Kozlovskiĭ V L, Prakh'e I V
Eksp Klin Farmakol. 1995 Jan-Feb;58(1):18-20.
The anxiolytic activity of calcium channel blockers (verapamil, nifedipine, cinnarizine, fendiline, and diltiazem) versus diazepam (relanium) was tested in experiments on male [correction of female] mice. Only verapamil (1 mg/kg) and nifedipine (5 mg/kg) were found to increase the number of transitions and reduced the animals' stay in the dark compartment. All the agents in the used doses failed to substantially affect the animals' behavior in the plus-maze. It is suggested that conditions for modelling pathological anxiety rather than natural states are required in the experiments where antianxiety properties are studied. The model of pathological anxiety states is possible in the examination of the action of agents on the effects of routine anxiogenic agents.
在雄性[纠正为雌性]小鼠实验中测试了钙通道阻滞剂(维拉帕米、硝苯地平、桂利嗪、芬地林和地尔硫䓬)与地西泮(安定)相比的抗焦虑活性。仅发现维拉帕米(1毫克/千克)和硝苯地平(5毫克/千克)能增加穿梭次数并减少动物在暗室中的停留时间。所用剂量的所有药物均未对动物在十字迷宫中的行为产生实质性影响。建议在研究抗焦虑特性的实验中,需要模拟病理性焦虑而非自然状态的条件。在研究药物对常规致焦虑剂作用的影响时,病理性焦虑状态模型是可行的。