Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes

Chronic exposure to uncontrollable stress causes loss of spines and dendrites in the prefrontal cortex (PFC), a recently evolved brain region that provides top-down regulation of thought, action, and emotion. PFC neurons generate top-down goals through recurrent excitatory connections on spines. Thi...

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Main Authors: Elizabeth Woo, Lauren H. Sansing, Amy F. T. Arnsten, Dibyadeep Datta
Format: Article
Language:English
Published: SAGE Publishing 2021-08-01
Series:Chronic Stress
Online Access:https://doi.org/10.1177/24705470211029254
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spelling doaj-0109f887b8b0494fbb829ad6c32705862021-08-30T21:33:19ZengSAGE PublishingChronic Stress2470-54702021-08-01510.1177/24705470211029254Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular ChangesElizabeth WooLauren H. SansingAmy F. T. ArnstenDibyadeep DattaChronic exposure to uncontrollable stress causes loss of spines and dendrites in the prefrontal cortex (PFC), a recently evolved brain region that provides top-down regulation of thought, action, and emotion. PFC neurons generate top-down goals through recurrent excitatory connections on spines. This persistent firing is the foundation for higher cognition, including working memory, and abstract thought. However, exposure to acute uncontrollable stress drives high levels of catecholamine release in the PFC, which activates feedforward calcium-cAMP signaling pathways to open nearby potassium channels, rapidly weakening synaptic connectivity to reduce persistent firing. Chronic stress exposures can further exacerbate these signaling events leading to loss of spines and resulting in marked cognitive impairment. In this review, we discuss how stress signaling mechanisms can lead to spine loss, including changes to BDNF-mTORC1 signaling, calcium homeostasis, actin dynamics, and mitochondrial actions that engage glial removal of spines through inflammatory signaling. Stress signaling events may be amplified in PFC spines due to cAMP magnification of internal calcium release. As PFC dendritic spine loss is a feature of many cognitive disorders, understanding how stress affects the structure and function of the PFC will help to inform strategies for treatment and prevention.https://doi.org/10.1177/24705470211029254
collection DOAJ
language English
format Article
sources DOAJ
author Elizabeth Woo
Lauren H. Sansing
Amy F. T. Arnsten
Dibyadeep Datta
spellingShingle Elizabeth Woo
Lauren H. Sansing
Amy F. T. Arnsten
Dibyadeep Datta
Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes
Chronic Stress
author_facet Elizabeth Woo
Lauren H. Sansing
Amy F. T. Arnsten
Dibyadeep Datta
author_sort Elizabeth Woo
title Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes
title_short Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes
title_full Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes
title_fullStr Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes
title_full_unstemmed Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes
title_sort chronic stress weakens connectivity in the prefrontal cortex: architectural and molecular changes
publisher SAGE Publishing
series Chronic Stress
issn 2470-5470
publishDate 2021-08-01
description Chronic exposure to uncontrollable stress causes loss of spines and dendrites in the prefrontal cortex (PFC), a recently evolved brain region that provides top-down regulation of thought, action, and emotion. PFC neurons generate top-down goals through recurrent excitatory connections on spines. This persistent firing is the foundation for higher cognition, including working memory, and abstract thought. However, exposure to acute uncontrollable stress drives high levels of catecholamine release in the PFC, which activates feedforward calcium-cAMP signaling pathways to open nearby potassium channels, rapidly weakening synaptic connectivity to reduce persistent firing. Chronic stress exposures can further exacerbate these signaling events leading to loss of spines and resulting in marked cognitive impairment. In this review, we discuss how stress signaling mechanisms can lead to spine loss, including changes to BDNF-mTORC1 signaling, calcium homeostasis, actin dynamics, and mitochondrial actions that engage glial removal of spines through inflammatory signaling. Stress signaling events may be amplified in PFC spines due to cAMP magnification of internal calcium release. As PFC dendritic spine loss is a feature of many cognitive disorders, understanding how stress affects the structure and function of the PFC will help to inform strategies for treatment and prevention.
url https://doi.org/10.1177/24705470211029254
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