Fratta W, Collu M, Martellotta M C, Pichiri M, Muntoni F, Gessa G L
Department of Neuroscience, University of Cagliari, Italy.
Eur J Pharmacol. 1987 Oct 27;142(3):437-40. doi: 10.1016/0014-2999(87)90084-7.
REM sleep deprivation induced by means of the platform technique (72 h) was followed by a period of latency to sleep characterized by a marked excitement in rats. The administration of naloxone at the end of the REM deprivation period reduced this latency to sleep while morphine, beta-endorphin and DADLE prolonged it. The dopamine D1 receptor antagonist SCH 23390 was extremely potent (0.003 mg/kg) to reduce the latency to sleep and the excitement while the D1 agonist SKF 38393 induced an opposite effect. The dopamine D2 receptor antagonist L-sulpiride was inactive up to a dose of 25 mg/kg. These data suggest that hyperactivity of the opioid and dopamine systems (specifically mediated through D1 receptors) is involved in such behaviour.
采用平台技术诱导大鼠快速眼动睡眠剥夺72小时后,出现一段睡眠潜伏期,其特征为大鼠明显兴奋。在快速眼动睡眠剥夺期结束时给予纳洛酮可缩短这种睡眠潜伏期,而吗啡、β-内啡肽和DADLE则延长该潜伏期。多巴胺D1受体拮抗剂SCH 23390(0.003 mg/kg)能极其有效地缩短睡眠潜伏期并减轻兴奋程度,而D1激动剂SKF 38393则产生相反的效果。多巴胺D2受体拮抗剂L-舒必利在高达25 mg/kg的剂量下无活性。这些数据表明,阿片类和多巴胺系统的多动(特别是通过D1受体介导)与这种行为有关。