Howard University College of Medicine, 520 W St., 20059 Washington, DC, United States.
Howard University College of Medicine, 520 W St., 20059 Washington, DC, United States.
Behav Brain Res. 2020 Jan 27;378:112156. doi: 10.1016/j.bbr.2019.112156. Epub 2019 Oct 5.
Women are at greater risk than men for developing posttraumatic stress disorder (PTSD) after trauma exposure. Sleep, especially rapid-eye-movement sleep (REMS), has been considered a contributing factor to the development of PTSD symptoms through its effects on the processing of emotional memories. However, it remains unknown if sex and sex hormones play a role in the hypothesized impact of sleep on the development of PTSD. Animal models have methodological advantages over human studies in investigating this research question; however, animal models of sleep in PTSD have been tested only with males. C57BL/6 mice (7 males and 15 females) were exposed to 15 footshocks in a footshock chamber, and 5 min after the last footshock, were returned to their home cages for telemetric electroencephalographic sleep recording. Nine to thirteen days later, mice were returned to the footshock chamber for 10 min without footshocks. Fear recall rates were computed by comparing freezing behaviors in the footshock chamber immediately after the footshocks to those during fear context reexposure. Males had significantly lower recall rates compared to metestrous females (that received footshocks on metestrus). Overall, males slept more than both proestrous females (that received footshocks on proestrus) and metestrous females during the dark period. Regression analyses revealed that average REMS episode durations after footshocks were differentially associated with recall rates across groups, such that the association was positive in males, but negative in proestrous females. Results suggest that both sex and the estrous cycle modulate the associations between REMS continuity and fear memory consolidation.
女性在创伤暴露后发展创伤后应激障碍(PTSD)的风险高于男性。睡眠,尤其是快速眼动睡眠(REMS),已被认为是通过对情绪记忆的处理影响 PTSD 症状发展的一个因素。然而,性别和性激素是否在睡眠对 PTSD 发展的假设影响中起作用仍不清楚。动物模型在研究这个研究问题方面具有比人类研究更大的方法学优势;然而,只有雄性动物进行了 PTSD 睡眠的动物模型测试。C57BL/6 小鼠(雄性 7 只,雌性 15 只)在足部电击室中接受 15 次足部电击,最后一次足部电击后 5 分钟,返回其家笼进行遥测脑电图睡眠记录。9 至 13 天后,将小鼠放回足部电击室 10 分钟而不进行足部电击。通过比较足部电击后立即在足部电击室中的冻结行为与恐惧情境重新暴露期间的冻结行为,计算出恐惧记忆的回忆率。与间情期雌性(在间情期接受足部电击)相比,雄性的回忆率明显降低。总体而言,雄性在黑暗期的睡眠时间多于动情前期雌性(在动情前期接受足部电击)和间情期雌性。回归分析显示,足部电击后平均 REMS 发作持续时间与各小组的回忆率存在差异关联,在雄性中呈正相关,而在动情前期雌性中呈负相关。结果表明,性别和发情周期都调节了 REMS 连续性与恐惧记忆巩固之间的关联。