Your browser doesn't support javascript.
loading
Spatial Distribution of Neuropathology and Neuroinflammation Elucidate the Biomechanics of Fluid Percussion Injury.
Beitchman, Joshua A; Lifshitz, Jonathan; Harris, Neil G; Thomas, Theresa Currier; Lafrenaye, Audrey D; Hånell, Anders; Dixon, C Edward; Povlishock, John T; Rowe, Rachel K.
Afiliação
  • Beitchman JA; BARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Lifshitz J; Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona, USA.
  • Harris NG; Midwestern University, Glendale, Arizona, USA.
  • Thomas TC; BARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Lafrenaye AD; Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona, USA.
  • Hånell A; Arizona State University, Tempe, Arizona, USA.
  • Dixon CE; Phoenix VA Health Care System, Phoenix, Arizona, USA.
  • Povlishock JT; UCLA Brain Injury Research Center, Department of Neurosurgery, and Intellectual Development and Disabilities Research Center, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, USA.
  • Rowe RK; BARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
Neurotrauma Rep ; 2(1): 59-75, 2021.
Article em En | MEDLINE | ID: mdl-34223546
ABSTRACT
Diffuse brain injury is better described as multi-focal, where pathology can be found adjacent to seemingly uninjured neural tissue. In experimental diffuse brain injury, pathology and pathophysiology have been reported far more lateral than predicted by the impact site. We hypothesized that local thickening of the rodent skull at the temporal ridges serves to focus the intracranial mechanical forces experienced during brain injury and generate predictable pathology. We demonstrated local thickening of the skull at the temporal ridges using contour analysis on magnetic resonance imaging. After diffuse brain injury induced by midline fluid percussion injury (mFPI), pathological foci along the anterior-posterior length of cortex under the temporal ridges were evident acutely (1, 2, and 7 days) and chronically (28 days) post-injury by deposition of argyophilic reaction product. Area CA3 of the hippocampus and lateral nuclei of the thalamus showed pathological change, suggesting that mechanical forces to or from the temporal ridges shear subcortical regions. A proposed model of mFPI biomechanics suggests that injury force vectors reflect off the skull base and radiate toward the temporal ridge, thereby injuring ventral thalamus, dorsolateral hippocampus, and sensorimotor cortex. Surgically thinning the temporal ridge before injury reduced injury-induced inflammation in the sensorimotor cortex. These data build evidence for temporal ridges of the rodent skull to contribute to the observed pathology, whether by focusing extracranial forces to enter the cranium or intracranial forces to escape the cranium. Pre-clinical investigations can take advantage of the predicted pathology to explore injury mechanisms and treatment efficacy.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article