John I Broussard1, Laura Acion1,2, Héctor De Jesús-Cortés3, Terry Yin3, Jeremiah K Britt3, Ramiro Salas1,4, Mauro Costa-Mattioli5, Claudia Robertson6, Andrew A Pieper3,7,8,9,10, David B Arciniegas1, Ricardo Jorge1,4. 1. a Beth K and Stuart C. Yudofsky Division of Neuropsychiatry , Baylor College of Medicine , Houston , TX , USA. 2. b Instituto de Cálculo, Facultad de Ciencias Exactas y Naturales , Universidad de Buenos Aires - CONICET , Buenos Aires , Argentina. 3. c Departments of Psychiatry , University of Iowa , Iowa City , IA , USA. 4. d Department of Veteran Affairs , Michael E DeBakey VA Medical Center , Houston TX , USA. 5. e Free Radical & Radiation Biology Program, Department of Radiation Oncology Holden Comprehensive Cancer Center , University of Iowa , Iowa City , IA , USA. 6. f Department of Neurosurgery , Baylor College of Medicine , Houston , TX , USA. 7. g Neurology , University of Iowa , Iowa City , IA , USA. 8. h Department of Neuroscience , Baylor College of Medicine , Houston , TX , USA. 9. i Department of Veterans Affairs , Carver College of Medicine, University of Iowa , Iowa City , IA , USA. 10. j Cornell Autism Research Program , Weill Cornell Medical College , New York , NY , USA.
Abstract
PRIMARY OBJECTIVE: Repeated traumatic brain injuries (rmTBI) are frequently associated with debilitating neuropsychiatric conditions such as cognitive impairment, mood disorders, and post-traumatic stress disorder. We tested the hypothesis that repeated mild traumatic brain injury impairs spatial memory and enhances anxiety-like behaviour. RESEARCH DESIGN: We used a between groups design using single (smTBI) or repeated (rmTBI) controlled cranial closed skull impacts to mice, compared to a control group. METHODS AND PROCEDURES: We assessed the effects of smTBI and rmTBI using measures of motor performance (Rotarod Test [RT]), anxiety-like behaviour (Elevated Plus Maze [EPM] and Open Field [OF] tests), and spatial memory (Morris Water Maze [MWM]) within 12 days of the final injury. In separate groups of mice, astrocytosis and microglial activation were assessed 24 hours after the final injury using GFAP and IBA-1 immunohistochemistry. MAIN OUTCOMES AND RESULTS: RmTBI impaired spatial memory in the MWM and increased anxiety-like behaviour in the EPM and OFT. In addition, rmTBI elevated GFAP and IBA-1 immunohistochemistry throughout the mouse brain. RmTBI produced astrocytosis and microglial activation, and elicited impaired spatial memory and anxiety-like behaviour. CONCLUSIONS: rmTBI produces acute cognitive and anxiety-like disturbances associated with inflammatory changes in brain regions involved in spatial memory and anxiety.
PRIMARY OBJECTIVE: Repeated traumatic brain injuries (rmTBI) are frequently associated with debilitating neuropsychiatric conditions such as cognitive impairment, mood disorders, and post-traumatic stress disorder. We tested the hypothesis that repeated mild traumatic brain injury impairs spatial memory and enhances anxiety-like behaviour. RESEARCH DESIGN: We used a between groups design using single (smTBI) or repeated (rmTBI) controlled cranial closed skull impacts to mice, compared to a control group. METHODS AND PROCEDURES: We assessed the effects of smTBI and rmTBI using measures of motor performance (Rotarod Test [RT]), anxiety-like behaviour (Elevated Plus Maze [EPM] and Open Field [OF] tests), and spatial memory (Morris Water Maze [MWM]) within 12 days of the final injury. In separate groups of mice, astrocytosis and microglial activation were assessed 24 hours after the final injury using GFAP and IBA-1 immunohistochemistry. MAIN OUTCOMES AND RESULTS:RmTBI impaired spatial memory in the MWM and increased anxiety-like behaviour in the EPM and OFT. In addition, rmTBI elevated GFAP and IBA-1 immunohistochemistry throughout the mouse brain. RmTBI produced astrocytosis and microglial activation, and elicited impaired spatial memory and anxiety-like behaviour. CONCLUSIONS:rmTBI produces acute cognitive and anxiety-like disturbances associated with inflammatory changes in brain regions involved in spatial memory and anxiety.
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