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A common denominator: PTSD, rapid eye movements, and fear extinction (Proceedings of the National Academy of Sciences of the United States of America)

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Home / Resources / PTSD / A common denominator: PTSD, rapid eye movements, and fear extinction (Proceedings of the National Academy of Sciences of the United States of America)

A common denominator: PTSD, rapid eye movements, and fear extinction

An observation and inquiry into research about neural pathways of fear extinction and PTSD with impacts on EMDR mechanisms of action.


Letter

“The work of Zhang et al. is at the fulcrum of a number of lines of research (1). There is a missing piece in the physiological puzzle the authors must report. The authors observe that dopaminergic neuronal stimuli from the ventral tegmental area (VTA) to the basolateral amygdala (BLA) are germane to fear extinction and thus potentially its impediment in conditions such as posttraumatic stress disorder (PTSD). However, the VTA to BLA neuronal route is the exact same pathway that elicits rapid eye movements in rapid eye movement (REM) sleep (2). This is critically important. In the treatment of PTSD, a current therapy known as eye movement desensitization and reprocessing therapy involves encouraging the participant to effect bilateral eye movements, akin to those during REM sleep while focusing on the distressing experience (3). It has been shown to be effective and is recommended by World Health Organisation and United Kingdom National Institute for Health and Care Excellence; however, the exact mechanism remains unclear (4). REM sleep is critical to processing traumatic events (5). Zhang et al. show a potential neuronal basis for this. It is important to determine from the study if the neuronal stimulation resulted in any increase or change in eye movements in the murine subjects. This information would be instrumental in the further elucidation of the mechanisms that belie fear extinction and pathologies and therapeutic interventions thereof.

Letter refers to this article: 

Zhang, X., Flick, K., Rizzo, M., & Tonegawa, S. (2025). Dopamine induces fear extinction by activating the reward-responding amygdala neurons. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 122(18), e2501331122. Open access: https://doi.org/10.1073/pnas.2501331122

  • Significance: The ability to extinguish fearful associations that are no longer relevant is crucial for survival. Understanding the neural circuits and neuromodulators that regulate fear extinction is necessary to improve treatment for many fear-related mental health disorders, like posttraumatic stress disorder (PTSD). New extinction memory is formed and stored in the basolateral amygdala (BLA). However, it has been unknown how the extinction learning is initiated in the BLA. Here, through a combination of in vivo dopamine recordings and functional manipulations, we show that dopamine acts differentially on distinct BLA subpopulations to control fear extinction learning.”

—Description from publisher

Letter Access

Open Access

Uzoigwe, C. E. (2025). A common denominator: PTSD, rapid eye movements, and fear extinction. Letter in Proceedings of the National Academy of Sciences of the United States of America (PNAS), 122(32), e2511191122. Open access: https://doi.org/10.1073/pnas.2511191122

View the Resource
Basic Info Collapse

Date
August 4, 2025

Creator(s)
Chika Edward Uzoigwe

Topics
PTSD

Practice & Methods
Mechanisms of Action, Neurobiology

More Info Collapse

Extent
1 page

Publisher
Proceedings of the National Academy of Sciences of the United States of America

Rights
Copyright © 2025 the Author(s).

APA Citation
Uzoigwe, C. E. (2025). A common denominator: PTSD, rapid eye movements, and fear extinction. Letter in Proceedings of the National Academy of Sciences of the United States of America (PNAS), 122(32), e2511191122. Open access: https://doi.org/10.1073/pnas.2511191122

Audience
EMDR Therapists, Other Mental Health Professionals

Language
English

Content Type
Article, Peer-Reviewed

Access Type
External Resource, Open Access

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