TY - JOUR
T1 - Juvenile traumatic brain injury evolves into a chronic brain disorder
T2 - Behavioral and histological changes over 6months
AU - Kamper, Joel E.
AU - Pop, Viorela
AU - Fukuda, Andrew M.
AU - Ajao, David O.
AU - Hartman, Richard E.
AU - Badaut, Jérôme
N1 - Funding Information:
The authors thank Dr. Andre Obenaus, Ms. Jacqueline Coats, Mr. Sonny Kim, and Mr. Kamal Ambadipudi for technical help in collecting MRI data. This work was supported in part by the NIH R01HD061946 (to JB) and the Swiss Science Foundation ( FN 31003A-122166 , to JB)
PY - 2013/12
Y1 - 2013/12
N2 - Traumatic brain injury (TBI) refers to physical trauma to the brain that can lead to motor and cognitive dysfunctions. TBI is particularly serious in infants and young children, often leading to long-term functional impairments. Although clinical research is useful for quantifying and observing the effects of these injuries, few studies have empirically assessed the long-term effects of juvenile TBI (jTBI) on behavior and histology. After a controlled cortical impact delivered to postnatal 17. day old rats, functional abilities were measured after 3, 5, and 6. months using open field (activity levels), zero maze (anxiety-like behaviors), rotarod (sensorimotor abilities, coordination, and balance), and water maze (spatial learning and memory, swim speed, turn bias). Sensorimotor function was impaired for up to 6. months in jTBI animals, which showed no improvement from repeated test exposure. Although spatial learning was not impaired, spatial memory deficits were observed in jTBI animals starting at 3. months after injury. Magnetic resonance imaging and histological data revealed that the effects of jTBI were evolving for up to 6. months post-injury, with reduced cortical thickness, decreased corpus callosum area and CA1 neuronal cell death in jTBI animals distant to the impact site. These findings suggest that this model of jTBI produces long-term impairments comparable to those reported clinically. Although some deficits were stable over time, the variable nature of other deficits (e.g., memory) as well as changing properties of the lesion itself, suggest that the effects of a single jTBI produce a chronic brain disorder with long-term complications.
AB - Traumatic brain injury (TBI) refers to physical trauma to the brain that can lead to motor and cognitive dysfunctions. TBI is particularly serious in infants and young children, often leading to long-term functional impairments. Although clinical research is useful for quantifying and observing the effects of these injuries, few studies have empirically assessed the long-term effects of juvenile TBI (jTBI) on behavior and histology. After a controlled cortical impact delivered to postnatal 17. day old rats, functional abilities were measured after 3, 5, and 6. months using open field (activity levels), zero maze (anxiety-like behaviors), rotarod (sensorimotor abilities, coordination, and balance), and water maze (spatial learning and memory, swim speed, turn bias). Sensorimotor function was impaired for up to 6. months in jTBI animals, which showed no improvement from repeated test exposure. Although spatial learning was not impaired, spatial memory deficits were observed in jTBI animals starting at 3. months after injury. Magnetic resonance imaging and histological data revealed that the effects of jTBI were evolving for up to 6. months post-injury, with reduced cortical thickness, decreased corpus callosum area and CA1 neuronal cell death in jTBI animals distant to the impact site. These findings suggest that this model of jTBI produces long-term impairments comparable to those reported clinically. Although some deficits were stable over time, the variable nature of other deficits (e.g., memory) as well as changing properties of the lesion itself, suggest that the effects of a single jTBI produce a chronic brain disorder with long-term complications.
KW - Behavior
KW - MRI
KW - Neurodegeneration
KW - Pediatric
KW - Traumatic brain injury
UR - https://www.scopus.com/pages/publications/84885336382
UR - https://www.scopus.com/pages/publications/84885336382#tab=citedBy
U2 - 10.1016/j.expneurol.2013.09.016
DO - 10.1016/j.expneurol.2013.09.016
M3 - Article
C2 - 24076005
SN - 0014-4886
VL - 250
SP - 8
EP - 19
JO - Experimental Neurology
JF - Experimental Neurology
ER -