Ledesma-Corvi Sandra, Hernández-Hernández Elena, García-Fuster M Julia
IUNICS, University of the Balearic Islands, Palma, Spain.
Health Research Institute of the Balearic Islands (IdISBa), Palma, Spain.
Transl Psychiatry. 2022 Jun 1;12(1):220. doi: 10.1038/s41398-022-01994-y.
There is an urgent need for developing novel pharmacological treatment options for adolescent depression, and to ensure an optimal translational outcome to the clinic, sex should be included as a biological variable in preclinical studies. In this context, the present study compared the antidepressant-like potential of ketamine and cannabidiol, with the clinical standard fluoxetine, in adolescent rats exposed to maternal deprivation (as a model of early-life stress), while including a sex perspective. Moreover, changes in drug efficacy over time were evaluated by re-exposing rats to the same dose regimens during adulthood. Antidepressant-like responses were scored through a battery of distinctive tests (forced-swim, novelty-suppressed feeding, and sucrose preference) across time. The main results proved an antidepressant-like potential for ketamine and cannabidiol in adolescent rats, although their efficacy was dependent on sex and prior stress exposure, as well as on treatment length and the behavioral feature analyzed. In general, while all tested antidepressants in male rats improved certain affective-like features, female rats were mainly unresponsive to the treatments performed (except for certain benefits induced by ketamine), demonstrating the need for further characterizing proper treatments for this particular sex. Moreover, when rats were re-exposed in adulthood to the same drug regimens as in adolescence, a drop in efficacy was observed. These findings may have translational ramifications in that ketamine or cannabidiol could be moved forward as antidepressants for the adolescent depressed population, but not before further characterizing their potential long-term safety and/or beneficial vs. harmful effects for both sexes.
迫切需要开发针对青少年抑郁症的新型药物治疗方案,为确保最佳的临床转化结果,在临床前研究中应将性别作为生物学变量纳入考量。在此背景下,本研究比较了氯胺酮和大麻二酚与临床标准药物氟西汀在经历母婴分离(作为早期生活应激模型)的青春期大鼠中的抗抑郁样潜力,同时纳入了性别视角。此外,通过在成年期让大鼠再次接受相同剂量方案来评估药物疗效随时间的变化。通过一系列独特的测试(强迫游泳、新奇抑制摄食和蔗糖偏好)在不同时间对抗抑郁样反应进行评分。主要结果证明氯胺酮和大麻二酚在青春期大鼠中具有抗抑郁样潜力,尽管它们的疗效取决于性别、先前的应激暴露、治疗时长以及所分析的行为特征。总体而言,虽然所有测试的抗抑郁药在雄性大鼠中改善了某些类似情感的特征,但雌性大鼠对所进行的治疗主要无反应(氯胺酮诱导的某些益处除外),这表明需要进一步确定针对这一特定性别的合适治疗方法。此外,当成年大鼠再次接受与青春期相同的药物方案时,观察到疗效下降。这些发现可能具有转化意义,即氯胺酮或大麻二酚可作为青少年抑郁症患者的抗抑郁药进一步研究,但在此之前需要进一步确定它们对两性潜在的长期安全性和/或有益与有害影响。