Division of Clinical Sciences and Neuropsychopharmacology, Faculty and Graduate School of Pharmacy, Meijo University, Nagoya, Japan.
Advanced Diagnostic System Research Laboratory, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.
Int J Neuropsychopharmacol. 2018 Sep 1;21(9):837-846. doi: 10.1093/ijnp/pyy038.
Extensive studies have been performed on the role of monoaminergic neuronal systems in rodents exposed to social defeat stress as adults. In the present study, we investigated the role of monoaminergic neuronal systems in the impairment of social behaviors induced by social defeat stress exposure as juveniles.
Juvenile, male C57BL/6J mice were exposed to social defeat stress for 10 consecutive days. From 1 day after the last stress exposure, desipramine, sertraline, and aripiprazole were administered for 15 days. Social behaviors were assessed at 1 and 15 days after the last stress exposure. Monoamine turnover was determined in specific regions of the brain in the mice exposed to the stress.
Stress exposure as juveniles induced the impairment of social behaviors in adolescent mice. In mice that showed impairment of social behaviors, turnover of serotonin and dopamine, but not noradrenaline, was decreased in specific brain regions. Acute and repeated administration of desipramine, sertraline, and aripiprazole failed to attenuate the impairment of social behaviors, whereas repeated administration of a combination of sertraline and aripiprazole showed additive attenuating effects.
These findings suggest that social defeat stress exposure as juveniles induces the treatment-resistant impairment of social behaviors in adolescents through dysfunction in the serotonergic and dopaminergic neuronal systems. The combination of sertraline and aripiprazole may be used as a new treatment strategy for treatment-resistant stress-related psychiatric disorders in adolescents with adverse juvenile experiences.
大量研究已经证实,单胺能神经元系统在成年期遭受社交挫败应激的啮齿类动物中发挥着重要作用。在本研究中,我们探讨了单胺能神经元系统在幼年时期遭受社交挫败应激后引起的社交行为障碍中的作用。
雄性 C57BL/6J 幼鼠连续 10 天接受社交挫败应激。从最后一次应激暴露后的第 1 天开始,给予去甲丙咪嗪、舍曲林和阿立哌唑治疗 15 天。在最后一次应激暴露后的第 1 天和第 15 天评估社交行为。检测应激暴露小鼠大脑特定区域中单胺类物质的周转率。
幼年时期的应激暴露导致青少年小鼠的社交行为受损。在表现出社交行为受损的小鼠中,特定脑区的 5-羟色胺和多巴胺周转率降低,但去甲肾上腺素周转率没有降低。急性和重复给予去甲丙咪嗪、舍曲林和阿立哌唑均不能减轻社交行为的损伤,而重复给予舍曲林和阿立哌唑的组合则显示出相加的减轻作用。
这些发现表明,幼年时期的社交挫败应激暴露通过 5-羟色胺能和多巴胺能神经元系统的功能障碍,导致青少年时期出现治疗抵抗性的社交行为损伤。舍曲林和阿立哌唑的联合应用可能为具有不良青少年经历的青少年应激相关精神障碍的治疗抵抗提供一种新的治疗策略。