4.2 Review

Early Life Adversity and Neuropsychiatric Disease: Differential Outcomes and Translational Relevance of Rodent Models

期刊

FRONTIERS IN SYSTEMS NEUROSCIENCE
卷 16, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnsys.2022.860847

关键词

childhood maltreatment; anxiety disorders; major depressive disorder; PTSD; animal models; hippocampus; prefrontal cortex; amygdala

资金

  1. NIMH [R01MH117459-01]
  2. NSF [GRFP 2021318039]

向作者/读者索取更多资源

It has been well-established that early life adversity (ELA) predisposes individuals to develop various neuropsychiatric conditions. This review first investigates the different types of ELA that may contribute to changes in the human brain and subsequent neuropsychiatric outcomes. It then evaluates the translational relevance of rodent models of ELA in understanding the links between specific experiences and dysfunctions in neural circuits.
It is now well-established that early life adversity (ELA) predisposes individuals to develop several neuropsychiatric conditions, including anxiety disorders, and major depressive disorder. However, ELA is a very broad term, encompassing multiple types of negative childhood experiences, including physical, sexual and emotional abuse, physical and emotional neglect, as well as trauma associated with chronic illness, family separation, natural disasters, accidents, and witnessing a violent crime. Emerging literature suggests that in humans, different types of adverse experiences are more or less likely to produce susceptibilities to certain conditions that involve affective dysfunction. To investigate the driving mechanisms underlying the connection between experience and subsequent disease, neuroscientists have developed several rodent models of ELA, including pain exposure, maternal deprivation, and limited resources. These studies have also shown that different types of ELA paradigms produce different but somewhat overlapping behavioral phenotypes. In this review, we first investigate the types of ELA that may be driving different neuropsychiatric outcomes and brain changes in humans. We next evaluate whether rodent models of ELA can provide translationally relevant information regarding links between specific types of experience and changes in neural circuits underlying dysfunction.

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