• 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

5-HT3 receptor antagonist MDL 72222 dose-dependently attenuates cocaine- and amphetamine-induced elevations of extracellular dopamine in the nucleus accumbens and the dorsal striatum.

作者信息

Kankaanpää A, Lillsunde P, Ruotsalainen M, Ahtee L, Seppâlä T

机构信息

National Public Health Institute, Laboratory of Pharmacology and Toxicology, Helsinki, Finland.

出版信息

Pharmacol Toxicol. 1996 May;78(5):317-21. doi: 10.1111/j.1600-0773.1996.tb01382.x.

DOI:10.1111/j.1600-0773.1996.tb01382.x
PMID:8737967
Abstract

The effects of a 5-HT3 receptor antagonist MDL 72222 on cocaine- and amphetamine-induced increases in extracellular dopamine in the nucleus accumbens and the dorsal striatum were studied with microdialysis technique using halothane anaesthesized rats. Dopamine and its metabolites were measured by HPLC with electrochemical detection. Cocaine elevated extracellular dopamine in the nucleus accumbens and to a lesser extent in the dorsal striatum, but it did not affect dopamine metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid. Pretreatment with MDL 72222 (25-100 micrograms/kg) dose-dependently attenuated cocaine-induced elevation of dopamine in both of the nuclei studied. Amphetamine elevated extracellular dopamine and reduced DOPAC and homovanillic acid equally in the nucleus accumbens and in the dorsal striatum. MDL 72222 also attenuated the amphetamine-induced elevation of extracellular dopamine concentration in both brain areas studied, but first at a dose of 100 micrograms/kg. The different potencies of the interactions of the 5-HT3 receptor antagonist with cocaine and amphetamine could be related to the different mechanisms by which these drugs primarily elevate extracellular dopamine.

摘要

相似文献

1
5-HT3 receptor antagonist MDL 72222 dose-dependently attenuates cocaine- and amphetamine-induced elevations of extracellular dopamine in the nucleus accumbens and the dorsal striatum.
Pharmacol Toxicol. 1996 May;78(5):317-21. doi: 10.1111/j.1600-0773.1996.tb01382.x.
2
5-HT3 receptor antagonist MDL 72222 attenuates cocaine- and mazindol-, but not methylphenidate-induced neurochemical and behavioral effects in the rat.5-羟色胺3受体拮抗剂MDL 72222可减弱可卡因和吗茚酮对大鼠的神经化学及行为学影响,但对哌甲酯无此作用。
Psychopharmacology (Berl). 2002 Feb;159(4):341-50. doi: 10.1007/s00213-001-0939-4. Epub 2001 Nov 23.
3
Naloxone reduces the neurochemical and behavioral effects of amphetamine but not those of cocaine.纳洛酮可减轻苯丙胺的神经化学和行为效应,但对可卡因则无此作用。
Eur J Pharmacol. 1995 Feb 24;275(1):9-16. doi: 10.1016/0014-2999(94)00726-n.
4
Effects of repeated daily treatments with a 5-HT3 receptor antagonist on dopamine neurotransmission and functional activity of 5-HT3 receptors within the nucleus accumbens of Wistar rats.5-羟色胺3受体拮抗剂每日重复给药对Wistar大鼠伏隔核内多巴胺神经传递及5-羟色胺3受体功能活性的影响。
Pharmacol Biochem Behav. 2006 Jun;84(2):370-7. doi: 10.1016/j.pbb.2006.06.002. Epub 2006 Jul 7.
5
Simultaneous microdialysis and amphetamine infusion in the nucleus accumbens and striatum of freely moving rats: increase in extracellular dopamine and serotonin.在自由活动大鼠的伏隔核和纹状体中同时进行微透析和注入苯丙胺:细胞外多巴胺和5-羟色胺增加。
Brain Res Bull. 1987 Dec;19(6):623-8. doi: 10.1016/0361-9230(87)90047-5.
6
The 5-HT1A receptor antagonist (S)-UH-301 decreases dopamine release in the rat nucleus accumbens and striatum.5-羟色胺1A受体拮抗剂(S)-UH-301可降低大鼠伏隔核和纹状体中的多巴胺释放。
J Neural Transm (Vienna). 1996;103(5):541-54. doi: 10.1007/BF01273152.
7
Antagonism of 5-HT3 receptors attenuates the effects of ethanol on extracellular dopamine.5-羟色胺3受体的拮抗作用可减弱乙醇对细胞外多巴胺的影响。
Eur J Pharmacol. 1990 Oct 9;187(2):287-9. doi: 10.1016/0014-2999(90)90015-x.
8
5-HT3 receptor antagonists do not modify cocaine place conditioning or the rise in extracellular dopamine in the nucleus accumbens of rats.5-羟色胺3受体拮抗剂不会改变可卡因引起的条件性位置偏爱,也不会改变大鼠伏隔核细胞外多巴胺水平的升高。
Pharmacol Biochem Behav. 1996 Sep;55(1):33-7. doi: 10.1016/0091-3057(96)00046-9.
9
5-HT3 receptor agonist induced carrier-mediated release of dopamine in rat striatum in vivo.5-羟色胺3受体激动剂在体内诱导大鼠纹状体中多巴胺的载体介导释放。
Br J Pharmacol. 1995 Sep;116(1):1545-50. doi: 10.1111/j.1476-5381.1995.tb16371.x.
10
5-HT(6) receptor antagonism potentiates the behavioral and neurochemical effects of amphetamine but not cocaine.5-羟色胺(6)受体拮抗作用增强了苯丙胺的行为和神经化学效应,但对可卡因则无此作用。
Neuropharmacology. 2002 Feb;42(2):170-80. doi: 10.1016/s0028-3908(01)00165-4.

