The effects of trauma on brain and body: A unifying role for the midbrain periaqueductal gray. Issue 9 (28th June 2019)

• Record Type: Journal Article
• Authors: Terpou, Braeden A.; Harricharan, Sherain; McKinnon, Margaret C.; Frewen, Paul; Jetly, Rakesh; Lanius, Ruth A.
• Is Part Of: Journal of neuroscience research. Volume 97:Issue 9(2019)
• Page Start: 1110
• Page End: 1140
• Publication Date: 2019-06-28
• Subjects: brainstem -- dissociation -- periaqueductal gray -- PTSD -- trauma; Neurobiology -- Periodicals; 612
• DOI: 10.1002/jnr.24447
• Languages: English
• ISSNs: 0360-4012

Abstract

Abstract: Post‐traumatic stress disorder (PTSD), a diagnosis that may follow the experience of trauma, has multiple symptomatic phenotypes. Generally, individuals with PTSD display symptoms of hyperarousal and of hyperemotionality in the presence of fearful stimuli. A subset of individuals with PTSD; however, elicit dissociative symptomatology (i.e., depersonalization, derealization) in the wake of a perceived threat. This pattern of response characterizes the dissociative subtype of the disorder, which is often associated with emotional numbing and hypoarousal. Both symptomatic phenotypes exhibit attentional threat biases, where threat stimuli are processed preferentially leading to a hypervigilant state that is thought to promote defensive behaviors during threat processing. Accordingly, PTSD and its dissociative subtype are thought to differ in their proclivity to elicit active (i.e., fight, flight) versus passive (i.e., tonic immobility, emotional shutdown) defensive responses, which are characterized by the increased and the decreased expression of the sympathetic nervous system, respectively. Moreover, active and passive defenses are accompanied by primarily endocannabinoid‐ and opioid‐mediated analgesics, respectively. Through critical review of the literature, we apply the defense cascade model to better understand the pathological presentation of defensive responses in PTSD with a focus on the functioning of lower‐level midbrain and extended brainstem systems.