Department of Pharmacology, Universidade Federal de São Paulo, R. Botucatu, 862, Ed. Leal Prado, 1° andar, 04023062 São Paulo, SP, Brazil; Department of Psychobiology, Universidade Federal de São Paulo, R. Napoleão de Barros, 925, 3° andar, 04024002 São Paulo, SP, Brazil.
Department of Pharmacology, Universidade Federal de São Paulo, R. Botucatu, 862, Ed. Leal Prado, 1° andar, 04023062 São Paulo, SP, Brazil.
Psychiatry Res. 2014 Aug 30;218(3):335-40. doi: 10.1016/j.psychres.2014.04.046. Epub 2014 May 9.
Drug-induced behavioral sensitization (BS), paradoxical sleep deprivation (PSD) and adolescence in rodents are associated with changes in the mesolimbic dopaminergic system. We compared the effects of PSD on amphetamine-induced BS in adult and adolescent mice. Adult (90 days old) and adolescent (45 days old) Swiss mice were subjected to PSD for 48h. Immediately after PSD, mice received saline or 2.0mg/kg amphetamine intraperitoneally (i.p.), and their locomotion was quantified in activity chambers. Seven days later, all the animals were challenged with 2.0mg/kg amphetamine i.p., and their locomotion was quantified again. Acute amphetamine enhanced locomotion in both adult and adolescent mice, but BS was observed only in adolescent mice. Immediately after its termination, PSD decreased locomotion of both saline- and amphetamine-treated adolescent mice. Seven days later, previous PSD potentiated both the acute stimulatory effect of amphetamine and its sensitization in adolescent mice. In adult animals, previous PSD revealed BS. Our data suggest that adolescent mice are more vulnerable to both the immediate and long-term effects of PSD on amphetamine-induced locomotion. Because drug-induced BS in rodents shares neuroplastic changes with drug craving in humans, our findings also suggest that both adolescence and PSD could facilitate craving-related mechanisms in amphetamine abuse.
药物诱导的行为敏化(BS)、反常性睡眠剥夺(PSD)和啮齿动物的青春期与中脑边缘多巴胺能系统的变化有关。我们比较了 PSD 对成年和青春期小鼠安非他命诱导的 BS 的影响。成年(90 天大)和青春期(45 天大)瑞士小鼠接受 PSD48 小时。PSD 后立即,小鼠接受生理盐水或 2.0mg/kg 安非他命腹膜内(i.p.)注射,并在活动室中定量其运动。7 天后,所有动物均接受 2.0mg/kg 安非他命 i.p. 挑战,再次定量其运动。急性安非他命增强了成年和青春期小鼠的运动,但仅在青春期小鼠中观察到 BS。PSD 终止后,立即降低了生理盐水和安非他命处理的青春期小鼠的运动。7 天后,先前的 PSD 增强了安非他命的急性刺激作用及其在青春期小鼠中的敏化作用。在成年动物中,先前的 PSD 显示出 BS。我们的数据表明,青春期小鼠更容易受到 PSD 对安非他命诱导的运动的即时和长期影响。由于啮齿动物的药物诱导 BS 与人类的药物渴望的神经可塑性变化有关,我们的研究结果还表明,青春期和 PSD 都可能促进安非他命滥用中与渴望相关的机制。