Suppr超能文献

5-羟色胺1(5-HT1)受体配体伊沙匹隆(TVX Q 7821)对小鼠和大鼠体内5-羟色胺合成的影响以及5-羟色胺激动剂的行为效应。

The effects of a 5-HT1 receptor ligand isapirone (TVX Q 7821) on 5-HT synthesis and the behavioural effects of 5-HT agonists in mice and rats.

作者信息

Goodwin G M, De Souza R J, Green A R

出版信息

Psychopharmacology (Berl). 1986;89(3):382-7. doi: 10.1007/BF00174379.

Abstract

The effects of 2-(4-(4-(2-pyrimidinyl)-1-piperazinyl)-butyl)-1,2-benzoisothiazol- 3(2H)one-1, 1-dioxide hydrochloride (isapirone, TVX Q 7821), a putative 5-HT1 receptor antagonist, has been studied on various models of 5-HT receptor sub-type function. In mice TVX Q 7821 produced a dose-dependent inhibition of the hypothermia induced by 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) with an ED50 of 5.3 mg/kg suggesting that TVX Q 7821 was an antagonist of the presynaptic (possibly somato-dendritic) 5-HT1A receptor. TVX Q 7821 did not alter the locomotor response to the suggested 5-HT1B agonist RU 24969. The rate of mouse brain 5-HT synthesis was accelerated by TVX Q 7821 (10 mg/kg). 5-HT2 receptor-mediated head twitch behaviour induced by precursor loading with 5-HTP was unaffected by TVX Q 7821 (10 mg/kg) pretreatment 75 min earlier, but the head-twitch induced by the agonist 5-methoxy-N,N-dimethyltryptamine was enhanced by prior treatment with TVX Q 7821. In rats the hypothermia induced by 8-OH-DPAT was partially antagonised by TVX Q 7821 while the behavioural "serotonin syndrome" induced by 8-OH-DPAT (a possible post-synaptic 5-HT1B-mediated effect) was unaffected by TVX Q 7821 as was the locomotion induced by RU 24969. The data suggest that TVX Q 7821 is a good presynaptic 5-HT1A antagonist in mice, as indicated by the 8-OH-DPAT-induced hypothermia and 5-HT synthesis rate studies. It did not antagonise 5-HT1B-mediated behaviour in mice or rats and appeared to have an antagonist action at pre- but not post-synaptic 5-HT1A receptors in rats.

摘要

2-(4-(4-(2-嘧啶基)-1-哌嗪基)-丁基)-1,2-苯并异噻唑-3(2H)酮-1,1-二氧化物盐酸盐(异哌隆,TVX Q 7821)是一种假定的5-羟色胺(5-HT)1受体拮抗剂,已在多种5-HT受体亚型功能模型上进行了研究。在小鼠中,TVX Q 7821对8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)诱导的体温过低产生剂量依赖性抑制,半数有效剂量(ED50)为5.3毫克/千克,这表明TVX Q 7821是突触前(可能是躯体-树突状)5-HT1A受体的拮抗剂。TVX Q 7821并未改变对假定的5-HT1B激动剂RU 24969的运动反应。TVX Q 7821(10毫克/千克)可加速小鼠脑内5-HT的合成。5-HT2受体介导的由5-羟色氨酸前体负荷诱导的头部抽搐行为,不受75分钟前TVX Q 7821(10毫克/千克)预处理的影响,但激动剂5-甲氧基-N,N-二甲基色胺诱导的头部抽搐可因预先用TVX Q 7821处理而增强。在大鼠中,TVX Q 7821可部分拮抗8-OH-DPAT诱导的体温过低,而8-OH-DPAT诱导的行为性“血清素综合征”(可能是突触后5-HT1B介导的效应)不受TVX Q 7821影响,RU 24969诱导的运动也不受影响。数据表明,如8-OH-DPAT诱导的体温过低和5-HT合成速率研究所显示,TVX Q 7821在小鼠中是一种良好的突触前5-HT1A拮抗剂。它在小鼠或大鼠中不拮抗5-HT1B介导的行为,并且在大鼠中似乎对突触前而非突触后5-HT1A受体具有拮抗作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验