• 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

纳洛酮诱发的阿片类药物戒断部位与阿扑吗啡重新引发该现象的部位不同。

Site of naloxone-precipitated opiate withdrawal dissociates from that at which apomorphine reinitiates this phenomenon.

作者信息

Schulz R, Bläsig J, Laschka E, Herz A

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 Oct;305(1):1-4. doi: 10.1007/BF00496998.

DOI:10.1007/BF00496998
PMID:214718
Abstract

The site of action of naloxone to induce jumping in morphine tolerant/dependent rats appears to be dissociated from structures where apomorphine initiates its action to reinduce jumping in previously withdrawn animals. These findings suggest that dopaminergic pathways do not directly affect the neuronal circuit involved in withdrawal jumping behavior, but instead exert a facilitatory influence on neurons that become supersensitive during the state of withdrawal. Thus, an increased response to apomorphine during naloxone-precipitated opiate withdrawal does not necessarily imply a specific supersensitivity of the dopaminergic system.

摘要

纳洛酮诱导吗啡耐受/依赖大鼠跳跃的作用位点似乎与阿扑吗啡引发其作用以重新诱导先前戒断动物跳跃的结构无关。这些发现表明,多巴胺能通路并不直接影响参与戒断跳跃行为的神经回路,而是对在戒断状态下变得超敏的神经元发挥促进作用。因此,在纳洛酮诱发的阿片类药物戒断期间对阿扑吗啡反应增强并不一定意味着多巴胺能系统存在特定的超敏反应。

相似文献

1
Site of naloxone-precipitated opiate withdrawal dissociates from that at which apomorphine reinitiates this phenomenon.纳洛酮诱发的阿片类药物戒断部位与阿扑吗啡重新引发该现象的部位不同。
Naunyn Schmiedebergs Arch Pharmacol. 1978 Oct;305(1):1-4. doi: 10.1007/BF00496998.
2
Naloxone-precipitated withdrawal reveals sensitization to neurotransmitters in morphine tolerant/dependent rats.纳洛酮诱发的戒断反应揭示了吗啡耐受/依赖大鼠对神经递质的敏感性增强。
Naunyn Schmiedebergs Arch Pharmacol. 1977 Aug;299(1):95-9. doi: 10.1007/BF00508644.
3
Changes in sensitivity to apomorphine during morphine dependence and withdrawal in rats.大鼠吗啡依赖和戒断过程中对阿扑吗啡敏感性的变化。
J Pharmacol Exp Ther. 1976 Mar;196(3):637-41.
4
Dopaminergic influence on withdrawal jumping behavior in morphine-dependent mice.多巴胺能对吗啡依赖小鼠戒断跳跃行为的影响。
Res Commun Chem Pathol Pharmacol. 1976 Nov;15(3):435-46.
5
Paradoxical absence of aggression during naloxone-precipitated morphine withdrawal.纳洛酮诱发吗啡戒断期间出现矛盾性攻击行为缺失
Psychopharmacologia. 1975 Jul 23;43(1):43-6. doi: 10.1007/BF00437613.
6
Effects of intracerebroventricular clonidine on the hypothalamic noradrenaline and plasma corticosterone levels of opiate naive rats and after naloxone-induced withdrawal.脑室内注射可乐定对未使用阿片类药物大鼠及纳洛酮诱导戒断后大鼠下丘脑去甲肾上腺素和血浆皮质酮水平的影响
Brain Res. 1994 Jun 6;647(2):199-203. doi: 10.1016/0006-8993(94)91318-8.
7
Evidence of a preferential role of brain serotonin in the mechanisms leading to naloxone-precipitated compulsive jumping in morphine-dependent rats.脑血清素在吗啡依赖大鼠中导致纳洛酮诱发强迫性跳跃的机制中起优先作用的证据。
Psychopharmacology (Berl). 1981;74(3):271-4. doi: 10.1007/BF00427109.
8
Modification of the development of acute opiate tolerance by increased dopamine receptor sensitivity.通过增加多巴胺受体敏感性对急性阿片类药物耐受性发展的修饰。
J Pharmacol Exp Ther. 1987 Apr;241(1):48-55.
9
Dorsal and median raphe serotonergic system lesion does not alter the opiate withdrawal syndrome.背侧和中缝5-羟色胺能系统损伤不会改变阿片类药物戒断综合征。
Pharmacol Biochem Behav. 2002 Jul;72(4):979-86. doi: 10.1016/s0091-3057(02)00810-9.
10
Central sites of naloxone-precipitated shaking in the anesthetized, morphine-dependent rat.纳洛酮诱发麻醉吗啡依赖大鼠颤抖的中枢部位
J Pharmacol Exp Ther. 1975 Dec;195(3):480-7.

