Bodnoff S R, Suranyi-Cadotte B, Quirion R, Meaney M J
Douglas Hospital Research Center, Department of Psychiatry, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
Psychopharmacology (Berl). 1989;97(2):277-9. doi: 10.1007/BF00442264.
We examined the anxiolytic effects of a variety of anti-depressant drugs, administered either acutely or chronically, in an animal model of anxiety involving novelty-suppressed feeding in food-deprived rats. Following a single injection of desipramine (10 mg/kg) amitriptyline (10 mg/kg), mianserin (10 mg/kg), fluoxetine (10 mg/kg), buspirone (4 mg/kg), gepirone (4 mg/kg) or nomifensine (10 mg/kg), there was no decrease in the latency to begin eating in the novel environment such as occurred with diazepam (2 mg/kg). In fact, an increased latency was observed for desipramine, amitriptyline, fluoxetine, and nomifensine. In contrast, chronic (21 days) treatment with each of the above-mentioned drugs, except nomifensine, significantly reduced the latency to begin eating relative to vehicle controls. These findings suggest that a variety of tricyclic and novel anti-depressant drugs acquire anxiolytic properties following chronic administration.
我们在一种涉及食物剥夺大鼠新奇抑制进食的焦虑动物模型中,研究了多种抗抑郁药物急性或慢性给药后的抗焦虑作用。单次注射地昔帕明(10毫克/千克)、阿米替林(10毫克/千克)、米安色林(10毫克/千克)、氟西汀(10毫克/千克)、丁螺环酮(4毫克/千克)、吉哌隆(4毫克/千克)或诺米芬辛(10毫克/千克)后,在新环境中开始进食的潜伏期并没有像注射地西泮(2毫克/千克)那样缩短。事实上,地昔帕明、阿米替林、氟西汀和诺米芬辛的潜伏期反而延长了。相比之下,除诺米芬辛外,上述每种药物进行慢性(21天)治疗后,相对于溶剂对照组,开始进食的潜伏期显著缩短。这些发现表明,多种三环类和新型抗抑郁药物在慢性给药后会获得抗焦虑特性。