Elucidating opportunities and pitfalls in the treatment of experimental traumatic brain injury to optimize and facilitate clinical translation
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Final Accepted Manuscript
Author
de la Tremblaye, Patricia B.O’Neil, Darik A.
LaPorte, Megan J.
Cheng, Jeffrey P.
Beitchman, Joshua A.
Thomas, Theresa Currier
Bondi, Corina O.
Kline, Anthony E.
Affiliation
Univ Arizona, Coll Med, Dept Child HlthIssue Date
2018-02Keywords
Antiepileptic drugs (AEDs)Antipsychotic drugs (APDs)
Controlled cortical impact (CCI)
Endocannabinoids
Executive function
Fluid percussion (FP) injury
Morris water maze (MWM)
Rehabilitation
Stress
Traumatic brain injury (TBI)
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PERGAMON-ELSEVIER SCIENCE LTDCitation
Patricia, B., O’Neil, D. A., LaPorte, M. J., Cheng, J. P., Beitchman, J. A., Thomas, T. C., ... & Kline, A. E. (2017). Elucidating opportunities and pitfalls in the treatment of experimental traumatic brain injury to optimize and facilitate clinical translation. Neuroscience & Biobehavioral Reviews.Rights
© 2017 Elsevier Ltd. All rights reserved.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
The aim of this review is to discuss the research presented in a symposium entitled "Current Progress in characterizing therapeutic strategies and challenges in experimental CNS injury" which was presented at the 2016 International Behavioral Neuroscience Society annual meeting. Herein we discuss diffuse and focal traumatic brain injury (TBI) and ensuing chronic behavioral deficits as well as potential rehabilitative approaches. We also discuss the effects of stress on executive function after TBI as well as the response of the endocrine system and regulatory feedback mechanisms. The role of the endocannabinoids after CNS injury is also discussed. Finally, we conclude with a discussion of antipsychotic and antiepileptic drugs, which are provided to control TBI-induced agitation and seizures, respectively. The review consists predominantly of published data.Note
18 month embargo; published online: 30 May 2017ISSN
01497634PubMed ID
28576511Version
Final accepted manuscriptSponsors
National Institutes of Health [HD069620, HD069620-S1, NS060005, NS084967, NS094950, NS099683]; University of Pittsburgh Physicians/UPMC Academic Foundation; Arizona Biomedical Research Commission through Arizona Department of Health Services [ADHS14-00003606]; Valley Research Partnership Awards [P2201607, P1201607]; Phoenix Children's Hospital Mission Support FundsAdditional Links
http://linkinghub.elsevier.com/retrieve/pii/S014976341730088Xae974a485f413a2113503eed53cd6c53
10.1016/j.neubiorev.2017.05.022
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