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pigment epithelium-derived factor protects the morphological structure of retinal Müller cells in diabetic rats

pigment epithelium-derived factor protects the morphological structure of retinal Müller cells in diabetic rats

作     者:Xiao-Hui Zhang Zhao-Hui Feng Yi Zhang 

作者机构:Department of Ophthalmologythe Second Affiliated Hospital of Xi'an Jiaotong University Medical College 

出 版 物:《International Journal of Ophthalmology(English edition)》 (国际眼科杂志(英文版))

年 卷 期:2014年第7卷第6期

页      面:941-946页

核心收录:

学科分类:1002[医学-临床医学] 100212[医学-眼科学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学] 

基  金:Supported by Shaanxi Province Science and Technology Research and Development Program (No. 2012K16-06-05) 

主  题:diabetes mellitus pigment epitheliumderived factor retinal Müller cells glutamine synthase glial fibrillary acidic protein 

摘      要:AIM: To investigate if pigment epithelium-derived factor(PEDF) has any protective effect on the retinal Müller cells of Sprague-Dawley rats suffering from diabetes ***: Sixty Sprague-Dawley rats were randomly divided into a negative control group, a group receiving0.1 μg/μL PEDF, another group receiving 0.2 μg/μL PEDF,and a group receiving balanced salt solution(BSS). Rats in both the PEDF and BSS groups were treated intravitreally based on previously established diabetic models. After 4wk of treatment, morphological alterations of Müller cells and protein expression of glutamine synthase(GS) and glial fibrillary acidic protein(GFAP)were ***:PEDFateither0.1μg/μLor0.2μg/μLsignificantly improved the structures of both nuclei and organelles of Müller cells compared to the BSS-treated *** of GS was significantly higher in the 0.2 μg/μL PEDF group than that in the BSS group(P =0.012), but expression of GFAP was significantly lower in the 0.2 μg/μL PEDF group than that in the BSS group(P =0.000);however, there were no significant differences in expression of these proteins between the 0.1 μg/μL PEDF group and the BSS group(P =0.608, P =0.152). CONCLUSION: PEDF protects the morphological ultrastructure of Müller cells, improves the expression of glutamate synthase and prevents cell gliosis.

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