Suppr超能文献

5-羟色胺(5-HT)1A受体激动剂氟西诺生对大鼠海马细胞外去甲肾上腺素水平及运动活性的影响。

Effect of a 5-HT(1A) receptor agonist, flesinoxan, on the extracellular noradrenaline level in the hippocampus and on the locomotor activity of rats.

作者信息

Suwabe A, Kubota M, Niwa M, Kobayashi K, Kanba S

机构信息

Department of Neuropsychiatry, Yamanashi Medical University, Shimokato 1110, Tamaho-cho, Yamanashi 409-3898, Japan.

出版信息

Brain Res. 2000 Mar 10;858(2):393-401. doi: 10.1016/s0006-8993(00)01941-7.

Abstract

We have studied effects of 5-hydroxytryptamine 1A (5-HT(1A)) receptor-selective compounds on the extracellular noradrenaline (NA) level in the hippocampus of rats using microdialysis and on their locomotor activity. A selective 5-HT(1A) receptor agonist, flesinoxan (5 mg/kg, i.p.) increased the extracellular NA level in the hippocampus, and increased the locomotor activity. Both responses were blocked by pretreatment with a 5-HT(1A) receptor antagonist, WAY100635 (1 mg/kg, i.p.) and an alpha(2) adrenoceptor agonist, clonidine (50 microg/kg, i.p.). Bilateral intrahippocampal injection of flesinoxan (200 nmol in 2 microl, respectively) increased the locomotor activity of rats and the intrahippocampal perfusion of flesinoxan (1 mM, 2 microl/min) increased the extracellular NA level in the hippocampus. Bilateral intrahippocampal injections of a small amount of WAY100635 (0.1 nmol in 2 microl, respectively) blocked the flesinoxan (5 mg/kg, i.p.)-induced hyperactivity. Flesinoxan (5 mg/kg, i.p.) did not significantly influence the level of serotonin or its major metabolite in the hippocampus, or dopamine or its metabolites in the striatum. In conclusion, these behavioral as well as pharmacological results indicate that postsynaptic 5-HT(1A) receptor activation by flesinoxan increase the extracellular NA level in the hippocampus, which may be the cause of the increase of the locomotor activity.

摘要

我们使用微透析技术研究了5-羟色胺1A(5-HT(1A))受体选择性化合物对大鼠海马细胞外去甲肾上腺素(NA)水平的影响及其对运动活性的影响。选择性5-HT(1A)受体激动剂氟司必林(5毫克/千克,腹腔注射)可提高海马细胞外NA水平,并增加运动活性。这两种反应均被5-HT(1A)受体拮抗剂WAY100635(1毫克/千克,腹腔注射)和α(2)肾上腺素能受体激动剂可乐定(50微克/千克,腹腔注射)预处理所阻断。双侧海马内注射氟司必林(分别为2微升中含200纳摩尔)可增加大鼠的运动活性,海马内灌注氟司必林(1毫摩尔,2微升/分钟)可提高海马细胞外NA水平。双侧海马内注射少量WAY100635(分别为2微升中含0.1纳摩尔)可阻断氟司必林(5毫克/千克,腹腔注射)诱导的多动。氟司必林(5毫克/千克,腹腔注射)对海马中5-羟色胺或其主要代谢产物水平,或纹状体中多巴胺或其代谢产物水平无显著影响。总之,这些行为学和药理学结果表明,氟司必林激活突触后5-HT(1A)受体可提高海马细胞外NA水平,这可能是运动活性增加的原因。

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