Garcia-Carachure Israel, Flores-Ramirez Francisco J, Castillo Samuel A, Themann Anapaula, Arenivar Miguel A, Preciado-Piña Joshua, Zavala Arturo R, Lobo Mary Kay, Iñiguez Sergio D
Department of Psychology, The University of Texas at El Paso, El Paso, TX, USA.
Department of Psychology, California State University, Long Beach, CA, USA.
Neuropsychopharmacology. 2020 Aug;45(9):1536-1544. doi: 10.1038/s41386-020-0654-7. Epub 2020 Mar 12.
Ketamine has shown promising antidepressant efficacy for adolescent treatment-resistant depression. However, the potential enduring consequences of ketamine exposure have not been thoroughly evaluated. Thus, we examined if juvenile ketamine treatment results in long-lasting changes for the rewarding properties of sucrose and cocaine in adulthood, across three separate experiments. In Experiment 1, adolescent male and female C57BL/6 mice received ketamine (20 mg/kg) for 15 consecutive days (Postnatal Day [PD] 35-49). Twenty-one days later (PD70; adulthood) we examined their behavioral responsivity to sucrose (1%) on a two-bottle choice design, or cocaine (0, 5, 10 mg/kg) using the conditioned place preference (CPP) test. We found that juvenile ketamine-pretreatment increased preference for sucrose and environments paired with cocaine in male, but not female, adult mice. This long-term outcome was not observed when male and female mice received ketamine as adults (PD70-84) and tested for sucrose and cocaine preference 21-days later (Experiment 2). Similarly, in Experiment 3, no long-lasting differences in these measures were observed when adolescent male mice were exposed to concomitant ketamine and social stressors (PD35-44), namely the social defeat or vicarious defeat stress paradigms-procedures that mediated a depression-related phenotype (along with a ketamine antidepressant-like response). Collectively, we demonstrate that in the absence of physical or psychological stress, adolescent ketamine exposure increases later life preference for the rewarding properties of sucrose and cocaine in a sex- and age-specific manner. As such, this preclinical work provides awareness for the potential long-term behavioral consequences associated with juvenile ketamine exposure.
氯胺酮已显示出对青少年难治性抑郁症有可观的抗抑郁疗效。然而,氯胺酮暴露的潜在长期后果尚未得到充分评估。因此,我们通过三个独立实验,研究了幼年氯胺酮治疗是否会导致成年期蔗糖和可卡因奖赏特性的持久变化。在实验1中,青春期雄性和雌性C57BL/6小鼠连续15天接受氯胺酮(20毫克/千克)(出生后第[PD]35 - 49天)。21天后(PD70;成年期),我们在双瓶选择设计中检测它们对蔗糖(1%)的行为反应,或使用条件性位置偏爱(CPP)试验检测对可卡因(0、5、10毫克/千克)的行为反应。我们发现,幼年氯胺酮预处理增加了成年雄性小鼠对蔗糖以及与可卡因配对环境的偏爱,但成年雌性小鼠没有。当雄性和雌性小鼠成年后(PD70 - 84)接受氯胺酮治疗,并在21天后检测蔗糖和可卡因偏爱时,未观察到这种长期结果(实验2)。同样,在实验3中,当青春期雄性小鼠同时暴露于氯胺酮和社会应激源(PD35 - 44)时,即在社会挫败或替代性挫败应激范式(介导与抑郁相关表型的程序,以及氯胺酮类抗抑郁反应)下,这些指标也未观察到持久差异。总体而言,我们证明,在没有身体或心理应激的情况下,青春期氯胺酮暴露会以性别和年龄特异性方式增加成年后对蔗糖和可卡因奖赏特性的偏爱。因此,这项临床前研究为幼年氯胺酮暴露相关的潜在长期行为后果提供了认识。