• Abigail G Schindler, Garth E Terry, Tami Wolden-Hanson, Marcella Cline, Michael Park, Janet Lee, Mayumi Yagi, James S Meabon, Elaine R Peskind, Murray M Raskind, PhillipsPaul E MPEMDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.Graduate Program in Neuroscience, University of Washington, Seattle, Washington, USA.Department of Pharmacology, University of Washingt, and David G Cook.
• Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
• J. Neurotrauma. 2021 Apr 1; 38 (7): 940948940-948.

AbstractRepetitive mild traumatic brain injury (mTBI) has been called the "signature injury" of military service members in the Iraq and Afghanistan wars and is highly comorbid with post-traumatic stress disorder (PTSD). Correct attribution of adverse blast-induced mTBI and/or PTSD remains challenging. Pre-clinical research using animal models can provide important insight into the mechanisms by which blast produces injury and dysfunction-but only to the degree by which such models reflect the human experience. Avoidance of trauma reminders is a hallmark of PTSD. Here, we sought to understand whether a mouse model of blast reproduces this phenomenon, in addition to blast-induced physical injuries. Drawing on well-established work from the chronic stress and Pavlovian conditioning literature, we hypothesized that even while one is anesthetized during blast exposure, environmental cues encountered in the peri-blast environment could be conditioned to evoke aversion/dysphoria and re-experiencing of traumatic stress. Using a pneumatic shock tube that recapitulates battlefield-relevant open-field blast forces, we provide direct evidence that stress is inherent to repetitive blast exposure, resulting in chronic aversive/dysphoric-like responses to previous blast-paired cues. The results in this report demonstrate that, although both single and repetitive blast exposures produce acute stress responses (weight loss, corticosterone increase), only repetitive blast exposure also results in co-occurring aversive/dysphoric-like stress responses. These results extend appreciation of the highly complex nature of repetitive blast exposure; and lend further support for the potential translational relevance of animal modeling approaches currently used by multiple laboratories aimed at elucidating the mechanisms (both molecular and behavioral) of repetitive blast exposure.

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