TY - JOUR
T1 - Stress and fear extinction
AU - Maren, Stephen
AU - Holmes, Andrew
N1 - AH is supported by the NIAAA Intramural Research Program, Henry Jackson Foundation for the Advancement of Military Medicine, and the Department of Defense in the Center for Neuroscience and Regenerative Medicine. SM is supported by grants from the NIH (R01MH065961) and a McKnight Foundation Memory and Cognitive Disorders Award.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Stress has a critical role in the development and expression of many psychiatric disorders, and is a defining feature of posttraumatic stress disorder (PTSD). Stress also limits the efficacy of behavioral therapies aimed at limiting pathological fear, such as exposure therapy. Here we examine emerging evidence that stress impairs recovery from trauma by impairing fear extinction, a form of learning thought to underlie the suppression of trauma-related fear memories. We describe the major structural and functional abnormalities in brain regions that are particularly vulnerable to stress, including the amygdala, prefrontal cortex, and hippocampus, which may underlie stress-induced impairments in extinction. We also discuss some of the stress-induced neurochemical and molecular alterations in these brain regions that are associated with extinction deficits, and the potential for targeting these changes to prevent or reverse impaired extinction. A better understanding of the neurobiological basis of stress effects on extinction promises to yield novel approaches to improving therapeutic outcomes for PTSD and other anxiety and trauma-related disorders.
AB - Stress has a critical role in the development and expression of many psychiatric disorders, and is a defining feature of posttraumatic stress disorder (PTSD). Stress also limits the efficacy of behavioral therapies aimed at limiting pathological fear, such as exposure therapy. Here we examine emerging evidence that stress impairs recovery from trauma by impairing fear extinction, a form of learning thought to underlie the suppression of trauma-related fear memories. We describe the major structural and functional abnormalities in brain regions that are particularly vulnerable to stress, including the amygdala, prefrontal cortex, and hippocampus, which may underlie stress-induced impairments in extinction. We also discuss some of the stress-induced neurochemical and molecular alterations in these brain regions that are associated with extinction deficits, and the potential for targeting these changes to prevent or reverse impaired extinction. A better understanding of the neurobiological basis of stress effects on extinction promises to yield novel approaches to improving therapeutic outcomes for PTSD and other anxiety and trauma-related disorders.
UR - https://www.scopus.com/pages/publications/84949552491
UR - https://www.scopus.com/pages/publications/84949552491#tab=citedBy
U2 - 10.1038/npp.2015.180
DO - 10.1038/npp.2015.180
M3 - Review article
C2 - 26105142
AN - SCOPUS:84949552491
SN - 0893-133X
VL - 41
SP - 58
EP - 79
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 1
ER -