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https://hdl.handle.net/2440/38762
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dc.contributor.author | Cernak, I. | - |
dc.contributor.author | O'Connor, C. | - |
dc.contributor.author | Vink, R. | - |
dc.date.issued | 2001 | - |
dc.identifier.citation | Clinical and Experimental Pharmacology and Physiology, 2001; 28(11):922-925 | - |
dc.identifier.issn | 0305-1870 | - |
dc.identifier.issn | 1440-1681 | - |
dc.identifier.uri | http://hdl.handle.net/2440/38762 | - |
dc.description | The definitive version is available at www.blackwell-synergy.com Article first published online: 12 JAN 2002 | - |
dc.description.abstract | 1. Post-traumatic inflammation may play a significant role in the development of delayed secondary brain damage following traumatic brain injury. 2. During post-traumatic inflammation, metabolic products of arachidonic acid, known as prostanoids (prostaglandins and thromboxanes) are released and aggravate the injury process. Prostanoid synthesis is regulated by the enzyme cyclo-oxygenase (COX), which is present in at least two isoforms, COX-1 (the constitutive form) and COX-2 (the inducible form). 3. In the present study, we examine the temporal and spatial profiles of COX-2 expression and the effects of the COX-2 inhibitor nimesulide on motor and cognitive outcome following diffuse traumatic brain injury in rats. 4. Adult male Sprague-Dawley rats were injured using the 2 m impact acceleration model of diffuse traumatic brain injury. At preselected time points after injury, animals were killed and the expression of COX-2 was measured in the cortex and hippocampus by western blotting techniques. 5. Increased expression of COX-2 was found in the cortex at 3 days and in the hippocampus as early as 3 h postinjury and this persisted for at least 12 days. 6. Administration of nimesulide (6 mg/kg, i.p.) at 30 min after injury and daily over a 10 day post-traumatic neurological assessment period resulted in a significant improvement compared with vehicle (2% dimethylsulphoxide diluted in isotonic saline)-treated controls in cognitive deficits, as assessed by the Barnes circular maze. There was also a significant improvement in motor dysfunction as assessed by the rotarod test on days 1 and 2 post-trauma compared with vehicle-treated controls. 7. These results implicate the involvement of COX-2 in cognitive and motor dysfunction following diffuse traumatic brain injury. | - |
dc.description.statementofresponsibility | I Cernak, C O'Connor, R Vink | - |
dc.language.iso | en | - |
dc.publisher | Blackwell Publishing Asia | - |
dc.rights | Copyright © 2001 John Wiley & Sons, Inc. All Rights Reserved. | - |
dc.source.uri | http://dx.doi.org/10.1046/j.1440-1681.2001.03549.x | - |
dc.subject | diffuse axonal injury | - |
dc.subject | neurological outcome | - |
dc.subject | neurotrauma | - |
dc.subject | nimesulide | - |
dc.title | Activation of cyclo-oxygenase-2 contributes to motor and cognitive dysfunction following diffuse traumatic brain injury in rats | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1046/j.1440-1681.2001.03549 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Vink, R. [0000-0002-4885-0667] | - |
Appears in Collections: | Anatomical Sciences publications Aurora harvest 6 |
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