Atrooz Fatin, Alrousan Ghalya, Hassan Arham, Salim Samina
Department of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, United States.
Front Neurosci. 2022 Apr 25;16:856120. doi: 10.3389/fnins.2022.856120. eCollection 2022.
Evidence in the literature suggests that sleep deprivation during early-life developmental stages, by impacting important processes such as the reward circuit maturation, may increase the vulnerability for alcohol and substance use. The mechanisms involved are not fully understood. In this study, utilizing our previously established model, we examined the impact of early-life sleep deprivation on alcohol consumption in adolescent rats. Male Sprague Dawley rats served as either the control (CON) or sleep-deprived (SD) group. Sleep deprivation was induced using a Pinnacle automated sleep deprivation apparatus. The SD group of rats was sleep deprived for 6-8 h/day for 14 days from postnatal day (PND)19 to PND32. At PND33, anxiety- and depression-like behaviors were assessed in rats using elevated plus maze and sucrose splash test, respectively. At PND39, alcohol consumption was assessed in rats for five consecutive days using the two-bottle choice paradigm, water versus 5% ethanol. SD rats exhibited significant anxiety- and depression-like behaviors as compared to CON rats. Interestingly, SD rats consumed a larger volume of alcohol when compared to CON rats, which was significantly higher at day 5 (mean of alcohol consumption (ml) ± SD; CON = 6.67 ± 3.42; SD = 19.00 ± 6.05, = 0.0126). SD rats also showed high preference for alcohol over water, which was significantly higher at day 5 (mean of alcohol preference (%) ± SD; CON = 26.85 ± 14.97; SD = 57.69 ± 5.61, = 0.014). Our data suggest that early-life sleep deprivation enhanced alcohol consumption in adolescent rats.
文献中的证据表明,在生命早期发育阶段睡眠不足,可能会通过影响诸如奖赏回路成熟等重要过程,增加酒精和药物使用的易感性。其中涉及的机制尚未完全了解。在本研究中,我们利用先前建立的模型,研究了生命早期睡眠不足对青春期大鼠酒精摄入量的影响。雄性斯普拉格·道利大鼠作为对照组(CON)或睡眠剥夺组(SD)。使用Pinnacle自动睡眠剥夺装置诱导睡眠剥夺。SD组大鼠从出生后第19天(PND19)至PND32每天睡眠剥夺6 - 8小时,持续14天。在PND33时,分别使用高架十字迷宫和蔗糖溅落试验评估大鼠的焦虑样和抑郁样行为。在PND39时,使用双瓶选择范式(水与5%乙醇)连续五天评估大鼠的酒精摄入量。与CON组大鼠相比,SD组大鼠表现出显著的焦虑样和抑郁样行为。有趣的是,与CON组大鼠相比,SD组大鼠摄入的酒精量更大,在第5天显著更高(酒精摄入量平均值(ml)±标准差;CON = 6.67 ± 3.42;SD = 19.00 ± 6.05,P = 0.0126)。SD组大鼠对酒精的偏好也高于水,在第5天显著更高(酒精偏好平均值(%)±标准差;CON = 26.85 ± 14.97;SD = 57.69 ± 5.61,P = 0.014)。我们的数据表明,生命早期睡眠剥夺会增加青春期大鼠的酒精摄入量。