Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol

<p>Abstract</p> <p>Polyethylene glycol (PEG; 2000 MW, 30% by volume) has been shown to mechanically repair damaged cellular membranes and reduce secondary axotomy after traumatic brain and spinal cord injury (TBI and SCI respectively). This repair is achieved following spontaneous...

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Main Authors: Borgens Richard B, Colby Julia M, Koob Andrew O
Format: Article
Language:English
Published: BMC 2008-06-01
Series:Journal of Biological Engineering
Online Access:http://www.jbioleng.org/content/2/1/9
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spelling doaj-c97456b753644c53afaee6f5a00238622020-11-24T21:52:51ZengBMCJournal of Biological Engineering1754-16112008-06-0121910.1186/1754-1611-2-9Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycolBorgens Richard BColby Julia MKoob Andrew O<p>Abstract</p> <p>Polyethylene glycol (PEG; 2000 MW, 30% by volume) has been shown to mechanically repair damaged cellular membranes and reduce secondary axotomy after traumatic brain and spinal cord injury (TBI and SCI respectively). This repair is achieved following spontaneous reassembly of cell membranes made possible by the action of targeted hydrophilic polymers which first seal the compromised portion of the plasmalemma, and secondarily, allow the lipidic core of the compromised membranes to resolve into each other. Here we compared PEG-treated to untreated rats using a computer-managed open-field behavioral test subsequent to a standardized brain injury. Animals were evaluated after a 2-, 4-, and 6-hour delay in treatment after TBI. Treated animals receive a single subcutaneous injection of PEG. When treated within 2 hours of the injury, injured PEG-treated rats showed statistically significant improvement in their exploratory behavior recorded in the activity box when compared to untreated but brain-injured controls. A delay of 4 hours reduced this level of achievement, but a statistically significant improvement due to PEG injection was still clearly evident in most outcome measures compared at the various evaluation times. A further delay of 2 more hours, however, eradicated the beneficial effects of PEG injection as revealed using this behavioral assessment. Thus, there appears to be a critical window of time in which PEG administration after TBI can provide neuroprotection resulting in an enhanced functional recovery. As is often seen in clinically applied acute treatments for trauma, the earlier the intervention can be applied, the better the outcome.</p> http://www.jbioleng.org/content/2/1/9
collection DOAJ
language English
format Article
sources DOAJ
author Borgens Richard B
Colby Julia M
Koob Andrew O
spellingShingle Borgens Richard B
Colby Julia M
Koob Andrew O
Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
Journal of Biological Engineering
author_facet Borgens Richard B
Colby Julia M
Koob Andrew O
author_sort Borgens Richard B
title Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
title_short Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
title_full Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
title_fullStr Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
title_full_unstemmed Behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
title_sort behavioral recovery from traumatic brain injury after membrane reconstruction using polyethylene glycol
publisher BMC
series Journal of Biological Engineering
issn 1754-1611
publishDate 2008-06-01
description <p>Abstract</p> <p>Polyethylene glycol (PEG; 2000 MW, 30% by volume) has been shown to mechanically repair damaged cellular membranes and reduce secondary axotomy after traumatic brain and spinal cord injury (TBI and SCI respectively). This repair is achieved following spontaneous reassembly of cell membranes made possible by the action of targeted hydrophilic polymers which first seal the compromised portion of the plasmalemma, and secondarily, allow the lipidic core of the compromised membranes to resolve into each other. Here we compared PEG-treated to untreated rats using a computer-managed open-field behavioral test subsequent to a standardized brain injury. Animals were evaluated after a 2-, 4-, and 6-hour delay in treatment after TBI. Treated animals receive a single subcutaneous injection of PEG. When treated within 2 hours of the injury, injured PEG-treated rats showed statistically significant improvement in their exploratory behavior recorded in the activity box when compared to untreated but brain-injured controls. A delay of 4 hours reduced this level of achievement, but a statistically significant improvement due to PEG injection was still clearly evident in most outcome measures compared at the various evaluation times. A further delay of 2 more hours, however, eradicated the beneficial effects of PEG injection as revealed using this behavioral assessment. Thus, there appears to be a critical window of time in which PEG administration after TBI can provide neuroprotection resulting in an enhanced functional recovery. As is often seen in clinically applied acute treatments for trauma, the earlier the intervention can be applied, the better the outcome.</p>
url http://www.jbioleng.org/content/2/1/9
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