SOME CENTRAL PHARMACOLOGICAL EFFECTS OF THE CALCIUM-CHANNEL ANTAGONIST FLUNARIZINE

被引:22
作者
CZYRAK, A
MOGILNICKA, E
MAJ, J
机构
[1] Institute of Pharmacology, Polish Academy of Sciences, Kraków
关键词
DOPAMINE AND SEROTONIN; FLUNARIZINE - CENTRAL EFFECTS; MICE; RATS;
D O I
10.1007/BF01253388
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. Funarizine differs from calcium channel antagonists of the dihydropyridine type, which have no dopamine-antagonistic activity and show antidepressant-like properties.
引用
收藏
页码:179 / 188
页数:10
相关论文
共 26 条
[1]   VERAPAMIL AS AN APPARENT COMPETITIVE ANTAGONIST OF THE SEROTONIN RECEPTOR OF RABBIT ISOLATED AORTA [J].
AUGUET, M ;
DELAFLOTTE, S ;
CLOSTRE, F ;
DEFEUDIS, FV .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1986, 17 (02) :133-135
[2]   FLUNARIZINE INCREASES PRL SECRETION IN NORMAL AND IN MIGRAINEOUS WOMEN [J].
BONUCCELLI, U ;
PICCINI, P ;
PAOLETTI, AM ;
NUTI, A ;
COLZI, A ;
MELIS, GB ;
MURATORIO, A .
JOURNAL OF NEURAL TRANSMISSION, 1988, 74 (01) :43-53
[3]  
BORSINI F, 1988, PSYCHOPHARMACOLOGY, V94, P147
[4]  
CHOUZA C, 1986, LANCET, V1, P1303
[5]   A METHOD FOR ASSESSING EFFECTS OF DRUGS ON CENTRAL ACTIONS OF 5-HYDROXYTRYPTAMINE [J].
CORNE, SJ ;
WARNER, BT ;
PICKERING, RW .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1963, 20 (01) :106-&
[6]   POSSIBLE INVOLVEMENT OF A NORADRENERGIC AREA OF AMYGDALA WITH STEREOTYPED BEHAVIOR [J].
COSTALL, B ;
NAYLOR, RJ .
LIFE SCIENCE PART 1 PHYSIOLOGY & PHARMACOLOGY, 1972, 11 (24) :1135-&
[7]   SOME BEHAVIORAL-EFFECTS OF REPEATED ADMINISTRATION OF CALCIUM-CHANNEL ANTAGONISTS [J].
CZYRAK, A ;
MOGILNICKA, E ;
SIWANOWICZ, J ;
MAJ, J .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 35 (03) :557-560
[8]   DIHYDROPYRIDINE CALCIUM-CHANNEL ANTAGONISTS AS ANTIDEPRESSANT DRUGS IN MICE AND RATS [J].
CZYRAK, A ;
MOGILNICKA, E ;
MAJ, J .
NEUROPHARMACOLOGY, 1989, 28 (03) :229-233
[9]  
Di Chiara G, 1978, Adv Biochem Psychopharmacol, V19, P275
[10]   EFFECT OF DIFFERENT CA-2+ ENTRY BLOCKERS ON DOPAMINE-INDUCED INHIBITION OF INVITRO PROLACTIN SECRETION [J].
DIRENZO, G ;
AMOROSO, S ;
MAIDA, P ;
CANZONIERO, L ;
NAPPI, C ;
TAGLIALATELA, M ;
ANNUNZIA, L .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 146 (2-3) :201-206