Stress in utero alters neonatal stress-induced regulation of the synaptic plasticity proteins Arc and Egr1 in a sex-specific manner

被引:17
作者
Groeger, Nicole [1 ]
Bock, Joerg [1 ,2 ]
Goehler, Daniela [1 ]
Blume, Nicole [3 ]
Lisson, Nicole [3 ]
Poeggel, Gerd [3 ]
Braun, Katharina [1 ,2 ]
机构
[1] Univ Magdeburg, Dept Zool Dev Neurobiol, Inst Biol, Leipziger Str 44, D-39120 Magdeburg, Germany
[2] CBBS, Magdeburg, Germany
[3] Univ Leipzig, Inst Biol, Human Biol, Talstr 33, D-04103 Leipzig, Germany
关键词
Immediate early genes; Epigenetic; Brain development; Quantitative immunocytochemistry; Hippocampal formation; Resilience; PRENATAL STRESS; PREFRONTAL CORTEX; FEMALE RATS; MATERNAL-DEPRIVATION; DENDRITIC COMPLEXITY; SPINE DENSITY; MOUSE MODEL; GENES ARC; HIPPOCAMPUS; EXPERIENCE;
D O I
10.1007/s00429-014-0889-3
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The present study in juvenile rats investigated a "two-hit model" to test the impact of prenatal stress exposure ("first hit") on the regulation of the synaptic plasticity immediate early genes Arc and Egr1 in response to a second neonatal stressor ("second hit") in a sex-specific manner. Three stress-exposed animal groups were compared at the age of 21 days in relation to unstressed controls (CON): preS animals were exposed to various unpredictable stressors during the last gestational trimester; postS animals were exposed to 45 min restraint stress at postnatal day 21, pre/postS animals were exposed to a combination of pre- and postnatal stress as described for the two previous groups. The postS and pre/postS groups were killed 2 h after exposure to the postnatal stressor, males and females were separately analyzed. In line with our hypothesis we detected sex-specific stress sensitivity for both analyzed proteins. Males did not show any significant changes in Arc expression irrespective of the stress condition. In contrast, females, which had been pre-exposed to prenatal stress, displayed an "amplified" Arc upregulation in response to postnatal stress (pre/postS group) compared to unstressed controls, which may reflect a "sensitization" effect of prenatal stress. For Egr1, the females did not show any stress-induced regulation irrespective of the stress condition, whereas in males, which were pre-exposed to prenatal stress, we observed a "protective" effect of prenatal stress on postnatal stress-induced downregulation of Egr1 expression (pre/postS group), which may indicate that prenatal stress exposure may induce "resilience".
引用
收藏
页码:679 / 685
页数:7
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