• 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

[A comparative study of the neurochemical profiles of remoxipride, raclopride and metoclopramide activity].

作者信息

Gaĭnetdinov R R, Bogdanov M B, Kudrin V S, Budygin E A, Kovalev G I, Raevskiĭ K S

出版信息

Biull Eksp Biol Med. 1992 Jul;114(8):165-8.

PMID:1467481
Abstract

Effects of intraperitoneal administration of remoxipride (2.4 mg/kg), raclopride (1.2 mg/kg) and metoclopramide (5 mg/kg) on the concentration of monoamines and metabolites in various brain regions, on the DA and serotonin biosynthesis in the striatum and nucleus accumbens, on the K(+)-stimulated DA release from the isolated striatum, on the extracellular levels of DA and metabolites in the striatum of freely moving rats were studied. Remoxipride and raclopride increase DA turnover, biosynthesis and DA release, studied both in vitro and in vivo. Metoclopramide was shown to be more effective in increasing DA turnover and biosynthesis, while exerted less activity in regard to increasing DA release in vivo and failed to affect release in vitro. Possible neurochemical mechanisms underlying pharmacological effects of these drugs are discussed.

摘要

相似文献

1
[A comparative study of the neurochemical profiles of remoxipride, raclopride and metoclopramide activity].
Biull Eksp Biol Med. 1992 Jul;114(8):165-8.
2
Remoxipride and raclopride differ from metoclopramide by their effects on striatal dopamine release and biosynthesis in rats.
Neuropharmacology. 1994 Feb;33(2):215-9. doi: 10.1016/0028-3908(94)90011-6.
3
S 18126 ([2-[4-(2,3-dihydrobenzo[1,4]dioxin-6-yl)piperazin-1-yl methyl]indan-2-yl]), a potent, selective and competitive antagonist at dopamine D4 receptors: an in vitro and in vivo comparison with L 745,870 (3-(4-[4-chlorophenyl]piperazin-1-yl)methyl-1H-pyrrolo[2, 3b]pyridine) and raclopride.S 18126([2-[4-(2,3-二氢苯并[1,4]二噁英-6-基)哌嗪-1-基甲基]茚满-2-基]),一种强效、选择性且竞争性的多巴胺D4受体拮抗剂:与L 745,870(3-(4-[4-氯苯基]哌嗪-1-基)甲基-1H-吡咯并[2,3-b]吡啶)和雷氯必利的体外及体内比较
J Pharmacol Exp Ther. 1998 Oct;287(1):167-86.
4
[Different effects of typical and atypical neuroleptics on K+-stimulated dopamine release from isolated rat striatum].[典型和非典型抗精神病药物对离体大鼠纹状体中钾离子刺激的多巴胺释放的不同作用]
Biull Eksp Biol Med. 1992 Jul;114(7):47-9.
5
Remoxipride and raclopride differentially alter the activity of incertohypothalamic dopaminergic neurons.瑞莫必利和雷氯必利对未定带-下丘脑多巴胺能神经元的活性有不同影响。
Neuropharmacology. 1992 Nov;31(11):1121-6. doi: 10.1016/0028-3908(92)90008-d.
6
Comparison of the effects of remoxipride and raclopride on nigrostriatal and mesolimbic dopaminergic neuronal activity and on the secretion of prolactin and alpha-melanocyte-stimulating hormone.
Neuropsychopharmacology. 1992 Nov;7(3):205-11.
7
In vivo effects of remoxipride and aromatic ring metabolites in the rat.
J Pharmacol Exp Ther. 1997 Dec;283(3):1356-66.
8
S33084, a novel, potent, selective, and competitive antagonist at dopamine D(3)-receptors: I. Receptorial, electrophysiological and neurochemical profile compared with GR218,231 and L741,626.S33084,一种新型、强效、选择性且具有竞争性的多巴胺D(3)受体拮抗剂:I. 与GR218,231和L741,626相比的受体、电生理和神经化学特征
J Pharmacol Exp Ther. 2000 Jun;293(3):1048-62.
9
Day/night differences in D1 but not D2 DA receptor protection from EEDQ denaturation in rats treated with continuous cocaine.持续给予可卡因处理的大鼠中,D1而非D2多巴胺受体对EEDQ变性的昼夜差异。
Synapse. 1993 Jan;13(1):20-9. doi: 10.1002/syn.890130104.
10
Comparative dopamine-cholinergic mechanisms in the olfactory tubercle and the striatum: effects of metoclopramide.嗅结节和纹状体中多巴胺-胆碱能比较机制:胃复安的作用
J Pharmacol Exp Ther. 1987 Dec;243(3):840-51.