Suppr超能文献

通过体内电化学方法在大鼠嗅结节中研究电诱发多巴胺释放的药理学。

Pharmacology of electrically evoked dopamine release studied in the rat olfactory tubercle by in vivo electrochemistry.

作者信息

Suaud-Chagny M F, Buda M, Gonon F G

机构信息

INSERM U 171-CNRS UA 1195, Centre Hospitalier Lyon Sud, Pierre-Bénite, France.

出版信息

Eur J Pharmacol. 1989 May 19;164(2):273-83. doi: 10.1016/0014-2999(89)90468-8.

Abstract

Dopamine (DA) release was evoked by electrical stimulation of the dopaminergic pathway. Electrically evoked DA release was monitored in the olfactory tubercle of anesthetized rats using differential pulse amperometry (DPA) combined with a treated carbon fiber electrode. Systemic injection of alpha-methyl-para-tyrosine (AMPT 250 mg/kg), NSD-1015 (50 mg/kg), reserpine (5 mg/kg), d,l-apomorphine (400 micrograms/kg) decreased evoked DA release while pargyline (75 mg/kg), nomifensine (4 and 20 mg/kg), methylphenidate (10 mg/kg), amphetamine (0.5, 2 and 5 mg/kg), sulpiride (20 mg/kg) and haloperidol (50 micrograms/kg) enhanced it. Thus, evoked DA release as measured indirectly by DPA is dependent upon synthesis, catabolism and vesicular processes. It can be also affected by DA releasers, DA re-uptake inhibitors, DA agonists and DA antagonists. These results suggest that under our experimental conditions all the drugs tested act directly on DA nerve terminals to modulate in vivo the evoked DA release.

摘要

通过电刺激多巴胺能通路诱发多巴胺(DA)释放。使用差分脉冲伏安法(DPA)结合经处理的碳纤维电极,在麻醉大鼠的嗅结节中监测电诱发的DA释放。全身注射α-甲基-对-酪氨酸(AMPT 250 mg/kg)、NSD-1015(50 mg/kg)、利血平(5 mg/kg)、d,l-阿扑吗啡(400 μg/kg)可降低诱发的DA释放,而帕吉林(75 mg/kg)、诺米芬辛(4和20 mg/kg)、哌醋甲酯(10 mg/kg)、苯丙胺(0.5、2和5 mg/kg)、舒必利(20 mg/kg)和氟哌啶醇(50 μg/kg)可增强其释放。因此,通过DPA间接测量的诱发DA释放取决于合成、分解代谢和囊泡过程。它也可受DA释放剂、DA再摄取抑制剂、DA激动剂和DA拮抗剂的影响。这些结果表明,在我们的实验条件下,所有测试药物均直接作用于DA神经末梢,以在体内调节诱发的DA释放。

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