• 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

布瑞马佐辛诱导大鼠向后行走行为是通过阿片κ受体介导的。

Bremazocine-induced backwards walking behavior in rats is mediated via opioid kappa receptors.

作者信息

Shearman G T, Stenfors C

出版信息

Pharmacol Biochem Behav. 1986 Apr;24(4):861-3. doi: 10.1016/0091-3057(86)90426-0.

DOI:10.1016/0091-3057(86)90426-0
PMID:3012599
Abstract

Bremazocine dose-dependently induced backwards walking behavior in rats after its SC injection. Only the (-) but not the (+) enantiomer induced backwards walking. Pretreatment with either naloxone or MR 2266 reduced the bremazocine-induced backwards walking. MR 2266 was at least ten times more potent than naloxone. These findings suggest that bremazocine-induced backwards walking is mediated via an agonistic action of the drug with opioid kappa receptors. The data may contribute to the discussion concerning opioid kappa receptors and the psychotomimetic effects of some opioid analgesic drugs.

摘要

布雷马佐辛皮下注射后能剂量依赖性地诱导大鼠出现向后行走行为。只有(-)对映体而非(+)对映体能诱导向后行走。用纳洛酮或MR 2266预处理可减少布雷马佐辛诱导的向后行走。MR 2266的效力至少比纳洛酮强十倍。这些发现表明,布雷马佐辛诱导的向后行走是通过该药物与阿片κ受体的激动作用介导的。这些数据可能有助于有关阿片κ受体和某些阿片类镇痛药拟精神病作用的讨论。

相似文献

1
Bremazocine-induced backwards walking behavior in rats is mediated via opioid kappa receptors.布瑞马佐辛诱导大鼠向后行走行为是通过阿片κ受体介导的。
Pharmacol Biochem Behav. 1986 Apr;24(4):861-3. doi: 10.1016/0091-3057(86)90426-0.
2
Elevation of serum corticosterone in rats by bremazocine, a kappa-opioid agonist.κ-阿片受体激动剂布瑞马唑辛使大鼠血清皮质酮水平升高。
J Pharm Pharmacol. 1984 May;36(5):345-6. doi: 10.1111/j.2042-7158.1984.tb04392.x.
3
Diuretic effect of bremazocine, a kappa-opioid with central and peripheral sites of action.布瑞马佐辛的利尿作用,一种具有中枢和外周作用位点的κ阿片类药物。
J Pharmacol Exp Ther. 1989 Sep;250(3):992-9.
4
Opioid kappa receptors and the secretion of prolactin (PRL) and growth hormone (GH) in the rat. II. GH and PRL release-inhibiting effects of the opioid kappa receptor agonists bremazocine and U-50,488.阿片κ受体与大鼠催乳素(PRL)和生长激素(GH)的分泌。II. 阿片κ受体激动剂布马佐辛和U-50,488对GH和PRL释放的抑制作用
Neuroendocrinology. 1986;42(1):82-7. doi: 10.1159/000124253.
5
Opioid kappa receptors and the secretion of prolactin (PRL) and growth hormone (GH) in the rat. I. Effects of opioid kappa receptor agonists bremazocine and U-50,488 on secretion of PRL and GH: comparison with morphine.
Neuroendocrinology. 1986;42(1):75-81. doi: 10.1159/000124252.
6
Opiate control of spontaneous locomotor activity in a urodele amphibian.阿片类物质对一种有尾两栖动物自发运动活动的控制
Pharmacol Biochem Behav. 1989 Dec;34(4):753-7. doi: 10.1016/0091-3057(89)90270-0.
7
A comparative study of the respiratory depressant and analgesic effects of bremazocine, a kappa-agonist.κ-激动剂布马佐辛的呼吸抑制和镇痛作用的比较研究
Life Sci. 1983;33 Suppl 1:579-81. doi: 10.1016/0024-3205(83)90569-6.
8
Kappa-opiates and urination: pharmacological evidence for an endogenous role of the kappa-opiate receptor in fluid and electrolyte balance.κ-阿片类药物与排尿:κ-阿片受体在体液和电解质平衡中内源性作用的药理学证据。
Eur J Pharmacol. 1984 Dec 15;107(1):1-10. doi: 10.1016/0014-2999(84)90084-0.
9
The influence of the kappa-agonist bremazocine on ingestive behaviour in mice and rats.κ-激动剂布马佐辛对小鼠和大鼠摄食行为的影响。
Arch Int Pharmacodyn Ther. 1983 Mar;262(1):4-12.
10
Bremazocine causes sympatho-inhibition and hypotension in rabbits by activating peripheral kappa-receptors.
J Cardiovasc Pharmacol. 1986 May-Jun;8(3):470-5. doi: 10.1097/00005344-198605000-00005.

引用本文的文献

1
Observational analysis of the effects of kappa opioid agonists an open field behaviour in the rat.κ阿片受体激动剂对大鼠旷场行为影响的观察性分析
Psychopharmacology (Berl). 1988;94(2):248-53. doi: 10.1007/BF00176854.
2
Behavioural effects of selective mu-, kappa-, and delta-opioid agonists in neonatal rats.
Psychopharmacology (Berl). 1989;97(3):404-9. doi: 10.1007/BF00439459.
3
CI-977, a novel and selective agonist for the kappa-opioid receptor.CI-977,一种新型的κ-阿片受体选择性激动剂。
Br J Pharmacol. 1990 Sep;101(1):183-9. doi: 10.1111/j.1476-5381.1990.tb12110.x.