Repeated mild traumatic brain injury in female rats increases lipid peroxidation in neurons
Negative outcomes of mild traumatic brain injury (mTBI) can be exacerbated by repeated insult. Animal models of repeated closed-head mTBI provide the opportunity to define acute pathological mechanisms as the number of mTBI increases. Furthermore, little is known about the effects of mTBI impact sit...
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Published in | Experimental brain research Vol. 235; no. 7; pp. 2133 - 2149 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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01.07.2017
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Abstract | Negative outcomes of mild traumatic brain injury (mTBI) can be exacerbated by repeated insult. Animal models of repeated closed-head mTBI provide the opportunity to define acute pathological mechanisms as the number of mTBI increases. Furthermore, little is known about the effects of mTBI impact site, and how this may affect brain function. We use a closed head, weight drop model of mTBI that allows head movement following impact, in adult female rats to determine the role of the number and location of mTBI on brain pathology and behaviour. Biomechanical assessment of two anatomically well-defined mTBI impact sites were used, anterior (bregma) and posterior (lambda). Location of the impact had no significant effect on impact forces (450 N), and the weight impact locations were on average 5.4 mm from the desired impact site. No between location vertical linear head kinematic differences were observed immediately following impact, however, in the 300 ms post-impact, significantly higher mean vertical head displacement and velocity were observed in the mTBI lambda trials. Breaches of the blood brain barrier were observed with three mTBI over bregma, associated with immunohistochemical indicators of damage. However, an increased incidence of hairline fractures of the skull and macroscopic haemorrhaging made bregma an unsuitable impact location to model repeated mTBI. Repeated mTBI over lambda did not cause skull fractures and were examined more comprehensively, with outcomes following one, two or three mTBI or sham, delivered at 1 day intervals, assessed on days 1–4. We observe a mild behavioural phenotype, with subtle deficits in cognitive function, associated with no identifiable neuroanatomical or inflammatory changes. However, an increase in lipid peroxidation in a subset of cortical neurons following two mTBI indicates increasing oxidative damage with repeated injury in female rats, supported by increased amyloid precursor protein immunoreactivity with three mTBI. This study of acute events following closed head mTBI identifies lipid peroxidation in neurons at the same time as cognitive deficits. Our study adds to existing literature, providing biomechanics data and demonstrating mild cognitive disturbances associated with diffuse injury, predominantly to grey matter, acutely following repeated mTBI. |
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AbstractList | Negative outcomes of mild traumatic brain injury (mTBI) can be exacerbated by repeated insult. Animal models of repeated closed-head mTBI provide the opportunity to define acute pathological mechanisms as the number of mTBI increases. Furthermore, little is known about the effects of mTBI impact site, and how this may affect brain function. We use a closed head, weight drop model of mTBI that allows head movement following impact, in adult female rats to determine the role of the number and location of mTBI on brain pathology and behaviour. Biomechanical assessment of two anatomically well-defined mTBI impact sites were used, anterior (bregma) and posterior (lambda). Location of the impact had no significant effect on impact forces (450 N), and the weight impact locations were on average 5.4 mm from the desired impact site. No between location vertical linear head kinematic differences were observed immediately following impact, however, in the 300 ms post-impact, significantly higher mean vertical head displacement and velocity were observed in the mTBI lambda trials. Breaches of the blood brain barrier were observed with three mTBI over bregma, associated with immunohistochemical indicators of damage. However, an increased incidence of hairline fractures of the skull and macroscopic haemorrhaging made bregma an unsuitable impact location to model repeated mTBI. Repeated mTBI over lambda did not cause skull fractures and were examined more comprehensively, with outcomes following one, two or three mTBI or sham, delivered at 1 day intervals, assessed on days 1-4. We observe a mild behavioural phenotype, with subtle deficits in cognitive function, associated with no identifiable neuroanatomical or inflammatory changes. However, an increase in lipid peroxidation in a subset of cortical neurons following two mTBI indicates increasing oxidative damage with repeated injury in female rats, supported by increased amyloid precursor protein immunoreactivity with three mTBI. This study of acute events following closed head mTBI identifies lipid peroxidation in neurons at the same time as cognitive deficits. Our study adds to existing literature, providing biomechanics data and demonstrating mild cognitive disturbances associated with diffuse injury, predominantly to grey matter, acutely following repeated mTBI. Negative outcomes of mild traumatic brain injury (mTBI) can be exacerbated by repeated insult. Animal models of repeated closed-head mTBI provide the opportunity to define acute pathological mechanisms as the number of mTBI increases. Furthermore, little is known about the effects of mTBI impact site, and how this may