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; Japanese Drug Organization of Appropriate Use and Research, Nagoya, Japan.
Division of Clinical Sciences and Neuropsychopharmacology, Faculty and Graduate School of Pharmacy, Meijo University, Nagoya, Japan.
Neuropharmacology. 2018 May 1;133:23-37. doi: 10.1016/j.neuropharm.2018.01.016. Epub 2018 Jan 11.
Adverse juvenile experiences, including physical abuse, often have negative health consequences later in life. We investigated the influence of social defeat stress exposure as juveniles on neuropsychological behaviors, and the causal role of glucocorticoids in abnormal behaviors and impairment of neurogenesis in mice exposed to the stress. The juvenile (24-day-old) and adult (70-day-old) male C57BL/6J mice were exposed to social defeat stress induced by an aggressive ICR mouse. Social defeat stress exposure as juveniles, even for 1 day, induced persistent social avoidance to the unfamiliar ICR mouse in the social interaction test, but that was not observed in mice exposed to the stress as adults. Social avoidance by the stress exposure as juveniles for 10 consecutive days was observed, when the target mouse was not only unfamiliar ICR but also another C57BL/J mouse, but not an absent or an anesthetized ICR mouse. The stress exposure did not induce anxiety- and depression-like behaviors in spontaneous locomotor activity, elevated plus-maze test, marble-burying test, forced swimming test, or sucrose preference test. Serum corticosterone levels increased immediately after the stress exposure. The hippocampal neurogenesis was suppressed 1 day and 4 weeks after the stress exposure. Administration of mifepristone, a glucocorticoid receptor antagonist, prior to each stress exposure, blocked the persistent social avoidance and suppression of neurogenesis. In conclusion, social avoidance induced by social defeat stress exposure as juveniles are more persistent than that as adults. These social avoidances are associated with suppression of hippocampal neurogenesis via glucocorticoid receptors.
不良的青少年经历,包括身体虐待,通常会对以后的生活造成负面影响。我们研究了青少年时期遭受社会挫败应激暴露对神经行为的影响,以及糖皮质激素在应激暴露小鼠异常行为和神经发生损伤中的因果作用。雄性 C57BL/6J 幼鼠(24 日龄)和成年鼠(70 日龄)暴露于攻击性 ICR 小鼠引起的社会挫败应激下。青少年时期(24 日龄)暴露于社会挫败应激,即使只有 1 天,也会导致在社交互动测试中对陌生的 ICR 小鼠持续回避,但成年期暴露于应激的小鼠则不会。在 10 天连续的应激暴露中,应激暴露的幼鼠会对目标小鼠(不仅是陌生的 ICR 小鼠,还有另一只 C57BL/J 小鼠)产生回避,但对不存在或麻醉的 ICR 小鼠则不会。应激暴露在自发运动活动、高架十字迷宫测试、大理石埋藏测试、强迫游泳测试或蔗糖偏好测试中均未引起焦虑和抑郁样行为。应激暴露后,血清皮质酮水平立即升高。应激暴露 1 天和 4 周后,海马神经发生受到抑制。在每次应激暴露前给予米非司酮(一种糖皮质激素受体拮抗剂),可阻断持续的社交回避和神经发生抑制。总之,与成年期相比,青少年时期遭受社会挫败应激暴露所引起的社交回避更为持久。这些社交回避与通过糖皮质激素受体抑制海马神经发生有关。