Repetitive mild traumatic brain injury (rmTBI) is a major contributor to long-term neurological dysfunction, yet many preclinical models lack precise control and quantification of biomechanical forces across impacts. We developed a reproducible, closed-skull mouse model of rmTBI using a custom-built weight-drop apparatus featuring a solenoid-based rebound arrest system, integrated high-speed videography, and accelerometry to track head kinematics during impact. Adult male and female mice received either a single impact or nine daily impacts. Linear and angular acceleration data were analyzed alongside behavioral and histological outcomes. Our apparatus delivered consistent impact and velocity forces with minimal inter-subject variability. Additionally, the animals experienced consistent linear and angular acceleration as measured using high-speed video capture. These impacts did not cause skull fracture or acute vascular hemorrhage, but impacted animals had increased return of righting reflex (RoRR) time, consistent with mild, concussion-like symptoms. Behavioral testing revealed reduced performance of rmTBI-affected mice in an olfaction-mediated foraging task (buried food task), particularly at later timepoints, consistent with progressive olfactory impairment. Immunohistochemical analysis of Iba1 and CD68 in the brain demonstrated sex-dependent microglial activation, with males showing higher expression levels in both single- and nine-impact models. Among the brain regions investigated, microglial activation was most pronounced in the corpus callosum, neocortex, and olfactory tubercle. These findings underscore the importance of including sex as a biological variable in rmTBI research and support the utility of this model for probing injury thresholds, regional vulnerability, and potential therapeutic interventions in repetitive head trauma. Significance Statement Mild traumatic brain injuries (mTBIs) contribute long-term sensory, motor, and cognitive dysfunction. We developed a novel approach for delivering repetitive mTBIs (rmTBIs) to mice via a custom weight-drop apparatus. The device allows precise control over impact forces and enables quantification of linear and angular acceleration during each impact. We describe the apparatus, the forces delivered, and the kinematics experienced by lightly anesthetized mice. We measured behavioral and neuroinflammatory sequelae in the brains of rmTBI-exposed mice compared to controls. rmTBI-exposed animals showed impairment in the olfaction-mediated buried food task and evidence of microglial reactivity in multiple brain regions days-to-weeks following injury. The results demonstrate the utility of this approach for studying rmTBI-associated pathophysiology, and for testing therapies or interventions for rmTBI.
Anthony B. Crum (Thu,) studied this question.