Department of Pharmacology, Biological Sciences Sector, Federal University of Paraná, Centro Politécnico, C.P. 19031, 81540-990 Curitiba, PR, Brazil.
Institute of Biophysics Carlos Chagas Filho & Institute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro, RJ 21941-590, Brazil.
Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jan 10;88:142-150. doi: 10.1016/j.pnpbp.2018.07.002. Epub 2018 Jul 5.
Mania is characterized by elevated drive and mood but animal models of mania have often neglected elevated mood. Ultrasonic vocalizations (USV) of 50-kHz emitted by rats are thought to index the subject's positive affective state. Fifty-kHz USV emission is increased by amphetamine, an effect blocked by lithium administration. Sleep deprivation (SD) is an environmental model of mania and the present study evaluated SD effects on behavioral activity and USV emission, together with the impact of lithium treatment. Adult rats were submitted to 24h or 72h SD, and locomotor activity and USV emission were assessed. To test their sensitivity to a standard antimanic drug, these behavioral parameters were also evaluated after acute administration of lithium carbonate (25, 50 or 100 mg/kg, i.p.). Striatal monoamine content was measured post-mortem. SD (24h and 72h) led to increased locomotor activity, rearing behavior and 50-kHz USV emission, together with a change in the call profile characterized by an increase in the percentage of frequency-modulated 50-kHz USV, which may indicate the mania-like consequences of SD. Importantly, all SD effects were reverted by lithium administration. SD also led to a decrease in dopamine content in the ventral striatum, while increasing dopamine turnover. In conclusion, SD increased 50-kHz USV emission, an effect prevented by acute lithium administration. This suggests 50-kHz USV as a new marker for mania-like elevated mood, which shows construct validity (associated with increased dopaminergic tone), face validity (reflecting increased positive affect) and predictive validity (high sensitivity to lithium treatment).
躁狂症的特征是情绪高涨和驱动力增强,但躁狂症的动物模型往往忽略了情绪的升高。大鼠发出的 50kHz 超声发声(USV)被认为可以反映动物的积极情绪状态。安非他命会增加 50kHz USV 的发射,而锂的给药会阻断这一效应。睡眠剥夺(SD)是躁狂症的一种环境模型,本研究评估了 SD 对行为活动和 USV 发射的影响,以及锂治疗的影响。成年大鼠接受 24 小时或 72 小时的 SD,评估其运动活动和 USV 发射。为了测试它们对标准抗躁狂药物的敏感性,还评估了锂碳酸酯(25、50 或 100mg/kg,ip)急性给药后这些行为参数。死后测量纹状体中单胺类物质的含量。SD(24 小时和 72 小时)导致运动活动、竖起行为和 50kHz USV 发射增加,以及叫声特征的改变,表现为调频 50kHz USV 的百分比增加,这可能表明 SD 的类似躁狂症的后果。重要的是,锂给药逆转了所有的 SD 效应。SD 还导致腹侧纹状体中的多巴胺含量降低,同时增加多巴胺的周转率。总之,SD 增加了 50kHz USV 发射,急性锂给药可预防这种效应。这表明 50kHz USV 是一种新的躁狂症样情绪升高的标志物,具有结构有效性(与增加的多巴胺能张力相关)、表面有效性(反映增加的积极情绪)和预测有效性(对锂治疗高度敏感)。