affect brain function. We use a closed head, weight drop model of mTBI that allows head movement following impact, in adult female rats to determine the role of the number and location of mTBI on brain pathology and behaviour. Biomechanical assessment of two anatomically well-defined mTBI impact sites were used, anterior (bregma) and posterior (lambda). Location of the impact had no significant effect on impact forces (450 N), and the weight impact locations were on average 5.4 mm from the desired impact site. No between location vertical linear head kinematic differences were observed immediately following impact, however, in the 300 ms post-impact, significantly higher mean vertical head displacement and velocity were observed in the mTBI lambda trials. Breaches of the blood brain barrier were observed with three mTBI over bregma, associated with immunohistochemical indicators of damage. However, an increased incidence of hairline fractures of the skull and macroscopic haemorrhaging made bregma an unsuitable impact location to model repeated mTBI. Repeated mTBI over lambda did not cause skull fractures and were examined more comprehensively, with outcomes following one, two or three mTBI or sham, delivered at 1 day intervals, assessed on days 1-4. We observe a mild behavioural phenotype, with subtle deficits in cognitive function, associated with no identifiable neuroanatomical or inflammatory changes. However, an increase in lipid peroxidation in a subset of cortical neurons following two mTBI indicates increasing oxidative damage with repeated injury in female rats, supported by increased amyloid precursor protein immunoreactivity with three mTBI. This study of acute events following closed head mTBI identifies lipid peroxidation in neurons at the same time as cognitive deficits. Our study adds to existing literature, providing biomechanics data and demonstrating mild cognitive disturbances associated with diffuse injury, predominantly to grey matter, acutely following repeated mTBI. |
Audience | Academic |
Author | Chin, Aaron Bartlett, Carole A. Alderson, Jacqueline Fehily, Brooke Yates, Nathanael J. Weir, Gillian Lydiard, Stephen Fitzgerald, Melinda |
Author_xml | – sequence: 1 givenname: Nathanael J. surname: Yates fullname: Yates, Nathanael J. organization: Experimental and Regenerative Neurosciences, School of Biological Sciences, The University of Western Australia – sequence: 2 givenname: Stephen surname: Lydiard fullname: Lydiard, Stephen organization: Experimental and Regenerative Neurosciences, School of Biological Sciences, The University of Western Australia – sequence: 3 givenname: Brooke surname: Fehily fullname: Fehily, Brooke organization: Experimental and Regenerative Neurosciences, School of Biological Sciences, The University of Western Australia – sequence: 4 givenname: Gillian surname: Weir fullname: Weir, Gillian organization: School of Sport Science, Exercise and Health, The University of Western Australia – sequence: 5 givenname: Aaron surname: Chin fullname: Chin, Aaron organization: School of Sport Science, Exercise and Health, The University of Western Australia – sequence: 6 givenname: Carole A. surname: Bartlett fullname: Bartlett, Carole A. organization: Experimental and Regenerative Neurosciences, School of Biological Sciences, The University of Western Australia – sequence: 7 givenname: Jacqueline surname: Alderson fullname: Alderson, Jacqueline organization: School of Sport Science, Exercise and Health, The University of Western Australia, Auckland University of Technology, Sports Performance Research Institute New Zealand (SPRINZ) – sequence: 8 givenname: Melinda orcidid: 0000-0002-4823-8179 surname: Fitzgerald fullname: Fitzgerald, Melinda email: lindy.fitzgerald@uwa.edu.au organization: Experimental and Regenerative Neurosciences, School of Biological Sciences, The University of Western Australia, Curtin Health Innovation Research Institute, Curtin University, Perron Institute for Nerurological and Translational Science, Sarich Neuroscience Research Institute |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28417146$$D View this record in MEDLINE/PubMed |
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Keywords | Oxidative stress Closed head Concussion Weight drop model Repeated mild traumatic brain injury Lipid peroxidation Female |
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SubjectTerms | Aldehydes - metabolism Alzheimer's disease Amyloid precursor protein Anatomy Animal models Animals Antigens - physiology Biomedical and Life Sciences Biomedicine Blood-brain barrier Blood-Brain Barrier - physiopathology Brain Brain - metabolism Brain - pathology Brain architecture Brain Injuries, Traumatic - complications Brain Injuries, Traumatic - pathology Brain research Calcium-Binding Proteins - metabolism Cell Death - physiology Cognition Disorders - etiology Cognitive ability Cohort Studies Disease Models, Animal Female Fractures Glial Fibrillary Acidic Protein - metabolism Head Head movement Health aspects Immunoreactivity Incidence Inflammation Injuries Lipid peroxidation Lipid Peroxidation - physiology Lipids Microfilament Proteins - metabolism Myelin Basic Protein - metabolism Neurologic Examination Neurology Neurons Neurons - metabolism Neurosciences Oligodendrocyte Transcription Factor 2 - metabolism Oxidative stress Oxidative Stress - physiology Pathology Physiological aspects Proteoglycans - physiology Rats Research Article Rodents Skull Substantia grisea Time Factors Traumatic brain injury Velocity β-Amyloid |
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Title | Repeated mild traumatic brain injury in female rats increases lipid peroxidation in neurons |
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