Hashimoto S, Inoue T, Koyama T
Department of Psychiatry, Hokkaidko University School of Medicine, Sapporo, Japan.
Psychopharmacology (Berl). 1996 Jan;123(2):182-6. doi: 10.1007/BF02246175.
Conditioned fear stress (CFS)-induced freezing behavior has been proposed as an animal model of anxiety. In the present study, freezing was used to determine the anxiolytic activity of selective serotonin reuptake inhibitors (SSRIs), which are reported to be clinically effective in anxiety disorders. The duration of freezing behavior was reduced by acute treatment with the SSRIs citalopram (1-10 mg/kg) and fluvoxamine (3-30 mg/kg). Acute treatment with the serotonin (5-HT)/noradrenaline (NA) mixed reuptake inhibitor milnacipran (3-30 mg/kg) also attenuated CFS-induced freezing, while acute treatment with the NA reuptake inhibitors maprotiline and ORG4428, and the dopamine (DA) reuptake inhibitor GBR12909 failed to alter CFS-induced freezing. These results indicate that facilitation of 5-HT availability in the brain produced by 5-HT reuptake inhibition reduces CFS-induced freezing behavior. CFS may be a useful model for detecting the anxiolytic potential of 5-HT reuptake inhibitors.
条件性恐惧应激(CFS)诱导的僵住行为已被提议作为一种焦虑症的动物模型。在本研究中,僵住行为被用于确定选择性5-羟色胺再摄取抑制剂(SSRI)的抗焦虑活性,据报道这些抑制剂在焦虑症的临床治疗中有效。用SSRI西酞普兰(1 - 10毫克/千克)和氟伏沙明(3 - 30毫克/千克)进行急性治疗可缩短僵住行为的持续时间。用5-羟色胺(5-HT)/去甲肾上腺素(NA)混合再摄取抑制剂米那普明(3 - 30毫克/千克)进行急性治疗也可减轻CFS诱导的僵住行为,而用NA再摄取抑制剂马普替林和ORG4428,以及多巴胺(DA)再摄取抑制剂GBR12909进行急性治疗则未能改变CFS诱导的僵住行为。这些结果表明,5-HT再摄取抑制所导致的大脑中5-HT可用性的增加可减少CFS诱导的僵住行为。CFS可能是一种用于检测5-HT再摄取抑制剂抗焦虑潜力的有用模型。