• 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

Postsynaptic receptors are not essential for dopaminergic feedback regulation.

作者信息

Di Chiara G, Porceddu M L, Fratta W, Gessa G L

出版信息

Nature. 1977 May 19;267(5608):270-2. doi: 10.1038/267270a0.

DOI:10.1038/267270a0
PMID:865621
Abstract
摘要

相似文献

1
Postsynaptic receptors are not essential for dopaminergic feedback regulation.突触后受体对于多巴胺能反馈调节并非必不可少。
Nature. 1977 May 19;267(5608):270-2. doi: 10.1038/267270a0.
2
Haloperidol increases and apomorphine decreases striatal dopamine metabolism after destruction of striatal dopamine-sensitive adenylate cyclase by kainic acid.在纹状体多巴胺敏感的腺苷酸环化酶被海人酸破坏后，氟哌啶醇会增加而阿扑吗啡会降低纹状体多巴胺代谢。
Brain Res. 1977 Jul 15;130(2):374-82. doi: 10.1016/0006-8993(77)90286-4.
3
Developmental change in striatal concentration of homovanillic acid and 3,4-dihydroxyphenylacetic acid in response to apomorphine and haloperidol treatment.对阿扑吗啡和氟哌啶醇治疗的反应中，纹状体内高香草酸和3,4-二羟基苯乙酸浓度的发育变化。
Arch Int Pharmacodyn Ther. 1979 Jan;237(1):25-30.
4
[Effect of intracaudate administration of kainic acid on the activity of the dopaminergic system].[尾状核内注射 kainic 酸对多巴胺能系统活性的影响]
Fiziol Zh SSSR Im I M Sechenova. 1981 Nov;67(11):1606-10.
5
Apomorphine-haloperidol interactions: different types of antagonism in cortical and subcortical brain regions.阿扑吗啡-氟哌啶醇相互作用：皮质和皮质下脑区不同类型的拮抗作用。
Brain Res. 1981 Feb 2;205(2):313-9. doi: 10.1016/0006-8993(81)90342-5.
6
Haloperidol prevents the methamphetamine-induced apomorphine subsensitivity of dopamine metabolism in rat striatum.
Neurosci Res. 1987 Jun;4(5):428-32. doi: 10.1016/0168-0102(87)90009-5.
7
Lithium dissociates haloperidol-induced behavioral supersensitivity from reduced dopac increase in rat striatum.锂可使大鼠纹状体中氟哌啶醇诱导的行为超敏反应与多巴胺代谢产物二羟基苯乙酸（DOPAC）增加的减少相分离。
Eur J Pharmacol. 1981 Nov 19;76(1):25-9. doi: 10.1016/0014-2999(81)90005-4.
8
Striatal dopamine receptors become supersensitive while rats are geven trifluoperazine for six months.当给大鼠服用三氟拉嗪六个月时，纹状体多巴胺受体会变得超敏。
Nature. 1979 Mar 1;278(5699):59-61. doi: 10.1038/278059a0.
9
Dopaminergic receptor activity in substantia nigra in the mechanisms of autoregulation of striatal dopamine release.黑质中多巴胺能受体活性在纹状体多巴胺释放的自动调节机制中所起的作用。
Adv Biochem Psychopharmacol. 1978;19:363-71.
10
Haloperidol inhibits the disappearance of acidic dopamine metabolites from rat striatum.
J Pharm Pharmacol. 1978 Sep;30(9):583-5. doi: 10.1111/j.2042-7158.1978.tb13330.x.

引用本文的文献

1
Disruption of positive- and negative-feature morphine interoceptive occasion setters by dopamine receptor agonism and antagonism in male and female rats.多巴胺受体激动剂和拮抗剂对雄性和雌性大鼠正性和负性吗啡内感受触发特征的干扰。
Psychopharmacology (Berl). 2024 Aug;241(8):1597-1615. doi: 10.1007/s00213-024-06584-y. Epub 2024 Apr 6.
2
An Introspective Approach: A Lifetime of Parkinson's Disease Research and Not Much to Show for it Yet?内省的方法：一生的帕金森病研究，却还没有太多成果？
Cells. 2021 Feb 28;10(3):513. doi: 10.3390/cells10030513.
3
Residual dopamine receptor desensitization following either high- or low-dose sub-chronic prior exposure to the atypical anti-psychotic drug olanzapine.
无论是高剂量还是低剂量的亚慢性预先暴露于非典型抗精神病药物奥氮平后，残留多巴胺受体脱敏。
Psychopharmacology (Berl). 2013 Jan;225(1):141-50. doi: 10.1007/s00213-012-2802-1. Epub 2012 Jul 24.
4
Memory re-consolidation and drug conditioning: an apomorphine conditioned locomotor stimulant response can be enhanced or reversed by a single high versus low apomorphine post-trial treatment.记忆再巩固和药物条件作用：单次高剂量 versus 低剂量阿朴吗啡（apomorphine）试验后处理可增强或逆转阿朴吗啡条件性运动刺激反应。
Psychopharmacology (Berl). 2012 Mar;220(2):281-91. doi: 10.1007/s00213-011-2474-2. Epub 2011 Sep 16.
5
Effect of low concentrations of apomorphine on parkinsonism in a randomized, placebo-controlled, crossover study.低浓度阿扑吗啡对帕金森病影响的随机、安慰剂对照、交叉研究
Arch Neurol. 2008 Feb;65(2):193-8. doi: 10.1001/archneurol.2007.58.
6
The 5-HT1A receptor and behavioral stimulation in the rat: effects of 8-OHDPAT on spontaneous and cocaine-induced behavior.5-羟色胺1A受体与大鼠的行为刺激：8-羟基二苯丙氨酸对自发行为和可卡因诱导行为的影响。
Psychopharmacology (Berl). 2004 Dec;177(1-2):46-54. doi: 10.1007/s00213-004-1917-4. Epub 2004 May 28.
7
A comparison of the potencies of various dopamine receptor agonists in models for pre- and postsynaptic receptor activity.
Naunyn Schmiedebergs Arch Pharmacol. 1983 Sep;324(2):108-15. doi: 10.1007/BF00497015.
8
Disinhibitory effects of buspirone and low doses of sulpiride and haloperidol in two experimental anxiety models in rats: possible role of dopamine.丁螺环酮以及低剂量舒必利和氟哌啶醇在大鼠的两种实验性焦虑模型中的去抑制作用：多巴胺的可能作用
Psychopharmacology (Berl). 1986;89(1):125-30. doi: 10.1007/BF00175204.
9
Effects of D-2 agonists on the release of dopamine: localization of the mechanism of action.
Naunyn Schmiedebergs Arch Pharmacol. 1990 Dec;342(6):650-4. doi: 10.1007/BF00175707.
10
Evidence for selective and long-lasting stimulation of "regulatory" dopamine-receptors by bromocriptine (CB 154).溴隐亭（CB 154）对“调节性”多巴胺受体进行选择性和长效刺激的证据。
Naunyn Schmiedebergs Arch Pharmacol. 1977 Nov;300(3):239-45. doi: 10.1007/BF00500966.