TY - JOUR
T1 - Early Life Adversity and Neuropsychiatric Disease
T2 - Differential Outcomes and Translational Relevance of Rodent Models
AU - Waters, Renée C.
AU - Gould, Elizabeth
N1 - Funding Information:
This work was funded by NIMH grant R01MH117459-01 to EG and NSF GRFP 2021318039 to RW.
Publisher Copyright:
Copyright © 2022 Waters and Gould.
PY - 2022/6/23
Y1 - 2022/6/23
N2 - 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.
AB - 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.
KW - PTSD
KW - amygdala
KW - animal models
KW - anxiety disorders
KW - childhood maltreatment
KW - hippocampus
KW - major depressive disorder
KW - prefrontal cortex
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U2 - 10.3389/fnsys.2022.860847
DO - 10.3389/fnsys.2022.860847
M3 - Review article
AN - SCOPUS:85133826252
SN - 1662-5137
VL - 16
JO - Frontiers in Systems Neuroscience
JF - Frontiers in Systems Neuroscience
M1 - 860847
ER -