Suppr超能文献

氟桂利嗪对[3H]多巴胺摄取的抑制作用。

Inhibition of [3H]dopamine uptake by flunarizine.

作者信息

Devoto P, Pani L, Kuzmin A, De Montis G

机构信息

Institute of Pharmacology and Biochemical Pathology, Cagliari, Italy.

出版信息

Eur J Pharmacol. 1991 Oct 2;203(1):67-9. doi: 10.1016/0014-2999(91)90791-n.

Abstract

The effect of different calcium channel blockers was studied on basal and cocaine-inhibited [3H]dopamine uptake in rat striatal synaptosomes. Isradipine (dihydropyridine calcium antagonist) and diltiazem (L-type calcium antagonist) were devoid of effect on [3H]dopamine uptake, while flunarizine (T-type calcium antagonist) inhibited [3H]dopamine uptake. Flunarizine inhibition was competitive and the inhibitory curve was biphasic with a Hill coefficient of 2.1. The high Hill number suggested a mechanism of positive cooperativity between two sites. Flunarizine inhibition showed a complex interaction with cocaine inhibition. While flunarizine at low concentrations interacts with a distinct site, at higher concentrations it interacts with the same site as cocaine. The relevance of this finding for the potentiation by flunarizine of cocaine-induced dopamine release in vivo is discussed.

摘要

研究了不同钙通道阻滞剂对大鼠纹状体突触体中基础及可卡因抑制的[3H]多巴胺摄取的影响。伊拉地平(二氢吡啶类钙拮抗剂)和地尔硫䓬(L型钙拮抗剂)对[3H]多巴胺摄取无影响,而氟桂利嗪(T型钙拮抗剂)抑制[3H]多巴胺摄取。氟桂利嗪的抑制作用具有竞争性,抑制曲线呈双相,希尔系数为2.1。较高的希尔系数表明两个位点之间存在正协同作用机制。氟桂利嗪的抑制作用与可卡因的抑制作用表现出复杂的相互作用。低浓度的氟桂利嗪与一个不同的位点相互作用,而高浓度时它与可卡因作用于相同的位点。讨论了这一发现与氟桂利嗪在体内增强可卡因诱导的多巴胺释放的相关性。

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