引用本文的文献

1
The effects of thyrotropin-releasing hormone on the central nervous system responses to chronic morphine administration.促甲状腺激素释放激素对慢性给予吗啡后中枢神经系统反应的影响。
Psychopharmacology (Berl). 1980;68(2):185-9. doi: 10.1007/BF00432139.
2
Jumping behavior induced by thyrotropin releasing hormone in combination with apomorphine in mice.促甲状腺激素释放激素与阿扑吗啡联合诱导小鼠的跳跃行为。
Psychopharmacology (Berl). 1982;76(1):1-4. doi: 10.1007/BF00430745.

本文引用的文献

1
A GENERAL THEORY OF THE GENESIS OF DRUG DEPENDENCE BY INDUCTION OF RECEPTORS.通过诱导受体产生药物依赖性的一般理论。
Nature. 1965 Jan 9;205:181-2. doi: 10.1038/205181a0.
2
XVII. Pharmacological denervation supersensitivity in the central nervous system: a theory of physical dependence.十七、中枢神经系统中的药理去神经超敏反应:一种身体依赖理论。
Res Publ Assoc Res Nerv Ment Dis. 1968;46:226-46.
3
Development of physical dependence on morphine in respect to time and dosage and quantification of the precipitated withdrawal syndrome in rats.
大鼠对吗啡身体依赖性的发展与时间、剂量的关系以及戒断综合征的量化
Psychopharmacologia. 1973 Oct 23;33(1):19-38. doi: 10.1007/BF00428791.
4
Morphine abstinence syndrome in rabbits precipitated by injection of morphine antagonists into the ventricular system and restricted parts of it.通过向家兔脑室系统及其受限部分注射吗啡拮抗剂诱发的吗啡戒断综合征。
Psychopharmacologia. 1972;26(3):219-35. doi: 10.1007/BF00422698.
5
Central sites of naloxone-precipitated shaking in the anesthetized, morphine-dependent rat.纳洛酮诱发麻醉吗啡依赖大鼠颤抖的中枢部位
J Pharmacol Exp Ther. 1975 Dec;195(3):480-7.
6
Aspects of opiate dependence in the myenteric plexus of the guinea-pig.
Life Sci. 1976 Oct 15;19(8):1117-27. doi: 10.1016/0024-3205(76)90246-0.
7
The role of dopamine in withdrawal jumping in morphine dependent rats.多巴胺在吗啡依赖大鼠戒断跳跃中的作用。
Arzneimittelforschung. 1976;26(6):1104-6.
8
Sites of action of morphine involved in the development of physical dependence in rats. II. Morphine withdrawal precipitated by application of morphine antagonists into restricted parts of the ventricular system and by microinjection into various brain areas.
Psychopharmacologia. 1976 Mar 16;46(2):141-7. doi: 10.1007/BF00421383.
9
Opiate tolerance and dependence induced in vitro in single myenteric neurones.阿片类药物耐受性和依赖性在离体单个肠肌间神经元中的诱导
Nature. 1978 Mar 2;272(5648):73-5. doi: 10.1038/272073a0.
10
Sites of action of morphine involved in the development of physical dependence in rats. III. Autoradiographic studies.吗啡在大鼠身体依赖性形成过程中的作用位点。III. 放射自显影研究。
Psychopharmacology (Berl). 1977 Jun 6;53(1):33-7. doi: 10.1007/BF00426691.