Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/23272
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Type: Journal article
Title: Soluble amyloid precursor protein a reduces neuronal injury and improves functional outcome following diffuse traumatic brain injury in rats
Author: Thornton, E.
Vink, R.
Blumbergs, P.
Van Den Heuvel, C.
Citation: Brain Research, 2006; 1094(1):38-46
Publisher: Elsevier Science Bv
Issue Date: 2006
ISSN: 0006-8993
1872-6240
Statement of
Responsibility: 
Emma Thornton, Robert Vink, Peter C. Blumbergs, and Corinna Van Den Heuvel
Abstract: Amyloid precursor protein (APP) has previously been shown to increase following traumatic brain injury (TBI). Whereas a number of investigators assume that increased APP may lead to the production of neurotoxic Abeta and be deleterious to outcome, the soluble alpha form of APP (sAPPalpha) is a product of the non-amyloidogenic cleavage of amyloid precursor protein that has previously been shown in vitro to have many neuroprotective and neurotrophic functions. However, no study to date has addressed whether sAPPalpha may be neuroprotective in vivo. The present study examined the effects of in vivo, posttraumatic sAPPalpha administration on functional motor outcome, cellular apoptosis, and axonal injury following severe impact-acceleration TBI in rats. Intracerebroventricular administration of sAPPalpha at 30 min posttrauma significantly improved motor outcome compared to vehicle-treated controls as assessed using the rotarod task. Immunohistochemical analysis using antibodies directed toward caspase-3 showed that posttraumatic treatment with sAPPalpha significantly reduced the number of apoptotic neuronal perikarya within the hippocampal CA3 region and within the cortex 3 days after injury compared to vehicle-treated animals. Similarly, sAPPalpha-treated animals demonstrated a reduction in axonal injury within the corpus callosum at all time points, with the reduction being significant at both 3 and 7 days postinjury. Our results demonstrate that in vivo administration of sAPPalpha improves functional outcome and reduces neuronal cell loss and axonal injury following severe diffuse TBI in rats. Promotion of APP processing toward sAPPalpha may thus be a novel therapeutic strategy in the treatment of TBI.
Keywords: Axonal injury
Caspase-3
Immunohistochemistry
Rat
Soluble amyloid precursor protein α
Traumatic brain injury
Description: Copyright © 2006 Elsevier B.V. All rights reserved.
DOI: 10.1016/j.brainres.2006.03.107
Description (link): http://www.elsevier.com/wps/find/journaldescription.cws_home/506048/description#description
Appears in Collections:Aurora harvest 6
Paediatrics publications

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