Division of Medical Pharmacology, Leiden Academic Center for Drug Research, Leiden University Medical Center, Leiden University, Leiden, The Netherlands; Department of Endocrinology and Metabolism, Leiden University Medical Center, Leiden University, Leiden, The Netherlands; Traumatic Stress Studies Division & Laboratory of Molecular Neuropsychiatry, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, USA; Mental Health Care Center, PTSD Clinical Research Program and Laboratory of Clinical Neuroendocrinology and Neurochemistry, James J. Peters Veterans Affairs Medical Center, Bronx, USA.
Division of Medical Pharmacology, Leiden Academic Center for Drug Research, Leiden University Medical Center, Leiden University, Leiden, The Netherlands; Laboratory of Biology-Biochemistry, Faculty of Nursing, School of Health Sciences, University of Athens, Greece; Department of Psychiatry, Columbia University, New York, NY, USA.
Psychoneuroendocrinology. 2014 Jan;39:39-57. doi: 10.1016/j.psyneuen.2013.09.021. Epub 2013 Sep 27.
Prolonged maternal separation (MS) activates the neonate's hypothalamus-pituitary-adrenal axis causing elevated basal and stress-induced corticosterone levels that may initiate amygdala-dependent fear learning. Here we test the hypothesis that the adult fearful phenotype is programmed by the pup's stressful experience during prolonged MS rather than by prolonged maternal absence per se. For this purpose, Wistar rat pups were exposed, on postnatal-day (pnd) 3, to: (i) repeated-MS in home-environment (HOME-SEP), 8h-MS daily for three days with the pups remaining together in the home-cage; (ii) repeated-MS in a novel-environment (NOVEL-SEP), with the same separation procedure, but now the pups were individually housed in a novel-environment during the 8h dam's absence; (iii) repeated handling, which consisted of daily brief (15 min instead of 8h) MS in the home-altogether or in a novel-environment individually (HOME-HAN and NOVEL-HAN, respectively); (iv) no-separation/no-handling (NON-SEP/NON-HAN) control condition, in which pups were left undisturbed in their home-cage. Compared to HOME-SEP rats, the NOVEL-SEP rats showed one day after the last MS enhanced stress-induced amygdala c-Fos expression and ACTH-release, despite of reduced adrenal corticosterone secretion. The higher amygdala c-Fos expression, ACTH-release and reduced corticosterone output observed postnatally, persisted into adulthood of the NOVEL-SEP animals. Behaviorally, NOVEL-SEP juvenile rats displayed deficits in social play, had intact spatial memory in the peri-pubertal period and showed more contextual fear memory compared to HOME-SEP in adulthood. Finally, NOVEL-HAN, compared to HOME-HAN, displayed increased stress-induced corticosterone output, no deficits in social play and reduced contextual fear. In conclusion, programming of an adult fearful phenotype linked to amygdala priming develops if pups are repeatedly isolated from peers in a novel-environment, while away from the dam for a prolonged period of time.
长时间的母体分离(MS)会激活新生儿的下丘脑-垂体-肾上腺轴,导致基础和应激诱导的皮质酮水平升高,这可能启动杏仁核依赖的恐惧学习。在这里,我们测试了一个假设,即成年期的恐惧表型是由幼崽在长时间的 MS 期间经历的应激所编程的,而不是由长时间的母体分离本身所编程的。为此,我们在新生后第 3 天(pnd3)对 Wistar 幼鼠进行了以下处理:(i)在家庭环境中反复分离(HOME-SEP),每天 8 小时分离 3 天,幼崽留在家庭笼中;(ii)在新环境中反复分离(NOVEL-SEP),采用相同的分离程序,但现在幼崽在 8 小时母鼠离开期间单独在新环境中饲养;(iii)反复处理,包括每天在家中或在新环境中进行短暂(15 分钟而不是 8 小时)的 MS(分别为 HOME-HAN 和 NOVEL-HAN);(iv)无分离/无处理(NON-SEP/NON-HAN)对照条件,幼鼠在其家庭笼中未被打扰。与 HOME-SEP 大鼠相比,NOVEL-SEP 大鼠在最后一次 MS 后一天显示出增强的应激诱导杏仁核 c-Fos 表达和 ACTH 释放,尽管肾上腺皮质酮分泌减少。NOVEL-SEP 动物在出生后观察到的更高的杏仁核 c-Fos 表达、ACTH 释放和降低的皮质酮输出持续到成年期。行为上,NOVEL-SEP 幼鼠在社交游戏中表现出缺陷,在青春期前期间具有完整的空间记忆,并且在成年期与 HOME-SEP 相比表现出更多的情境恐惧记忆。最后,与 HOME-HAN 相比,NOVEL-HAN 显示出应激诱导的皮质酮输出增加、社交游戏无缺陷和情境恐惧减少。总之,如果幼崽在新环境中与同伴长时间分离,同时与母鼠长时间分离,就会形成与杏仁核启动相关的成年期恐惧表型。