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详细评估 Zucker 糖尿病肥胖(ZDF)大鼠视网膜中可能的神经节细胞损失。

Detailed Evaluation of Possible Ganglion Cell Loss in the Retina of Zucker Diabetic Fatty (ZDF) Rats.

机构信息

Department of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.

Department of Ophthalmology, Semmelweis University, Budapest, Hungary.

出版信息

Sci Rep. 2019 Jul 18;9(1):10463. doi: 10.1038/s41598-019-46879-1.

DOI:10.1038/s41598-019-46879-1
PMID:31320684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6639371/
Abstract

A thinning of the inner retina is one of the earliest potential markers of neuroretinal damage in diabetic subjects. The histological background is uncertain; retinal ganglion cell (RGC) loss and changes in the structure or thickness of the inner plexiform layer (IPL) have been suspected. Studies conducted on animal models on RGC pathology gave contradictory results. Hereby we present RGC numbers, distribution patterns and IPL thickness from Zucker Diabetic Fatty (ZDF) rats. After labelling RGCs on retinal whole mounts, isodensity maps were constructed, RGC numbers and distribution patterns analysed using a custom-built algorithm, enabling point-by-point comparison. There was no change in staining characteristics of the antibodies and no significant difference in average RGC densities was found compared to controls. The distribution patterns were also comparable and no significant difference was found in IPL thickness and stratification or in the number of apoptotic cells in the ganglion cell layer (GCL). Our results provide a detailed evaluation of the inner retina and exclude major RGC loss in ZDF rats and suggest that other factors could serve as a potential explanation for inner retinal thinning in clinical studies. Our custom-built method could be adopted for the assessment of other animal or human retinas.

摘要

内视网膜变薄是糖尿病患者神经视网膜损伤的早期潜在标志物之一。其组织学背景尚不确定;怀疑视网膜神经节细胞 (RGC) 丢失以及内丛状层 (IPL) 的结构或厚度发生变化。对动物模型中 RGC 病理学的研究得出了相互矛盾的结果。在此,我们展示了 Zucker 糖尿病肥胖 (ZDF) 大鼠的 RGC 数量、分布模式和 IPL 厚度。在对视网膜全层进行 RGC 标记后,构建等密度图,使用定制的算法分析 RGC 数量和分布模式,实现逐点比较。抗体的染色特征没有变化,与对照组相比,平均 RGC 密度也没有显著差异。分布模式也相似,IPL 厚度和分层以及节细胞层 (GCL) 中凋亡细胞的数量也没有显著差异。我们的结果对内视网膜进行了详细评估,排除了 ZDF 大鼠中主要的 RGC 丢失,并表明在临床研究中其他因素可能是内视网膜变薄的潜在解释。我们定制的方法可用于评估其他动物或人类的视网膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/fb92a6ce3d8f/41598_2019_46879_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/3a4460346049/41598_2019_46879_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/703b8ca3ad9c/41598_2019_46879_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/90d7baa5ee3d/41598_2019_46879_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/ef746eaec097/41598_2019_46879_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/e1ee4674d6a6/41598_2019_46879_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/f1a92e1eed7f/41598_2019_46879_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/70707512bda5/41598_2019_46879_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/fb92a6ce3d8f/41598_2019_46879_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/3a4460346049/41598_2019_46879_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/703b8ca3ad9c/41598_2019_46879_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/90d7baa5ee3d/41598_2019_46879_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/ef746eaec097/41598_2019_46879_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/e1ee4674d6a6/41598_2019_46879_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/f1a92e1eed7f/41598_2019_46879_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/70707512bda5/41598_2019_46879_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6097/6639371/fb92a6ce3d8f/41598_2019_46879_Fig8_HTML.jpg

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