Talalaenko A N, Kharin N A
Eksp Klin Farmakol. 1993 Mar-Apr;56(2):11-3.
1-(2-pyrimidinyl)-piperazine derivatives (ipsapirone and campirone) injected intraperitoneally or into dorsalis nucleus raphe and dorsalis hippocampus of rats revealed dose-dependent anxiolytic action in avoidance procedure and conflict situations. 5-HT locally injected into the nucleus raphe and hippocampus revealed a role of serotoninergic mechanisms of these brain formations in the studied anxiety conditions of different aversive genesis. It is concluded that anxiolytic effect dissociation revealed in different anxiety tests, are stipulated by serotonin and its agonists due to nucleus raphe and hippocampus chemical stimulation my suggest their different neurochemical contribution and nonserotoninergic component involved in the mechanism of 1-(2-pyrimidinyl)-piperazine derivative anxiolytic action.
腹腔注射或注入大鼠中缝背核和背侧海马的1-(2-嘧啶基)-哌嗪衍生物(伊沙匹隆和坎匹隆)在回避程序和冲突情境中显示出剂量依赖性抗焦虑作用。局部注射到中缝核和海马的5-羟色胺揭示了这些脑区的5-羟色胺能机制在不同厌恶起源的研究焦虑状态中的作用。得出的结论是,在不同焦虑测试中揭示的抗焦虑作用解离是由5-羟色胺及其激动剂引起的,因为中缝核和海马的化学刺激表明它们有不同的神经化学贡献,且非5-羟色胺能成分参与了1-(2-嘧啶基)-哌嗪衍生物抗焦虑作用机制。