Engel Odilo, Masic Aleksandar, Landsberg Gary, Brooks Melissa, Mills Daniel S, Rundfeldt Chris
Boehringer Ingelheim Vetmedica GmbH, Ingelheim am Rhein, Germany.
CanCog Technologies Inc., Toronto, ON, Canada.
Front Pharmacol. 2018 Nov 1;9:1225. doi: 10.3389/fphar.2018.01225. eCollection 2018.
Imepitoin is a low affinity partial agonist for the benzodiazepine binding site of γ-aminobutyric acid (GABA) receptors, and is currently used as an antiepileptic in dogs. Here we tested imepitoin for anxiolytic properties. In an model, imepitoin was capable of preventing the effect of corticotrophin releasing factor (CRF) on locus coeruleus neurons without suppressing the basal activity of these cells, an activity which is suggestive for an anti-stress effect of imepitoin. In addition, we applied a battery of standard rodent preclinical tests for anxiety behavior including elevated plus mazes in mice and rats, light-dark-box in mice and rats, social interaction test in rats, or the Vogel conflict test in rats. In all models, the observed profile of imepitoin appeared similar to benzodiazepines and typical for anxiolytic drugs. We also observed anxiolytic activity in dogs in a provoked open field sound-induced fear model, where reactions to noises were elicited by a sound recording of thunderstorms. Imepitoin caused an increase in locomotion measured in distance traveled and an ameliorating effect on cortisol levels in response to thunderstorm noises. For comparison, dexmedetomidine caused a decrease in locomotion and had no effect on cortisol. In all animal models the doses needed for an anxiolytic effect were not associated with sedation. In rodents, there was at least a factor of 10 between anxiolytic doses and doses with mild signs of sedation. In summary, imepitoin showed similar anxiolytic activities as benzodiazepines but without producing the known adverse reactions of benzodiazepines such as sedation.
艾美嘧啶是一种对γ-氨基丁酸(GABA)受体苯二氮䓬结合位点具有低亲和力的部分激动剂,目前在犬类中用作抗癫痫药物。在此,我们测试了艾美嘧啶的抗焦虑特性。在一个模型中,艾美嘧啶能够预防促肾上腺皮质激素释放因子(CRF)对蓝斑神经元的作用,而不抑制这些细胞的基础活性,这一活性提示艾美嘧啶具有抗应激作用。此外,我们应用了一系列标准的啮齿动物焦虑行为临床前测试,包括小鼠和大鼠的高架十字迷宫、小鼠和大鼠的明暗箱、大鼠的社交互动测试或大鼠的Vogel冲突测试。在所有模型中,观察到的艾美嘧啶的表现与苯二氮䓬类药物相似,是抗焦虑药物的典型表现。我们还在一个诱发的旷场声音诱发恐惧模型中观察到犬类的抗焦虑活性,在该模型中,通过雷暴的声音记录引发对噪音的反应。艾美嘧啶使以行进距离衡量的运动增加,并对雷暴噪音引起的皮质醇水平有改善作用。作为比较,右美托咪定使运动减少,且对皮质醇无影响。在所有动物模型中,产生抗焦虑作用所需的剂量与镇静作用无关。在啮齿动物中,抗焦虑剂量与有轻度镇静迹象的剂量之间至少相差10倍。总之,艾美嘧啶显示出与苯二氮䓬类药物相似的抗焦虑活性,但不会产生苯二氮䓬类药物已知的不良反应,如镇静作用。