» Articles » PMID: 19359671

Posttraumatic Stress Disorder: the Role of Medial Prefrontal Cortex and Amygdala

Overview
Journal Neuroscientist
Publisher Sage Publications
Specialty Neurology
Date 2009 Apr 11
PMID 19359671
Citations 141
Authors
Affiliations
Soon will be listed here.
Abstract

Posttraumatic stress disorder (PTSD) is characterized by recurrent distressing memories of an emotionally traumatic event. In this review, the authors present neuroscientific data highlighting the function of two brain areas--the amygdala and ventromedial prefrontal cortex (vmPFC)--in PTSD and related emotional processes. A convergent body of human and nonhuman studies suggests that the amygdala mediates the acquisition and expression of conditioned fear and the enhancement of emotional memory, whereas the vmPFC mediates the extinction of conditioned fear and the volitional regulation of negative emotion. It has been theorized that the vmPFC exerts inhibition on the amygdala, and that a defect in this inhibition could account for the symptoms of PTSD. This theory is supported by functional imaging studies of PTSD patients, who exhibit hypoactivity in the vmPFC but hyperactivity in the amygdala. A recent study of brain-injured and trauma-exposed combat veterans confirms that amygdala damage reduces the likelihood of developing PTSD. But contrary to the prediction of the top-down inhibition model, vmPFC damage also reduces the likelihood of developing PTSD. The putative roles of the amygdala and the vmPFC in the pathophysiology of PTSD, as well as implications for potential treatments, are discussed in light of these results.

Citing Articles

Chronobiology in Paediatric Neurological and Neuropsychiatric Disorders: Harmonizing Care with Biological Clocks.

Giannotta G, Ruggiero M, Trabacca A J Clin Med. 2025; 13(24.

PMID: 39768659 PMC: 11678831. DOI: 10.3390/jcm13247737.


Accelerated development of cardiovascular risk factors mediates risk for major adverse cardiovascular events in posttraumatic stress disorder.

Khalil M, Sinnott S, Civieri G, Abohashem S, Grewal S, Hanlon E Brain Behav Immun. 2024; 125:148-157.

PMID: 39733862 PMC: 11903154. DOI: 10.1016/j.bbi.2024.12.155.


The Role of Implicit Memory in the Development and Recovery from Trauma-Related Disorders.

Damis L NeuroSci. 2024; 3(1):63-88.

PMID: 39484673 PMC: 11523743. DOI: 10.3390/neurosci3010005.


Time-dependent neural arbitration between cue associative and episodic fear memories.

Cortese A, Ohata R, Alemany-Gonzalez M, Kitagawa N, Imamizu H, Koizumi A Nat Commun. 2024; 15(1):8706.

PMID: 39433735 PMC: 11494204. DOI: 10.1038/s41467-024-52733-4.


Chronic Stress Alters Synaptic Inhibition/Excitation Balance of Pyramidal Neurons But Not PV Interneurons in the Infralimbic and Prelimbic Cortices of C57BL/6J Mice.

Rodrigues D, Santa C, Manadas B, Monteiro P eNeuro. 2024; 11(8).

PMID: 39147579 PMC: 11351013. DOI: 10.1523/ENEURO.0053-24.2024.


References
1.
Rosenkranz J, Moore H, Grace A . The prefrontal cortex regulates lateral amygdala neuronal plasticity and responses to previously conditioned stimuli. J Neurosci. 2003; 23(35):11054-64. PMC: 6741051. View

2.
Hampton A, Adolphs R, Tyszka M, ODoherty J . Contributions of the amygdala to reward expectancy and choice signals in human prefrontal cortex. Neuron. 2007; 55(4):545-55. DOI: 10.1016/j.neuron.2007.07.022. View

3.
Quirk G, Likhtik E, Pelletier J, Pare D . Stimulation of medial prefrontal cortex decreases the responsiveness of central amygdala output neurons. J Neurosci. 2003; 23(25):8800-7. PMC: 6740415. View

4.
Mayberg H, Lozano A, Voon V, McNeely H, Seminowicz D, Hamani C . Deep brain stimulation for treatment-resistant depression. Neuron. 2005; 45(5):651-60. DOI: 10.1016/j.neuron.2005.02.014. View

5.
Phelps E, Delgado M, Nearing K, LeDoux J . Extinction learning in humans: role of the amygdala and vmPFC. Neuron. 2004; 43(6):897-905. DOI: 10.1016/j.neuron.2004.08.042. View