Czarnecka E, Tymczyszyn W
Department of Pharmacology, Medical Academy, Lódź, Poland.
Pol J Pharmacol. 1994 May-Jun;46(3):125-31.
The influence of verapamil, nifedipine and cinnarizine on clonidine-induced hypothermia, spontaneous and explorative motility was investigated in mice. Verapamil 5 and 15 mg/kg, nifedipine 17.5 and 50 mg/kg and cinnarizine 75 and 200 mg/kg (that is 1/30 and 1/10 of LD50 respectively) were injected intraperitoneally. The drugs were given in single doses (1/10 LD50) and in repeated doses (1/30 LD50) during a 10 days course. In acute experiments the drugs were given 60 min before clonidine administration, while in chronic experiments clonidine was given on the 11th day of the experiment. Nifedipine prevents clonidine-induced hypothermia in both the applied doses, verapamil only in a single dose, and cinnarizine in repeated doses. Only repeated administration of nifedipine and cinnarizine weakens the clonidine-induced sedation in the studies of spontaneous motility, and as for nifedipine also in explorative motility.
研究了维拉帕米、硝苯地平和桂利嗪对小鼠可乐定诱导的体温过低、自发活动和探究性活动的影响。腹腔注射维拉帕米5毫克/千克和15毫克/千克、硝苯地平17.5毫克/千克和50毫克/千克以及桂利嗪75毫克/千克和200毫克/千克(分别为半数致死量的1/30和1/10)。药物以单次剂量(1/10半数致死量)和重复剂量(1/30半数致死量)给药,疗程为10天。在急性实验中,药物在给予可乐定前60分钟给药,而在慢性实验中,可乐定在实验的第11天给药。硝苯地平在两种给药剂量下均能预防可乐定诱导的体温过低,维拉帕米仅在单次给药时有效,桂利嗪在重复给药时有效。在自发活动研究中,只有重复给予硝苯地平和桂利嗪会减弱可乐定诱导的镇静作用,而对于硝苯地平,在探究性活动研究中也是如此。