Suppr超能文献

四氢氨基吖啶对大鼠脑内多巴胺和血清素摄取的抑制作用的表征

Characterisation of dopamine and serotonin uptake inhibitory effects of tetrahydroaminoacridine in rat brain.

作者信息

Jossan S S, Adem A, Winblad B, Oreland L

机构信息

Department of Medical Pharmacology, University of Uppsala, Sweden.

出版信息

Pharmacol Toxicol. 1992 Sep;71(3 Pt 1):213-5. doi: 10.1111/j.1600-0773.1992.tb00548.x.

Abstract

The effects of 1,2,3,4-tetrahydro-9-aminoacridine (THA) on uptake rates of radioactive 5-hydroxytryptamine (5-HT) and dopamine were investigated in rat diencephalon and striatal homogenates, respectively. Six and eight microM of THA were needed to inhibit 50% of dopamine and 5-HT uptake rates. Kinetic parameters, Km and Vmax, using six different concentrations of dopamine and 5-HT were estimated in the presence or absence of THA. A significant decrease in Vmax without any change in Km values was observed for both dopamine and 5-HT in the presence of THA. The results show that THA is a non-competitive uptake inhibitor of dopamine and 5-HT in the nerve terminals. The re-uptake blocking effect of THA on dopaminergic and serotonergic neurones, following THA treatment, might lead to increased levels of these monoamines in brains of Alzheimer patients and contribute in the therapeutic effects of the drug.

摘要

分别在大鼠间脑和纹状体匀浆中研究了1,2,3,4-四氢-9-氨基吖啶(THA)对放射性5-羟色胺(5-HT)和多巴胺摄取率的影响。抑制50%的多巴胺和5-HT摄取率分别需要6微摩尔和8微摩尔的THA。在有或没有THA的情况下,使用六种不同浓度的多巴胺和5-HT估计动力学参数Km和Vmax。在有THA的情况下,观察到多巴胺和5-HT的Vmax显著降低,而Km值没有任何变化。结果表明,THA是神经末梢中多巴胺和5-HT的非竞争性摄取抑制剂。THA治疗后对多巴胺能和血清素能神经元的再摄取阻断作用,可能会导致阿尔茨海默病患者大脑中这些单胺水平升高,并有助于该药物的治疗效果。

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