• 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

Relative effectiveness of pimozide, haloperidol and trifluoperazine on self-stimulation rate-intensity functions.

作者信息

Lynch M R, Wise R A

出版信息

Pharmacol Biochem Behav. 1985 Nov;23(5):777-80. doi: 10.1016/0091-3057(85)90071-1.

DOI:10.1016/0091-3057(85)90071-1
PMID:4080763
Abstract

Rats were trained to lever press for 60 Hz sine wave stimulation of the medial forebrain bundle (MFB) at the level of the lateral hypothalamus. Rate intensity functions were determined by stepping down the current intensity by 0.05 log10 units every five min. Haloperidol shifted the function approximately one step to the right at 0.08 mg/kg, with lower doses producing no effect. Pimozide shifted the curve in a dose-dependent manner over the range of 0.06 to 0.24 mg/kg; 0.12 mg/kg produced an approximate one-step shift. Trifluoperazine also produced dose related shifts to the right over the range of 0.08 to 0.32 mg/kg; this agent, unlike the others, appeared to shift the curve down as well as to the right. Less than a one-step shift was produced by 0.08 mg/kg; more than a one-step shift was produced by 0.16 mg/kg. On a molar basis, the order of potency for displacing the curves to the right was haloperidol, pimozide and trifluoperazine. While this order of potency is not predicted from simple in vitro binding affinities for the D2 receptor, this may be due to differences in the penetration of these agents to central D2 receptors in vivo.

摘要

相似文献

1
Relative effectiveness of pimozide, haloperidol and trifluoperazine on self-stimulation rate-intensity functions.
Pharmacol Biochem Behav. 1985 Nov;23(5):777-80. doi: 10.1016/0091-3057(85)90071-1.
2
Dose-response functions of apomorphine, SKF 38393, LY 171555, haloperidol and clonidine on the self-stimulation evoked from lateral hypothalamus and ventral tegmentum.阿扑吗啡、SKF 38393、LY 171555、氟哌啶醇和可乐定对下丘脑外侧区和腹侧被盖区诱发的自我刺激的剂量反应函数。
Indian J Physiol Pharmacol. 1996 Jan;40(1):15-22.
3
The effects of dexetimide on pimozide-, haloperidol- and pipamperone-induced inhibition of brain self-stimulation in rats.右苄替米特对匹莫齐特、氟哌啶醇和哌泊噻嗪诱导的大鼠脑自我刺激抑制作用的影响。
Arch Int Pharmacodyn Ther. 1975 Oct;217(2):280-92.
4
Effects of dopamine supersensitivity on lateral hypothalamic self-stimulation in rats.多巴胺超敏对大鼠下丘脑外侧自我刺激的影响。
Pharmacol Biochem Behav. 1977 Dec;7(6):507-14. doi: 10.1016/0091-3057(77)90246-5.
5
Intracranial self-stimulation in rats as a function of various stimulus parameters. II. Influence of haloperidol, pimozide and pipamperone on medial forebrain bundle stimulation with monopolar electrodes.大鼠颅内自我刺激与各种刺激参数的关系。II. 氟哌啶醇、匹莫齐特和哌泊噻嗪对单极电极刺激内侧前脑束的影响。
Psychopharmacologia. 1972;27(3):191-202. doi: 10.1007/BF00422799.
6
The curve-shift paradigm in self-stimulation.自我刺激中的曲线偏移范式。
Physiol Behav. 1986;37(1):85-91. doi: 10.1016/0031-9384(86)90388-4.
7
Decreased intracranial self-stimulation after neuroleptics or 6-hydroxydopamine: evidence for mediation by motor deficits rather than by reduced reward.使用抗精神病药物或6-羟基多巴胺后颅内自我刺激减少:运动功能缺陷而非奖励减少介导的证据。
Psychopharmacology (Berl). 1976 May 5;47(1):21-7. doi: 10.1007/BF00428696.
8
Free-operant and auto-titration brain self-stimulation procedures in the rat: a comparison of drug effects.大鼠自由操作和自动滴定脑自我刺激程序:药物效应比较
Pharmacol Biochem Behav. 1979 Jan;10(1):127-35. doi: 10.1016/0091-3057(79)90178-3.
9
Acute effects of neuroleptics on brain self-stimulation thresholds in rats.抗精神病药物对大鼠脑自我刺激阈值的急性影响。
Psychopharmacology (Berl). 1980 Jan;67(1):9-15. doi: 10.1007/BF00427589.
10
Differential effects of pimozide on response-rate and choice accuracy in a self-stimulation paradigm in mice.匹莫齐特对小鼠自我刺激范式中反应率和选择准确性的差异影响。
Pharmacol Biochem Behav. 1985 Apr;22(4):521-6. doi: 10.1016/0091-3057(85)90268-0.

引用本文的文献

1
Using rodent data to elucidate dopaminergic mechanisms of ADHD: Implications for human personality.利用啮齿动物数据阐明注意力缺陷多动障碍的多巴胺能机制:对人类个性的影响。
Personal Neurosci. 2024 Jan 31;7:e2. doi: 10.1017/pen.2023.12. eCollection 2024.
2
Behavioural effects in the rat of the putative dopamine D3 receptor agonist 7-OH-DPAT: comparison with quinpirole and apomorphine.假定的多巴胺D3受体激动剂7-羟基-DPAT对大鼠的行为影响:与喹吡罗和阿扑吗啡的比较。
Psychopharmacology (Berl). 1996 Apr;124(3):231-40. doi: 10.1007/BF02246662.
3
Striatal dopamine in motor activation and reward-mediated learning: steps towards a unifying model.
纹状体多巴胺在运动激活和奖赏介导的学习中的作用:迈向统一模型的步骤
J Neural Transm Gen Sect. 1990;80(1):9-31. doi: 10.1007/BF01245020.
4
Chronic low-dose haloperidol effects on self-stimulation rate-intensity functions.慢性低剂量氟哌啶醇对自我刺激速率-强度函数的影响。
Psychopharmacology (Berl). 1990;102(1):122-9. doi: 10.1007/BF02245756.