引用本文的文献

1
A randomized, double-blind, placebo-controlled trial of ondansetron for the treatment of cocaine use disorder with post hoc pharmacogenetic analysis.一项关于昂丹司琼治疗可卡因使用障碍的随机、双盲、安慰剂对照试验,事后进行了基于药理学的遗传分析。
Drug Alcohol Depend. 2021 Nov 1;228:109074. doi: 10.1016/j.drugalcdep.2021.109074. Epub 2021 Sep 24.
2
Contrasting effects of 5-HT receptor stimulation of the nucleus accumbens or ventral tegmentum on food intake in the rat.伏隔核或腹侧被盖区5-羟色胺受体刺激对大鼠食物摄入的对比作用。
Behav Brain Res. 2017 Apr 14;323:15-23. doi: 10.1016/j.bbr.2017.01.031. Epub 2017 Jan 20.
3
Role of serotonin in central dopamine dysfunction.
血清素在中枢多巴胺功能障碍中的作用。
CNS Neurosci Ther. 2010 Jun;16(3):179-94. doi: 10.1111/j.1755-5949.2010.00135.x.
4
Activation of 5-HT3 receptors leads to altered responses 6 months after MDMA treatment.5-HT3 受体的激活导致 MDMA 治疗 6 个月后反应改变。
J Neural Transm (Vienna). 2010 Mar;117(3):285-92. doi: 10.1007/s00702-009-0357-z. Epub 2010 Jan 6.
5
Enhanced locomotor, reinforcing, and neurochemical effects of cocaine in serotonin 5-hydroxytryptamine 2C receptor mutant mice.可卡因对血清素5-羟色胺2C受体突变小鼠的运动、强化及神经化学作用增强。
J Neurosci. 2002 Nov 15;22(22):10039-45. doi: 10.1523/JNEUROSCI.22-22-10039.2002.
6
Involvement of 5-HT(3) receptors in the nucleus accumbens in the potentiation of cocaine-induced behaviours in the rat.伏隔核中5-羟色胺(3)受体参与可卡因诱导的大鼠行为增强作用。
Br J Pharmacol. 2000 Dec;131(7):1294-302. doi: 10.1038/sj.bjp.0703687.