Vinader-Caerols C., Brain P.F., Parra A., Simón V.M.
Area de Psicobiología, Facultad de Psicología, Universitat de València, Ap. 22109, 46071 Valencia, Spain.
Behav Pharmacol. 1992 Oct;3(5):427-433.
The effects of acutely administered benzodiazepines have largely been validated in male animals, in spite of the fact that the majority of anti-anxiety drugs are prescribed for female patients. A study was carried out assessing the potential of female mice in the testing of the anxiolytic properties of drugs. Three doses (0.5, 1.0 and 2.0mg/kg) of the benzodiazepines diazepam and nitrazepam were given to individually-housed female Swiss mice before dyadic encounters with anosmic, group-housed males. Videotape analysis of the encounters, using an ethopharmacological technique, revealed suppressive effects of diazepam (1.0 and 2.0mg/kg) and nitrazepam (all doses) on avoidance/flee, confirming the anxiolytic properties of these drugs. However, some doses of diazepam (2.0mg/kg) and nitrazepam (1.0mg/kg), greatly increased immobility with little effect on active behavioural elements. It is suggested that "immobility" does not simply measure sedation.
尽管大多数抗焦虑药物是开给女性患者的,但急性给予苯二氮䓬类药物的效果在雄性动物中已得到很大程度的验证。开展了一项研究,评估雌性小鼠在药物抗焦虑特性测试中的潜力。在单独饲养的雌性瑞士小鼠与嗅觉缺失、群居的雄性小鼠进行二元接触之前,给它们分别注射三种剂量(0.5、1.0和2.0毫克/千克)的苯二氮䓬类药物地西泮和硝西泮。使用行为药理学技术对接触过程进行录像分析,结果显示地西泮(1.0和2.0毫克/千克)和硝西泮(所有剂量)对回避/逃跑有抑制作用,证实了这些药物的抗焦虑特性。然而,某些剂量的地西泮(2.0毫克/千克)和硝西泮(1.0毫克/千克)会大大增加不动时间,而对主动行为成分影响很小。研究表明,“不动”不仅仅是对镇静作用的衡量。