%0 Journal Article %T Different forms of traumatic brain injuries cause different tactile hypersensitivity profiles %J Pain %D 2020 %A Wattiez, Anne-Sophie %A Castonguay, William C. %A Gaul, Olivia J. %A Waite, Jayme S. %A Schmidt, Chantel M. %A Reis, Alyssa S. %A Rea, Brandon J. %A Sowers, Levi P. %A Cintrón-Pérez, Coral J. %A Vázquez-Rosa, Edwin %A Pieper, Andrew A. %A Russo, Andrew F. %V ePub %N ePub %P ePub-ePub %X Chronic complications of traumatic brain injury (TBI) represent one of the greatest financial burdens and sources of suffering in society today. A substantial number of these patients suffer from post-traumatic headache (PTH), which is typically associated with tactile allodynia. Unfortunately, this phenomenon has been under-studied, in large part due to the lack of well-characterized laboratory animal models. We have addressed this gap in the field by characterizing the tactile sensory profile of two non-penetrating models of PTH. We show that multimodal TBI, administered by a jet-flow overpressure chamber that delivers a severe compressive impulse accompanied by a variable shock front and acceleration-deceleration insult, produces long term tactile hypersensitivity and widespread sensitization. These are phenotypes reminiscent of PTH in patients, in both cephalic and extracephalic regions. By contrast, closed head injury induces only transient cephalic tactile hypersensitivity, with no extracephalic consequences. Both models show a more severe phenotype with repetitive daily injury for three days, compared to either one or three successive injuries in a single day, providing new insight into patterns of injury that may place patients at greater risk of developing PTH. After recovery from transient cephalic tactile hypersensitivity, mice subjected to closed head injury demonstrate persistent hypersensitivity to established migraine triggers, including calcitonin gene-related peptide (CGRP) and sodium nitroprusside, a nitric oxide donor. Our results offer the field new tools for studying PTH, as well as preclinical support for a pathophysiologic role of CGRP in this condition.

Language: en

%G en %I Lippincott, Williams and Wilkins %@ 0304-3959 %U http://dx.doi.org/10.1097/j.pain.0000000000002103