摘要
目的:探讨过量谷氨酸毒性损伤后视网膜天冬氨酸蛋白酶-3(Caspase-3)和凋亡相关蛋白Bcl-2的表达及碱性成纤维细胞生长因子(bFGF)对兴奋毒性损伤的保护作用.方法: 豚鼠随机分为正常对照组、谷氨酸损伤组、bFGF治疗组.采用免疫组织化学方法和图像分析技术,对各组豚鼠视网膜内Caspase-3和Bcl-2的表达进行检测.结果: 对照组Caspase-3无明显表达,损伤组在节细胞层、内核层、内界膜和外界膜等处Caspase-3表达阳性面积百分率和密度明显上调,bFGF治疗组Caspase-3表达明显降低.对照组Bcl-2在节细胞层、神经纤维层及内核层内有弱阳性表达,损伤后变化不明显,bFGF治疗组Bcl-2的表达阳性面积百分率和密度明显上调,不仅在节细胞层、内核层和外界膜,在内界膜、外网状层、外核层也有明显表达.结论: bFGF能选择性减少视网膜兴奋毒性损伤后Caspase-3的表达,增加Bcl-2的表达,bFGF抗过量谷氨酸诱导的节细胞凋亡的机制之一可能是调节Mǘller细胞及节细胞内Caspase-3和Bcl-2的表达.
Objective: To assess the expression of Bcl-2 and Caspase-3 in the retina after superabundant glutamate injury and investigate the neural protective effect of basic fibroblast growth factor (bFGF) on retinal excitotoxicity damage in guinea pigs. Methods: Guinea pigs were randomly divided into a glutamate injury model group, a normal control group and a bFGF treatment group. The expression of Bcl-2 and Caspase-3 in the retina was detected by immunohistochemical method and image analysis. Results: A few of Caspase-3 positive cells were found in the normal control group; the expression of Caspase-3 was significantly increased in the injury group; and Bcl-2 showed weak expression in the retina of the normal control group and there was no significant change after damage. The expression of Bcl-2 significantly increased and the expression of Caspase-3 reduced in the treatment group received bFGF injection beforehand. There was significant difference between the treatment group and model group. Conclusion: bFGF might selectively reduce the expression of Caspase-3 and up-regulate the expression of Bcl-2 in the retina after supera- bundant glutamate injury, and one of the possible mechanisms is the inhibition of glutamate-injured RGCs apoptosis by bFGF.
出处
《解剖学杂志》
CAS
CSCD
北大核心
2011年第1期70-72,113,共4页
Chinese Journal of Anatomy