Cutler M G, Rodgers R J, Jackson J E
Department of Biological Sciences, Glasgow Caledonian University, UK.
Pharmacol Biochem Behav. 1997 Feb;56(2):287-93. doi: 10.1016/s0091-3057(96)00241-9.
In a continuation of recent work on effects of a benzodiazepine (chlordiazepoxide) and selective monoamine reuptake inhibitors (maprotiline and fluvoxamine), the current study compares effects of the 5-HT1A receptor partial agonist, buspirone (0.75-3.0 mg/kg), the 5-HT3 receptor antagonist, ondansetron (0.1-100 micrograms/kg) and the novel antidepressant, tianeptine (2.5-10.0 mg/kg). Compounds were given daily to mice for 21 days prior to testing and the subsequent behaviour of the animals during social interactions was assessed by ethopharmacological procedures. Buspirone, at 0.75 mg/kg, increased immobility and reduced occurrence of the aggressive act, "attack." At 1.5 and 3.0 mg/kg, it enhanced olfactory exploration of the sawdust substrate, but had no effect on social investigation. Ondansetron increased the duration of environmental exploration at 0.1 microgram/kg, while at 100 micrograms/kg it increased the duration of digging in the substrate. Ondansetron had no effect on the categories of behaviour and failed to induce an anxiolytic-like enhancement of social investigation. Tianeptine produced an anxiogenic-like effect at 10 mg/kg, while at 5 mg/kg it enhanced flight and immobility. The relevance of these findings is discussed in relation of the reported behavioural actions of these compounds and to current pharmacotherapy of anxiety and depression. The apparent anxiogenic effect of tianeptine is a novel finding which requires further study.
在最近关于苯二氮䓬类药物(氯氮卓)和选择性单胺再摄取抑制剂(马普替林和氟伏沙明)作用的研究基础上,本研究比较了5-HT1A受体部分激动剂丁螺环酮(0.75 - 3.0毫克/千克)、5-HT3受体拮抗剂昂丹司琼(0.1 - 100微克/千克)和新型抗抑郁药噻奈普汀(2.5 - 10.0毫克/千克)的作用。在测试前,每天给小鼠服用这些化合物,持续21天,然后通过行为药理学程序评估动物在社交互动中的后续行为。0.75毫克/千克的丁螺环酮增加了不动时间,并减少了攻击行为“攻击”的发生率。在1.5和3.0毫克/千克时,它增强了对锯末底物的嗅觉探索,但对社交探究没有影响。0.1微克/千克的昂丹司琼增加了环境探索的持续时间,而在100微克/千克时,它增加了在底物中挖掘的持续时间。昂丹司琼对行为类别没有影响,也没有诱导出类似抗焦虑的社交探究增强作用。10毫克/千克的噻奈普汀产生了类似致焦虑的作用,而在5毫克/千克时,它增强了逃避和不动行为。结合这些化合物已报道的行为作用以及当前焦虑和抑郁的药物治疗,对这些发现的相关性进行了讨论。噻奈普汀明显的致焦虑作用是一个新发现,需要进一步研究。