Prenatal stress induces spatial memory deficits and epigenetic changes in the hippocampus indicative of heterochromatin formation and reduced gene expression

被引:76
作者
Benoit, Jamie D. [1 ]
Rakic, Pasko [2 ]
Frick, Karyn M. [3 ]
机构
[1] Yale Univ, Dept Psychol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06520 USA
[3] Univ Wisconsin, Dept Psychol, Milwaukee, WI 53211 USA
关键词
Chronic unpredictable stress; Sex differences; Mouse; Morris water maze; Histone acetylation; DNA methyltransferase; LONG-TERM-MEMORY; DNA METHYLATION; HISTONE ACETYLATION; SYNAPTIC PLASTICITY; OBJECT-LOCATION; RATS; INHIBITION; EXPOSURE; BEHAVIOR; SEX;
D O I
10.1016/j.bbr.2014.12.001
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Stress during pregnancy has a wide variety of negative effects in both human [1] and animal offspring [2]. These effects are especially apparent in various forms of learning and memory such as object recognition [3] and spatial memory [4]. The cognitive effects of prenatal stress (PNS) may be mediated through epigenetic changes such as histone acetylation and DNA methylation [5]. As such, the present study investigated the effects of chronic unpredictable PNS on memory and epigenetic measures in adult offspring. Mice that underwent PNS exhibited impaired spatial memory in the Morris water maze, as well as sex-specific changes in levels of DNA methyltransferase (DNMT) 1 protein, and acetylated histone H3 (AcH3) in the hippocampus, and serum corticosterone. Male mice exposed to PNS exhibited decreased hippocampal AcH3, whereas female PNS mice displayed a further reduction in AcH3, as well as heightened hippocampal DNMT1 protein levels and corticosterone levels. These data suggest that PNS may epigenetically reduce transcription in the hippocampus, particularly in females in whom this effect may be related to increased baseline stress hormone levels, and which may underlie the sexual dimorphism in rates of mental illness in humans. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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