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Enhancement of immobility in a forced swimming test by subacute or repeated treatment with phencyclidine: a new model of schizophrenia

机译:亚急性或苯环利定反复治疗可增强强制游泳试验的不动能力:一种新型的精神分裂症模型

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1 Immobility induced by forced swimming is well known as an animal model of depression. To develop an animal model for the negative symptoms of schizophrenia, in particular the depressive symptoms, the effect of phencyclidine (PCP) on immobility in the forced swimming test was investigated in mice, since PCP produces such negative symptoms in humans. 2 Repeated treatment with PCP (10 mg kg~(-1) day~(-1), s.c, once a day for 14 days) prolonged the immobility time in the forced swimming test 24 h after the final injection compared with saline treatment; the effect was not obtained by single or 5 treatments with PCP (10 mg kg~(-1), s.c), or by repeated treatment with methamphetamine (0.5 and 1 mg kg~(-1) day~(-1), s.c, once a day for 14 days). 3 The enhancing effect of PCP (10 mg kg~(-1) day~(-1), s.c.) on the immobility persisted for at least 21 days after the withdrawal of the drug. 4 Haloperidol (0.3 and 1 mg kg~(-1), p.o.), ritanserin (3 and 10 mg kg~(-1), p.o.), risperidone (0.1-1 mg kg~(-1), p.o.), and clozapine (3 and 10 mg kg~(-1), p.o.) failed to attenuate the immobility induced by the forced swimming in mice repeatedly treated with saline when the drugs were administered 1 h before the forced swimming test. However, ritanserin (30 mg kg~(-1)) and clozapine (30 mg kg~(-1)) did attenuate this immobility. 5 The enhancing effect of PCP on the immobility was attenuated by ritanserin (3 and 10 mg kg~(-1), p.o.), risperidone (0.3 mg kg~(-1), p.o.), and clozapine (3 and 10 mg kg~(-1), p.o.), whereas haloperidol (0.3 and 1 mg kg~(-1), p.o.) had no effect. 6 These results suggest that the enhancement of immobility in the forced swimming test brought about by repeated PCP treatment could be used as a model of the negative symptoms, particularly the depression, of schizophrenia. This effect of PCP appeared to be mediated, at least in part, via 5-HT_(2A) receptors.
机译:1由强迫游泳引起的不动是众所周知的抑郁症动物模型。为了建立用于精神分裂症的阴性症状,特别是抑郁症状的动物模型,在小鼠中研究了苯环利定(PCP)对不动的不动性的影响,因为PCP在人中产生了这种阴性症状。 2重复注射PCP(10 mg kg〜(-1)天〜(-1)天,皮下注射,每天一次,连续14天)延长了最终注射后24 h强迫游泳试验中的固定时间,与盐水治疗相比;单次或连续5次用PCP(10 mg kg〜(-1),sc)或通过重复使用甲基苯丙胺(0.5和1 mg kg〜(-1)day〜(-1),sc)不能获得效果,每天一次,共14天)。 3 PCP(10 mg kg〜(-1)day〜(-1),s.c.)的增强作用在停药后至少持续21天。 4氟哌啶醇(0.3和1 mg kg〜(-1),po),利坦色林(3和10 mg kg〜(-1),po),利培酮(0.1-1 mg kg〜(-1),po)和氯氮平(3和10 mg kg〜(-1),口服)在强制游泳试验前1 h反复用盐水治疗的小鼠中,不能减弱强迫游泳引起的固定性。然而,利坦色林(30 mg kg〜(-1))和氯氮平(30 mg kg〜(-1))确实减弱了这种固定性。 5利坦色林(3和10 mg kg〜(-1),po),利培酮(0.3 mg kg〜(-1),po)和氯氮平(3和10 mg kg)减弱了PCP对固定性的增强作用。 〜(-1),po),而氟哌啶醇(0.3和1 mg kg〜(-1),po)没有作用。 6这些结果表明,通过反复进行PCP治疗可增强强迫游泳试验中的不动能力,可作为精神分裂症阴性症状(尤其是抑郁症)的模型。 PCP的这种作用似乎至少部分是通过5-HT_(2A)受体介导的。

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