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机构地区:[1]莆田学院医学院人体解剖与组织胚胎学教研室,莆田351100 [2]福建医科大学人体解剖学与组织胚胎学系,福州350001
出 处:《解剖学杂志》2007年第5期582-584,601,共4页Chinese Journal of Anatomy
基 金:福建省教育厅科技项目(JA05322)
摘 要:目的:探讨硫酸软骨素酶ABC对严重的大鼠脊髓损伤蛋白多糖及生长相关蛋白43(GAP-43)基因表达的影响。方法:制作大鼠脊髓横断伤模型,分为脊髓损伤组和脊髓损伤治疗组,给于治疗组硫酸软骨素酶ABC鞘内注射,用免疫荧光组织化学观察硫酸软骨素蛋白多糖(CSPGs)的表达,半定量RT-PCR、Western印迹法观察GAP-43 mR- NA及蛋白的表达。结果:治疗组与损伤组比较,CSPGs的表达减少,差异具有显著性,而GAP-43mRNA及蛋白表达增多。结论:硫酸软骨素酶ABC能够裂解CSPGs,改善脊髓损伤区的微环境,促进GAP-43 mRNA及蛋白的表达,是修复脊髓损伤和促进神经再生的机制之一。Objective: To investigate the effects of chondroitinase ABC on chondroitin sulfate proteoglycans (CSPGs) and growth associated protein-43 (GAP-43) after spinal cord injury in rats. Methods: The model of rat spinal cord transection was made and divided into spinal cord injury group (Group A) and treatment group (Group B), which was injected with 20/A chondroitinase ABC (0.2 units/ml). Immunofluorescent histochemical staining was used to observe the dissolving effect of chondroitin sulfate proteoglycans; Then GAP-43 was tested by semiquantitative RT-PCR and Western-blot. Results: The fluorescence intensity of CSPGs of Group B was significantly less than that of group A (P〈0. 05). Contrarily the expressions of GAP-43 mRNA and protein in Group B were higher than those in Group A (P〈0. 05). Conclusion: Chondroitinase ABC might split CSPGs, improve microenvironment of the injured region,and enhance the expression of GAP-43, which is one of the mechanism of repairing the spinal cord injury.
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