Louis Caroline, Cohen Caroline, Depoortère Ronan, Griebel Guy
CNS Research Department, Sanofi-Aventis, Bagneux, France.
Neuropsychopharmacology. 2006 Oct;31(10):2180-7. doi: 10.1038/sj.npp.1301036. Epub 2006 Feb 1.
The vasopressin 1b receptor antagonist, SSR149415, and the corticotropin-releasing factor 1 receptor antagonist, SSR125543, are orally active non-peptidic compounds with anxiolytic- and antidepressant-like activities in animal models. Presently, SSR149415 and SSR125543 were evaluated in a differential reinforcement of low-rate 72 s (DRL-72 s) schedule, a procedure known to respond differentially to antidepressants and anxiolytics. Male Wistar rats were trained to lever-press for food reinforcement, but only lever-presses occurring after a 72 s delay were reinforced; otherwise, presses were not rewarded, and the timer was reset to 0 s. The selective serotonin reuptake inhibitor, fluoxetine, and the benzodiazepine anxiolytic, diazepam, were tested in parallel. SSR149415 (10-30 mg/kg, i.p.) and SSR125543 (30 mg/kg, i.p.) increased the percentage of responses emitted in the inter-response time (IRT) bin (49-96 s), which resulted in a greater number of reinforced presses. Both compounds shifted the frequency distribution of responses toward longer IRT durations, with a preservation of the bell shape of the IRT distribution curve. Fluoxetine (10 mg/kg, i.p.) had an effect on DRL-72 s similar to that of SSR149415 and SSR125543. By contrast, diazepam increased the number of responses in IRT bin (0-12 s), and the IRT distribution curve was shifted toward shorter IRT durations and flattened. In summary, these results show that SSR149415 and SSR125543 displayed antidepressant-like activity in a DRL-72 s schedule in rat, confirming their therapeutic potential for the treatment of pathological states induced by chronic frustration such as depression.
血管加压素1b受体拮抗剂SSR149415和促肾上腺皮质激素释放因子1受体拮抗剂SSR125543是具有口服活性的非肽类化合物,在动物模型中具有抗焦虑和抗抑郁样活性。目前,在低速率72秒差异强化(DRL - 72 s)程序中对SSR149415和SSR125543进行了评估,该程序对抗抑郁药和抗焦虑药有不同反应。雄性Wistar大鼠经训练通过杠杆按压获取食物强化,但只有在延迟72秒后发生的杠杆按压才会得到强化;否则,按压不会得到奖励,定时器重置为0秒。同时对选择性5-羟色胺再摄取抑制剂氟西汀和苯二氮䓬类抗焦虑药地西泮进行了测试。SSR149415(10 - 30毫克/千克,腹腔注射)和SSR125543(30毫克/千克,腹腔注射)增加了反应间隔时间(IRT)区间(49 - 96秒)内发出反应的百分比,从而导致更多的强化按压。两种化合物都将反应的频率分布向更长的IRT持续时间转移,同时保留了IRT分布曲线的钟形。氟西汀(10毫克/千克,腹腔注射)对DRL - 72 s的作用与SSR149415和SSR125543相似。相比之下,地西泮增加了IRT区间(0 - 12秒)内的反应数量,IRT分布曲线向更短的IRT持续时间转移并变平。总之,这些结果表明,SSR149415和SSR125543在大鼠DRL - 72 s程序中表现出抗抑郁样活性,证实了它们在治疗由慢性挫折诱导的病理状态(如抑郁症)方面的治疗潜力。