A mouse model of human repetitive mild traumatic brain injury

• Published in: Journal of neuroscience methods Vol. 203; no. 1; pp. 41 - 49
• Main Authors: Kane, Michael J., Angoa-Pérez, Mariana, Briggs, Denise I., Viano, David C., Kreipke, Christian W., Kuhn, Donald M.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15.01.2012
• Subjects: Animals; Brain Injuries - metabolism; Brain Injuries - pathology; Concussive; Disease Models, Animal; Glial Fibrillary Acidic Protein; Head acceleration; Humans; Immunoblotting; Immunohistochemistry; Mice; Mild; Nerve Tissue Proteins - analysis; Nerve Tissue Proteins - metabolism; Recovery of Function; Repetitive; Tauopathy; Traumatic brain injury; Mild; Traumatic brain injury; Head acceleration; Concussive; Tauopathy; Repetitive
• DOI: 10.1016/j.jneumeth.2011.09.003
• ISSN: 0165-0270; 1872-678X

► Development of a new model of human repetitive mild TBI using mice as subjects. ► Method can be used repetitively to impart diffuse closed-head injury without causing skull fracture, intracranial bleeding or seizures. ► Neurological and behavioral effects are mild and show recovery over time. ► Histopathological findings are consistent with analysis of postmortem human brains from individuals suffering multiple, mild concussive injuries. ► Model overcomes constraints on existing animal models of TBI to allow characterization of the pathophysiology of repetitive mild TBI. A novel method for the study of repetitive mild traumatic brain injury (rmTBI) that models the most common form of head injury in humans is presented. Existing animal models of TBI impart focal, severe damage unlike that seen in repeated and mild concussive injuries, and few are configured for repetitive application. Our model is a modification of the Marmarou weight drop method and allows repeated head impacts to lightly anesthetized mice. A key facet of this method is the delivery of an impact to the cranium of an unrestrained subject allowing rapid acceleration of the free-moving head and torso, an essential characteristic known to be important for concussive injury in humans, and a factor that is missing from existing animal models of TBI. Our method does not require scalp incision, emplacement of protective skull helmets or surgery and the procedure can be completed in 1–2min. Mice spontaneously recover the righting reflex and show no evidence of seizures, paralysis or impaired behavior. Skull fractures and intracranial bleeding are very rare. Minor deficits in motor coordination and locomotor hyperactivity recover over time. Histological analyses reveal mild astrocytic reactivity (increased expression of GFAP) and increased phospho-tau but a lack of blood–brain-barrier disruption, edema and microglial activation. This new animal model is simple and cost-effective and will facilitate characterization of the neurobiological and behavioral consequences of rmTBI. It is also ideal for high throughput screening of potential new therapies for mild concussive injuries as experienced by athletes and military personnel.