHC]在麻醉犬中可引起低血压和心动过缓,在小鼠甩尾试验和对苯二酚腹部伸展试验中是一种强效的抗伤害感受剂,但不能逆转依赖猴的吗啡戒断效应。

相似文献

1
A potent antinociceptive cannabinoid which lacks opiate substitution properties in monkeys.一种强效的抗伤害性大麻素,在猴子身上缺乏阿片类替代特性。
Res Commun Chem Pathol Pharmacol. 1977 Jan;16(1):187-90.
2
9-nor-9beta-hydroxyhexahydrocannabinol, a cannabinoid with potent antinociceptive activity: comparisons with morphine.9-去甲-9β-羟基六氢大麻酚,一种具有强效抗伤害感受活性的大麻素:与吗啡的比较。
J Pharmacol Exp Ther. 1977 Feb;200(2):263-70.
3
A comparison of clonidine with morphine for antinociceptive and antiwithdrawal actions.可乐定与吗啡在抗伤害感受和抗戒断作用方面的比较。
J Pharmacol Exp Ther. 1978 Dec;207(3):899-905.
4
Antinociceptive activity of intrathecally administered cannabinoids alone, and in combination with morphine, in mice.鞘内注射大麻素单独及与吗啡联合使用对小鼠的镇痛活性。
J Pharmacol Exp Ther. 1992 Jul;262(1):10-8.
5
Morphine withdrawal modifies antinociceptive effects of acute morphine in rats.吗啡戒断会改变急性吗啡对大鼠的镇痛作用。
Biochem Biophys Res Commun. 2006 Jul 28;346(2):578-82. doi: 10.1016/j.bbrc.2006.05.151. Epub 2006 Jun 5.
6
DREAM ablation selectively alters THC place aversion and analgesia but leaves intact the motivational and analgesic effects of morphine.DREAM消融选择性地改变了四氢大麻酚引起的位置厌恶和镇痛作用,但吗啡的动机和镇痛作用保持不变。
Eur J Neurosci. 2004 Jun;19(11):3033-41. doi: 10.1111/j.0953-816X.2004.03435.x.
7
Modulation of oral morphine antinociceptive tolerance and naloxone-precipitated withdrawal signs by oral Delta 9-tetrahydrocannabinol.口服Δ⁹-四氢大麻酚对口服吗啡镇痛耐受性及纳洛酮诱发戒断症状的调节作用
J Pharmacol Exp Ther. 2003 Jun;305(3):812-7. doi: 10.1124/jpet.102.046870. Epub 2003 Feb 11.
8
Lack of cross-tolerance to the antinociceptive effects of systemic and topical cannabinoids in morphine-tolerant mice.吗啡耐受小鼠对全身和局部大麻素的抗伤害感受作用缺乏交叉耐受性。
Neurosci Lett. 2004 Nov 23;371(2-3):122-7. doi: 10.1016/j.neulet.2004.08.052.
9
Investigation of brain sites mediating cannabinoid-induced antinociception in rats: evidence supporting periaqueductal gray involvement.大鼠中介导大麻素诱导的抗伤害感受的脑区研究:支持导水管周围灰质参与的证据。
J Pharmacol Exp Ther. 1996 Feb;276(2):585-93.
10
Correlation between the in vivo and an in vitro expression of opiate withdrawal precipitated by naloxone: their antagonism by l-(-)-delta9-tetrahydrocannabinol.纳洛酮诱发的体内外阿片戒断反应之间的相关性:L-(-)-δ9-四氢大麻酚对它们的拮抗作用。
J Pharmacol Exp Ther. 1976 Nov;199(2):375-84.

引用本文的文献

1
Toward drugs derived from cannabis.迈向源自大麻的药物。
Naturwissenschaften. 1978 Apr;65(4):174-9. doi: 10.1007/BF00450585.