辛伐他汀对高脂饮食致小鼠视网膜病变保护作用的组织学研究

F. Ahmad, Rania A. Zidan
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引用次数: 1

摘要

背景:高脂饲料饲喂是研究胰岛素抵抗、2型糖尿病和肥胖(包括视网膜病变)引起的变化的重要模型。血管内皮生长因子(VEGF)和p53与视网膜病变的发展有关。目的:他的研究目的是分析高脂肪动脉粥样硬化小鼠模型的视网膜组织学变化,并评估辛伐他汀对这些变化的可能保护作用,包括对VEGF和p53表达的影响。材料与方法:选取6周龄小鼠27只,根据小鼠的饮食和给药情况分为3组;第一组是正常均衡饮食喂养的小鼠,第二组是hfd喂养的小鼠,第三组是hfd喂养的小鼠,每天服用辛伐他汀,持续30周。所有小鼠随访30周。在36周龄的研究结束时,收集眼部组织并使用光学显微镜检查视网膜切片。比较三组视网膜各层厚度。采用免疫组化分析确定VEGF在视网膜中的定位,采用p53评估凋亡细胞死亡。结果:饲喂hfd的小鼠视网膜厚度增加,外核层细胞间隙扩大。许多内核层细胞出现细胞质空泡。VEGF在视网膜神经节细胞层和核细胞层的表达明显升高。内视网膜内p53反应升高。辛伐他汀治疗组的组织学改变明显改善。结论:hfd诱导视网膜层结构改变,同时VEGF和p53表达上调。辛伐他汀可改善这些视网膜病变。
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Histological Study on the Protective Effect of Simvastatin on the Retinal Changes Induced by High-Fat Diet in Mice -
Background: High-fat diet (HFD) feeding is an important model to study the changes induced by insulin resistance, Type 2 diabetes mellitus and obesity including retinopathy. Vascular endothelial growth factor (VEGF) and p53 have been implicated in the development of retinopathy. Objectives: The aim of his study was to analyze histological retinal changes in a high-fat atherogenic mouse model and to evaluate the possible protective effect of simvastatin on these changes including its effects on the expression of VEGF and p53. Materials and Methods: A total of 27 mice (6 weeks old) were divided into 3 study groups according to their diet and treatment given; Group I - normal balanced diet-fed mice, Group II - HFD-fed mice, and Group III - HFD-fed mice treated with simvastatin daily for 30 weeks. All mice were followed up for 30 weeks. At the end of the study at 36 weeks of age, eye tissues were collected and retinal sections were examined using light microscopy. Comparison of the thickness of retinal layers in the three groups was carried out. The localization of VEGF in the retina was determined by immunohistochemical analysis, and apoptotic cell death was assessed using the p53. Results: In the HFD-fed mice, there was an increase in the retinal thickness associated with presence of wide intercellular spaces in the outer nuclear layer. Many cells in the inner nuclear layer showed cytoplasmic vacuolations. Expression of VEGF was significantly increased in the retinal ganglion cell layers and nuclear cell layers. Elevated p53 reaction was demonstrated within the inner retina. The histological changes were significantly improved in the simvastatin treated group. Conclusions: HFD-induced structural changes in the retinal layers and simultaneous upregulation of VEGF and p53. Administration of simvastatin improved these retinal alterations.
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