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钙通道拮抗剂氟桂利嗪的一些中枢药理作用。

Some central pharmacological effects of the calcium channel antagonist flunarizine.

作者信息

Czyrak A, Mogilnicka E, Maj J

机构信息

Institute of Pharmacology, Polish Academy of Sciences, Kraków.

出版信息

J Neural Transm Gen Sect. 1991;83(3):179-88. doi: 10.1007/BF01253388.

Abstract

Our earlier studies showed that dihydropyridine calcium channel antagonists have some central pharmacological effects. Flunarizine is considered to be a calcium channel antagonist; therefore this study was aimed at investigating the effect of flunarizine (given in single doses of 5, 10 and 20 mg/kg p.o.) in behavioural models in which calcium channel antagonists of the dihydropyridine type were previously studied. Flunarizine inhibited the apomorphine-induced stereotypy and yawning behaviour in rats. It decreased the hypothermia induced by a low dose of apomorphine in mice, but not that one induced by high dose of it. The quinpirole-induced hypothermia was also reduced. In the tests used for evaluation of the effect on the serotonergic system, flunarizine decreased the 5-HTP-induced head twitches and partly antagonized the fenfluramine- and quipazine-induced hyperthermias (at a high ambient temperature). In the forced swimming test flunarizine was inactive in mice and rats. The obtained results indicate that flunarizine exerts central antagonistic effects on the dopaminergic and serotonergic systems and has no antidepressant activity. Flunarizine differs from calcium channel antagonists of the dihydropyridine type, which have no dopamine-antagonistic activity and show anti-depressant-like properties.

摘要

我们早期的研究表明,二氢吡啶类钙通道拮抗剂具有一些中枢药理作用。氟桂利嗪被认为是一种钙通道拮抗剂;因此,本研究旨在研究氟桂利嗪(口服单剂量为5、10和20mg/kg)在先前研究过二氢吡啶类钙通道拮抗剂的行为模型中的作用。氟桂利嗪抑制大鼠阿扑吗啡诱导的刻板行为和打哈欠行为。它降低了低剂量阿扑吗啡诱导的小鼠体温过低,但对高剂量阿扑吗啡诱导的体温过低没有作用。喹吡罗诱导的体温过低也有所降低。在用于评估对血清素能系统影响的试验中,氟桂利嗪减少了5-羟色氨酸诱导的头部抽搐,并部分拮抗了芬氟拉明和喹哌嗪诱导的体温过高(在高环境温度下)。在强迫游泳试验中,氟桂利嗪对小鼠和大鼠均无活性。所得结果表明,氟桂利嗪对多巴胺能和血清素能系统发挥中枢拮抗作用,且无抗抑郁活性。氟桂利嗪与二氢吡啶类钙通道拮抗剂不同,后者没有多巴胺拮抗活性,且具有类抗抑郁特性。

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