钙通道阻滞剂硝苯地平和维拉帕米对小鼠焦虑影响的实验研究。

I G Fulga, V Stroescu
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引用次数: 0

摘要

采用条件抑制运动试验和黑白盒试验两种方法对钙通道阻滞剂硝苯地平和维拉帕米对小鼠的抗焦虑作用进行了研究。低剂量(0.1 mg/kg b.w)硝苯地平而非维拉帕米具有抗焦虑作用,高剂量(1.6 ~ 2.5 mg/kg b.w)硝苯地平和维拉帕米均具有致焦虑特性。焦虑效应与药物阻断钙通道的能力有关,低剂量硝苯地平的焦虑效应被认为是通过打开这些结构产生的。这些数据被认为对焦虑的治疗和病理生理学的新未来很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental research on the effect of calcium channel blockers nifedipine and verapamil on the anxiety in mice.

The anxiolytic effect of the calcium channel blockers nifedipine and verapamil was tested in mice using two test: the conditioned suppression of the motility test and the black and white box test. The nifedipine but not the verapamil, in low doses (0.1 mg/kg b.w), proved anxiolytic effect and both nifedipine and verapamil in high dose (1.6-2.5 mg/kg b.w) had anxiogenic properties. The anxiogenic effect was correlated with the capacity of the drugs to block the calcium channels and the anxiolytic effect of low doses of the nifedipine was considered to be produced by opening these structures. These data were considered important for a new future aboard of the treatment and pathophysiology of the anxiety.

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