CHRONIC STRESS INDUCES PERSISTENT CHANGES IN GLOBAL DNA METHYLATION AND GENE EXPRESSION IN THE MEDIAL PREFRONTAL CORTEX, ORBITOFRONTAL CORTEX, AND HIPPOCAMPUS

被引:38
作者
Mychasiuk, R. [1 ]
Muhammad, A. [2 ]
Kolb, B. [2 ]
机构
[1] Univ Calgary, Alberta Childrens Hosp, Res Inst, Calgary, AB T2N 1N4, Canada
[2] Univ Lethbridge, Canadian Ctr Behav Neurosci, Lethbridge, AB T1K 3M4, Canada
关键词
RNA sequencing; Ingenuity Pathway Analysis; Long-Evans rats; neuronal morphology; epigenetic; DENDRITIC MORPHOLOGY; SEX-DIFFERENCES; PLASTICITY; ALIGNMENT; BRAIN; AXIS;
D O I
10.1016/j.neuroscience.2016.02.053
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chronic stress is associated with a plethora of cognitive symptoms such as emotional dysregulation and impaired executive function that have been attributed to modifications in neuroanatomy in the orbitofrontal cortex (OFC), medial prefrontal cortex (mPFC), and hippocampus (HPC). While many studies have examined stress-induced changes in neuronal morphology, synaptic plasticity, and cellular function, there has been little investigation into persistent changes in gene expression that may be responsible for the maintenance of these changes. This study exposed adult rats to a chronic stressor and then examined changes in mRNA gene expression in the OFC, mPFC and HPC following a two-week withdrawal period. mRNA bio-sequencing results revealed sex-and region-dependent changes. Surprisingly the greatest changes in gene expression were found in the OFC, and similar to anatomical studies, analysis of gene changes with Ingenuity Pathway Analysis software demonstrated that the mPFC and OFC exhibited contrasting activation of canonical pathways and functional networks. The HPC demonstrated the largest degree of sex-dependent change in gene expression. In general, chronic stress induced persistent changes in gene expression in the three brain regions we examined and these changes could be associated with the commonly reported cognitive symptoms. The current study highlights the region-and sex-dependent nature of the brain's response to chronic stress and the difficulty we face when attempting to develop treatment options. (C) 2016 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:489 / 499
页数:11
相关论文
共 43 条
[1]   NMDA receptor regulation by Src kinase signalling in excitatory synaptic transmission and plasticity [J].
Ali, DW ;
Salter, MW .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :336-342
[2]   Differential expression analysis for sequence count data [J].
Anders, Simon ;
Huber, Wolfgang .
GENOME BIOLOGY, 2010, 11 (10)
[3]   The effects of stress exposure on prefrontal cortex: Translating basic research into successful treatments for post-traumatic stress disorder [J].
Arnsten, Amy F. T. ;
Raskind, Murray A. ;
Taylor, Fletcher B. ;
Connor, Daniel F. .
NEUROBIOLOGY OF STRESS, 2015, 1 :89-99
[4]   Stress signalling pathways that impair prefrontal cortex structure and function [J].
Arnsten, Amy F. T. .
NATURE REVIEWS NEUROSCIENCE, 2009, 10 (06) :410-422
[5]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[6]  
Catalina-Rodriguez O, 2012, ONCOTARGET, V3, P1220
[7]   Peroxisome proliferator-activated receptors (PPARs): Nuclear receptors at the crossroads between lipid metabolism and inflammation [J].
Chinetti, G ;
Fruchart, JC ;
Staels, B .
INFLAMMATION RESEARCH, 2000, 49 (10) :497-505
[8]   The synucleins: a family of proteins involved in synaptic function, plasticity, neurodegeneration and disease [J].
Clayton, DF ;
George, JM .
TRENDS IN NEUROSCIENCES, 1998, 21 (06) :249-254
[9]   Psychological stress and disease [J].
Cohen, Sheldon ;
Janicki-Deverts, Denise ;
Miller, Gregory E. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 298 (14) :1685-1687
[10]   The brain and the stress axis: The neural correlates of cortisol regulation in response to stress [J].
Dedovic, Katarina ;
Duchesne, Annie ;
Andrews, Julie ;
Engert, Veronika ;
Pruessner, Jens C. .
NEUROIMAGE, 2009, 47 (03) :864-871