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Objective To study the effect of microgene pSVP oMcat implanted to modify schwann cell on growth associated protein -43(GAP -43)expression after spinal cord injury in adult rats.Method Hemisected of the T8segment of the sp inal cord was performed for all the experiment rats.The rats were randomly divided into three groups as follows:Group Awith microgene pSVPoMca t implanted to genetically modify SC;Group B with SC implanted ;Group C with hemisection of the spinal cord o nly.The changes of expression of GAP-43in spinal cord were observed by immunochemistry with antibodies against GAP -43.Simultaneous,the combined behavioral scores(CBS)was measured.Result There were not any different (P >0.05)among the three groups in first week a nd 12week.There were significant di ffeence(P <0.05)among three groups in 2nd,8th,and more dxpression of GAP -43at the 2nd week in gr oup A.The neurofunctional recovery was best in group A.Conclusion The microgene pSVPoMcat implanted t o modify schwann cell can promote the expression of GAP -43in spinal cord a nd func-tional recovery in adults rats after SCI.
Objective To study the effect of microgene pSVP oMcat implanted to modify schwann cell on growth associated protein -43 (GAP -43) expression after spinal cord injury in adult rats. Method Hemisected of the T8 segment of the sp inal cord was performed for all the experiment rats. The rats were randomly divided into three groups as follows: Group A with microgene pSVPoMca t implanted to genetically modify SC; Group B with SC implanted; Group C with hemisection of the spinal cord o nly. changes of expression of GAP-43in spinal cord were observed by immunochemistry with antibodies against GAP -43.Simultaneous, the combined behavioral scores (CBS) was measured. Result There were not any different (P> 0.05) among the three groups in first week a nd 12week.There were significant di ffeence (P <0.05) among three groups in 2nd, 8th, and more dxpression of GAP -43at the 2nd week in group A. The neurofunctional recovery was best in group A. Confluence The microgene pSVPoMcat implanted to modify schwann cell ca n promote the expression of GAP-43 in spinal cord a nd func-tional recovery in adult rats after SCI.