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1.
Acta Neurochir (Wien) ; 149(3): 281-9, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17288002

ABSTRACT

BACKGROUND: The contribution of brain edema to brain swelling in cases of traumatic brain injury (TBI) remains a critical problem. We believe that inflammatory reactions may play a fundamental role in brain swelling following a head injury. Although possible roles of microglia activation and the release of mediators have been suggested, direct evidence of cellular immune reactivity in diffuse brain injury following closed head trauma is lacking. Accordingly, the objective of this study was to assess the temporal pattern of microglia activation and lymphocyte migration in an experimental model of TBI. METHOD: An impact acceleration TBI model was utilized to induce diffuse brain damage in adult Wistar rats. The animals were separated into three groups: unoperated controls, sham-operated controls and trauma group. At various times after TBI induction (5 min-24 h), rats were perfused transcardially. Sagittal brain sections were analyzed with immunohistochemical markers of CD3 to reveal the presence of T-lymphocytes, and by immunochemistry for the detection of CD11b to reveal microglia activation within the brain parenchyma. FINDINGS: In the control groups, scattered T-cells were found in the brain parenchyma. In the trauma group, TBI induced microglia activation and a transient biphasic T-cell infiltration of the brain parenchyma in all regions was found, beginning as early as 30 min post injury and reaching its maximum values at 45 min and 3 h after trauma induction. CONCLUSION: These results lead us to suggest that the acute response to severe head trauma with early edema formation is likely to be associated with inflammatory events which might be triggered by activated microglia and infiltrating lymphocytes. It is difficult to overestimate the clinical significance of these observations, as the early and targeted treatment of patients with severe head injuries with immunosuppressive medication may result in a far more favorable outcome.


Subject(s)
Brain Injuries/immunology , Head Injuries, Closed/immunology , Immunity, Cellular/immunology , Acceleration , Animals , Brain/immunology , Brain/pathology , Brain Edema/immunology , Brain Edema/pathology , Brain Injuries/pathology , CD11b Antigen/analysis , CD3 Complex/immunology , Disease Models, Animal , Head Injuries, Closed/pathology , Intracranial Pressure/physiology , Lymphocytosis/immunology , Lymphocytosis/pathology , Male , Microglia/immunology , Microglia/pathology , Rats , T-Lymphocytes/immunology , T-Lymphocytes/pathology
2.
Neurol Res ; 21(8): 742-54, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10596383

ABSTRACT

This study examines neuropsychological dysfunction after varying severities of the Impact Acceleration Model of diffuse traumatic brain injury. Adult rats (340 g-400 g) were divided into five groups, and exposed to varying degrees of Impact Acceleration Injury (1 m, 2 m, 2.1 m/500 g and second insult). After injury, animals were allowed to recover; acute neurological reflexes, beam walk score, beam balance score, inclined plane score, and Morris Water Maze score were then assessed at multiple time points. Injury of all severities caused significant motor and cognitive deficits. With milder injuries these effects were transient; however, with more severe injuries no recovery in function was seen. The addition of hypoxia and hypotension made a moderate injury worse than a severe injury. The acute neurological reflexes, the beam balance test and the inclined plane test distinguished between the more severely injured groups, but were affected less by mild injury. The beam walk test was sensitive to mild injury, but appeared unable to distinguish between the severe groups. The Morris Water Maze was sensitive for all injury groups, but appeared to adopt a different response profile with secondary insult. This study has for the first time characterized the degree of motor and cognitive deficits in rodents exposed to differing severities of Impact Acceleration Injury. These data confirm that the tests considered, and the Injury Model used, provide a useful system for the consideration of potential therapies which might ameliorate neuropsychological deficits in diffuse brain injury.


Subject(s)
Acceleration , Brain Injuries/physiopathology , Cognition/physiology , Motor Skills/physiology , Acute Disease , Animals , Behavior, Animal , Body Weight , Brain Injuries/mortality , Chronic Disease , Disease Models, Animal , Male , Maze Learning , Neuropsychological Tests , Postural Balance , Predictive Value of Tests , Rats , Rats, Sprague-Dawley , Reflex
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