Laboratory of Veterinary Ethology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Pharmacol Biochem Behav. 2010 Feb;94(4):575-9. doi: 10.1016/j.pbb.2009.11.013. Epub 2009 Dec 5.
Previously, we demonstrated that an alarm pheromone released from male donor Wistar rats evoked anxiety-related physiological and behavioral responses in recipient rats. Thus, we believe that this pheromone may increase anxiety levels in rats. In the current study, we evaluated the predictive validity of this alarm pheromone-induced anxiogenic effect in detail by investigating whether six types of human anxiolytics, each of which has a different mechanism of action, were efficacious in reducing anxiety, using changes in the acoustic startle reflex (ASR) as an index. The alarm pheromone-enhanced ASR was not affected by vehicle pretreatment but was dose-dependently attenuated by pretreatment with midazolam, phenelzine, propranolol, clonidine, and CP-154,526-although not buspirone. These results may reflect some aspects of the predictive validity of the alarm pheromone-induced anxiety in rats as an animal model of human anxiety.
先前,我们证明了雄性捐赠 Wistar 大鼠释放的报警信息素可引起接受大鼠的焦虑相关生理和行为反应。因此,我们认为这种信息素可能会增加大鼠的焦虑水平。在当前的研究中,我们通过研究六种不同作用机制的人用抗焦虑药是否能有效降低焦虑,以声音起始反射(ASR)的变化作为指标,详细评估了这种报警信息素引起的致焦虑作用的预测有效性。尽管没有苯并二氮䓬,但报警信息素增强的 ASR 不受载体预处理的影响,而是剂量依赖性地被咪达唑仑、苯乙肼、普萘洛尔、可乐定和 CP-154,526 减弱,而不是丁螺环酮。这些结果可能反映了大鼠报警信息素诱导的焦虑作为人类焦虑动物模型的预测有效性的某些方面。