2007•Di-Si Junyi Daxue xuebaoRequires access

Effect of COX-2 protein expression on learning and memory function after severe traumatic brain injury in rats

Qing Liu

Open publisher page 0 citations

Abstract

AIM:To observe the expression of COX-2 and the effect of the selective COX-2 inhibitor NS-398 on learning and memory function of rats after traumatic brain injury(TBI).METHODS:The model of severe closed TBI was established according to the method created by Marmarou.Adult Wistar rats(n=360)were randomly divided into TBI group,NS-398 treatment group,and sham operation group,and each of them was sub-divided into post-traumatic 1,3,6,12,24,48,72,96,168 and 336 h groups.Another 120 rats were taken as normal controls.The NS-398 treatment group after injury was treated with NS-398 [40 mg/(kg·d)] ip.The TBI group,the sham operation group,and the control group were treated with normal saline.All rats were killed at each time point,for detecting COX-2 protein expression with Western Blot and immunohistochemistry.Another 24 rats were randomly divided into TBI group,NS-398 treatment group,sham operation group,and normal group.The cognitive dysfunction was evaluated using the Morris water maze(MWM).RESULTS:NS-398 could apparently down-regulate the peak of COX-2 protein expression in brain and obviously shorten the latency of Morris water maze tests.CONCLUSION:COX-2 is correlated with secondary brain injury induced by TBI,and NS-398 may effectively improve cognitive dysfunction after TBI.

About this research paper

What this paper is about

AIM:To observe the expression of COX-2 and the effect of the selective COX-2 inhibitor NS-398 on learning and memory function of rats after traumatic brain injury(TBI).METHODS:The model of severe closed TBI was established according to the method created by Marmarou.Adult Wistar rats(n=360)were randomly divided into TBI group,NS-398 treatment group,and sham operation group,and each of them was sub-divided into post-traumatic 1,3,6,12,24,48,72,96,168 and 336 h groups.Another 120 rats were taken as normal controls.The NS-398 treatment group after injury was treated with NS-398 [40 mg/(kg·d)] ip.The TBI group,the sham operation group,and the control group were treated with normal saline.All rats were killed at each time point,for detecting COX-2 protein expression with Western Blot and immunohistochemistry.Another 24 rats were randomly divided into TBI group,NS-398 treatment group,sham operation group,and normal group.The cognitive dysfunction was evaluated using the Morris water maze(MWM).RESULTS:NS-398 could apparently down-regulate the peak of COX-2 protein expression in brain and obviously shorten the latency of Morris water maze tests.CONCLUSION:COX-2 is correlated with secondary brain injury induced by TBI,and NS-398 may effectively improve cognitive dysfunction after TBI.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

AIM:To observe the expression of COX-2 and the effect of the selective COX-2 inhibitor NS-398 on learning and memory function of rats after traumatic brain injury(TBI).METHODS:The model of severe closed TBI was established according to the method created by Marmarou.Adult Wistar rats(n=360)were randomly divided into TBI group,NS-398 treatment group,and sham operation group,and each of them was sub-divided into post-traumatic 1,3,6,12,24,48,72,96,168 and 336 h groups.Another 120 rats were taken as normal controls.The NS-398 treatment group after injury was treated with NS-398 [40 mg/(kg·d)] ip.The TBI group,the sham operation group,and the control group were treated with normal saline.All rats were killed at each time point,for detecting COX-2 protein expression with Western Blot and immunohistochemistry.Another 24 rats were randomly divided into TBI group,NS-398 treatment group,sham operation group,and normal group.The cognitive dysfunction was evaluated using the Morris water maze(MWM).RESULTS:NS-398 could apparently down-regulate the peak of COX-2 protein expression in brain and obviously shorten the latency of Morris water maze tests.CONCLUSION:COX-2 is correlated with secondary brain injury induced by TBI,and NS-398 may effectively improve cognitive dysfunction after TBI.

Key concepts: Morris water navigation task, Traumatic brain injury, Medicine, Saline, Western blot, Immunohistochemistry, Hippocampus, Anesthesia

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of COX-2 protein expression on learning and memory function after severe traumatic brain injury in rats — Research Paper | ScholarLens