Vogel G, Neill D, Hagler M, Kors D
Department of Psychiatry, Emory University School of Medicine, Atlanta, GA 30306.
Neurosci Biobehav Rev. 1990 Spring;14(1):85-91. doi: 10.1016/s0149-7634(05)80164-2.
In 1982 our laboratory proposed a new animal model of endogenous depression. The proposal was that in rats, neonatally administered clomipramine (CLI) will produce adult animals that model endogenous depression. We summarize here several tests of the validity of the model. Results were that after neonatal CLI, adult male rats showed behavioral abnormalities of the human disorder: decreased sexual, aggressive, and intracranial self-stimulation activities, as well as motor hyperactivity in a stressful situation. Preliminary evidence suggested that behavioral abnormalities in rats (sexual, aggressive, and motor) briefly treated with antidepressant treatments (imipramine, REM sleep deprivation) begin to normalize. Lastly, after neonatal CLI, the adult rats showed REM sleep abnormalities of endogenous depression, viz, low REM latency, frequent sleep onset REM periods, and abnormal temporal course of REM rebound after REM sleep deprivation. These results supported the hypothesis that in rats neonatal CLI produced adult animals that modelled endogenous depression.
1982年,我们实验室提出了一种新的内源性抑郁症动物模型。该模型是基于给新生大鼠注射氯米帕明(CLI),从而培育出可模拟内源性抑郁症的成年动物。在此,我们总结了该模型有效性的多项测试。结果显示,新生期接受CLI处理后,成年雄性大鼠出现了人类该疾病的行为异常:性行为、攻击行为及颅内自我刺激活动减少,以及在应激状态下出现运动活动亢进。初步证据表明,经抗抑郁治疗(丙咪嗪、快速眼动睡眠剥夺)短暂处理的大鼠(性行为、攻击行为及运动行为方面)的行为异常开始恢复正常。最后,新生期接受CLI处理后,成年大鼠出现了内源性抑郁症的快速眼动睡眠异常,即快速眼动睡眠潜伏期缩短、睡眠开始时频繁出现快速眼动期,以及快速眼动睡眠剥夺后快速眼动反弹的异常时间进程。这些结果支持了以下假说:新生期接受CLI处理的大鼠培育出的成年动物可模拟内源性抑郁症。