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妊娠期糖尿病会影响大鼠后代的视网膜穆勒细胞。

Gestational diabetes influences retinal Muller cells in rat's offspring.

作者信息

Tabasi Akramsadat, Ghafari Soraya, Mehdizadeh Mehdi, Shekari Majid Asadi, Golalipour Mohammad Jafar

机构信息

Department of Anatomical Sciences, Golestan University of Medical Sciences, Gorgan, Iran.

Gorgan Congenital Malformations Research Center, Department of Anatomical Sciences, Golestan University of Medical Sciences, Gorgan, Iran.

出版信息

Iran J Basic Med Sci. 2017 Feb;20(2):216-221. doi: 10.22038/ijbms.2017.8251.

Abstract

OBJECTIVES

The Muller cell is the principal glial cell of the vertebrate retina. The expression of Glial fibrillary acidic protein (GFAP) in the Muller cells was used as a cellular marker for retinal damage. This study was done to evaluate the effect of gestational diabetes on retinal Muller cells in rat's offspring.

MATERIALS AND METHODS

In this experimental study, 12 Wistar rat dams were randomly allocated in control and diabetic groups. Gestational diabetes was induced by 40 mg/kg/body weight of streptozotocin at the first day of gestation, intraperitoneally. Dams in control group received an equivalent volume normal saline. Eye of six offspring of each group were removed at postnatal day 28 (P28). The histopathological changes in retina were examined through H&E staining and ultrastructure transmission electron microscopy (TEM). The expression of GFAP was examined using Immunohisto-chemical staining of GFAP in Muller cells. Photographs of retina were taken using Olympus BX51 microscope and a digital camera DP12 and EM LEO906; Zeiss, Germany.

RESULTS

In the control rat's offspring, GFAP expression was not significant in Muller cells. According to the optical microscope images, GFAP expression was observed in the processes of the Muller cell in the inner plexiform layer of retina in offspring of diabetic mothers. In TEM technique, nuclear fragmentation and apoptotic bodies were observed in Muller cell of diabetic offspring.

CONCLUSION

This study showed that the uncontrolled gestational diabetes can increase GFAP expression in Muller cells and retinal thickness of retinal layer in rat offspring's, therefore uncontrolled gestational can damage the Muller cells.

摘要

目的

穆勒细胞是脊椎动物视网膜的主要神经胶质细胞。穆勒细胞中胶质纤维酸性蛋白(GFAP)的表达被用作视网膜损伤的细胞标志物。本研究旨在评估妊娠期糖尿病对大鼠后代视网膜穆勒细胞的影响。

材料与方法

在本实验研究中,将12只Wistar大鼠母鼠随机分为对照组和糖尿病组。在妊娠第一天腹腔注射40mg/kg体重的链脲佐菌素诱导妊娠期糖尿病。对照组母鼠注射等量生理盐水。在出生后第28天(P28)取每组6只后代的眼睛。通过苏木精-伊红(H&E)染色和超微结构透射电子显微镜(TEM)检查视网膜的组织病理学变化。使用穆勒细胞中GFAP的免疫组织化学染色检查GFAP的表达。使用奥林巴斯BX51显微镜和数码相机DP12以及EM LEO906(德国蔡司)拍摄视网膜照片。

结果

在对照大鼠的后代中,穆勒细胞中GFAP表达不显著。根据光学显微镜图像,在糖尿病母亲后代的视网膜内网状层的穆勒细胞的突起中观察到GFAP表达。在TEM技术中,在糖尿病后代的穆勒细胞中观察到核碎裂和凋亡小体。

结论

本研究表明,未控制的妊娠期糖尿病可增加大鼠后代穆勒细胞中GFAP的表达和视网膜层的视网膜厚度,因此未控制的妊娠期糖尿病可损害穆勒细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c81/5339664/fd338eddff75/IJBMS-20-216-g001.jpg

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