DePoy Lauren M, Vadnie Chelsea A, Petersen Kaitlyn A, Scott Madeline R, Zong Wei, Yin RuoFei, Matthaei Ross C, Anaya Fernanda Juarez, Kampe Callie I, Tseng George C, McClung Colleen A
Department of Psychiatry, Translational Neuroscience Program, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, United States.
Front Neurosci. 2024 Dec 16;18:1478508. doi: 10.3389/fnins.2024.1478508. eCollection 2024.
Circadian rhythm disturbances have long been associated with the development of psychiatric disorders, including mood and substance use disorders. Adolescence is a particularly vulnerable time for the onset of psychiatric disorders and for circadian rhythm and sleep disruptions. Preclinical studies have found that circadian rhythm disruption (CRD) impacts the brain and behavior, but this research is largely focused on adult disruptions. Here, we hypothesized that adolescent CRD would have a greater effect on psychiatric-related behaviors, relative to adult disruption.
We determined the long-term behavioral and neurobiological effects of CRD during early adolescence by exposing mice to 12 h shifts in the light/dark cycle. Adult mice were exposed to the same CRD paradigm. Behavior testing began approximately 4 weeks later for both groups. To identify possible mechanisms, we also measured gene expression in brain regions relevant to circadian rhythms, mood and reward.
CRD during early adolescence, but not adulthood, persistently increased exploratory drive (risk-taking behavior) and cocaine preference when tested later in life. Interestingly, we found sex differences when intravenous cocaine self-administration was tested. While female mice with a history of adolescent CRD had a greater propensity to self-administer cocaine, as well as increased motivation and cue-induced reinstatement, male adolescent CRD mice had reduced motivation and extinction responding. Importantly, we found that transcripts in the SCN were affected by adolescent CRD and these were largely distinct across sex.
Overall, adolescent CRD in mice caused persistent increases in risky behavior, cocaine reward and cocaine self-administration, which suggests that CRD during adolescence may predispose individuals toward substance use disorders. Future research is required to elucidate how adolescent CRD affects behaviors relevant to mood-and substance use-related disorders across the 24-h day, as well as to identify intervention strategies to alleviate disruption during adolescence and novel therapeutic approaches once symptoms have begun.
昼夜节律紊乱长期以来一直与精神疾病的发生有关,包括情绪和物质使用障碍。青春期是精神疾病发病以及昼夜节律和睡眠中断的特别脆弱时期。临床前研究发现昼夜节律紊乱(CRD)会影响大脑和行为,但这项研究主要集中在成人的昼夜节律紊乱上。在这里,我们假设相对于成人的昼夜节律紊乱,青少年的昼夜节律紊乱对与精神疾病相关的行为有更大的影响。
我们通过将小鼠暴露于12小时的光/暗周期变化中,来确定青春期早期昼夜节律紊乱的长期行为和神经生物学影响。成年小鼠也暴露于相同的昼夜节律紊乱模式。两组小鼠大约在4周后开始进行行为测试。为了确定可能的机制,我们还测量了与昼夜节律、情绪和奖赏相关的脑区中的基因表达。
青春期早期而非成年期的昼夜节律紊乱,在后期测试时会持续增加探索驱动力(冒险行为)和对可卡因的偏好。有趣的是,在测试静脉注射可卡因自我给药时,我们发现了性别差异。虽然有青春期昼夜节律紊乱史的雌性小鼠有更强的自我给药可卡因的倾向,以及更高的动机和线索诱导的复吸,但青春期昼夜节律紊乱的雄性小鼠动机降低且消退反应减弱。重要的是,我们发现视交叉上核中的转录本受青春期昼夜节律紊乱影响,并且在不同性别中差异很大。
总体而言,小鼠青春期的昼夜节律紊乱导致冒险行为、可卡因奖赏和可卡因自我给药持续增加,这表明青春期的昼夜节律紊乱可能使个体易患物质使用障碍。未来需要开展研究,以阐明青春期的昼夜节律紊乱如何在全天24小时内影响与情绪和物质使用相关障碍有关的行为,以及确定缓解青春期昼夜节律紊乱的干预策略和症状出现后的新治疗方法。