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Early adaptive response of the retina to a pro-diabetogenic diet: Impairment of cone response and gene expression changes in high-fructose fed rats

机译:视网膜对促糖尿病饮食的早期适应性反应:高果糖喂养大鼠视锥反应和基因表达变化的损害

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摘要

The lack of plasticity of neurons to respond to dietary changes, such as high fat and high fructose diets, by modulating gene and protein expression has been associated with functional and behavioral impairments that can have detrimental consequences. The inhibition of high fat-induced rewiring of hypothalamic neurons induced obesity. Feeding rodents with high fructose is a recognized and widely used model to trigger obesity and metabolic syndrome. However the adaptive response of the retina to short term feeding with high fructose is poorly documented. We therefore aimed to characterize both the functional and gene expression changes in the neurosensory retina of Brown Norway rats fed during 3 and 8 days with a 60%-rich fructose diet (n = 16 per diet and per time point). Glucose, insulin, leptin, triacylglycerols, total cholesterol, HDL-cholesterol, LDL-cholesterol and fructosamine were quantified in plasma (n = 8 in each group). Functionality of the inner retina was studied using scotopic single flash electroretinography (n = 8 in each group) and the individual response of rod and cone photoreceptors was determined using 8.02 Hz Flicker electroretinography (n = 8 in each group). Analysis of gene expression in the neurosensory retina was performed by Affymetrix genechips, and confirmed by RT-qPCR (n = 6 in each group). Elevated glycemia (+13%), insulinemia (+83%), and leptinemia (+172%) was observed after 8 days of fructose feeding. The cone photoreceptor response was altered at day 8 in high fructose fed rats (A = 0.5 log unit of light stimulus intensity). Affymetrix analysis of gene expression highlighted significant modulation of the pathimays of eIF2 signaling and endoplasmic reticulum stress, regulation of eIF4 and p70S6K signaling, as well as mTOR signaling and mitochondrial dysfunction. RT-qPCR analysis confirmed the down regulation of Crystallins, Npy, Nid1 and Optc genes after 3 days of fructose feeding, and up regulation of End2. Meanwhile, a trend towards an increased expression of alpha A- and alpha B-clystallin proteins was observed at day 8. Our results are consistent with early alterations of the functioning and gene expression in the retina in a pro diabetogenic environment. (C) 2015 Elsevier Ltd. All rights reserved.
机译:神经元缺乏通过调节基因和蛋白质表达来响应饮食变化(例如高脂肪和高果糖饮食)的可塑性,与功能和行为受损有关,可能造成不利后果。抑制高脂肪诱导的下丘脑神经元重新布线可导致肥胖。用高果糖喂养啮齿动物是引发肥胖和代谢综合症的公认且广泛使用的模型。但是,很少有人记录视网膜对高果糖短期喂养的适应性反应。因此,我们旨在表征在富含果糖含量为60%的布朗挪威大鼠于3天和8天的神经感觉视网膜中功能和基因表达的变化(n =每个饮食和每个时间点16个)。在血浆中定量葡萄糖,胰岛素,瘦素,三酰基甘油,总胆固醇,HDL-胆固醇,LDL-胆固醇和果糖胺(每组n = 8)。使用暗视单闪视网膜电图(每组n = 8)研究了内部视网膜的功能,并使用8.02 Hz闪烁电视网膜电图(每组n = 8)确定了视杆和视锥感光器的个体反应。通过Affymetrix基因芯片对神经感觉视网膜中的基因表达进行分析,并通过RT-qPCR进行确认(每组n = 6)。果糖喂养8天后,血糖升高(+ 13%),胰岛素血症(+ 83%)和瘦素血症(+ 172%)。高果糖喂养的大鼠(A = 0.5 log单位的光刺激强度)在第8天,锥体感光细胞反应发生改变。 Affymetrix对基因表达的分析突显了对eIF2信号和内质网应激病的显着调节,对eIF4和p70S6K信号的调控以及mTOR信号和线粒体功能障碍。 RT-qPCR分析证实果糖喂养3天后,Crystallins,Npy,Nid1和Optc基因下调,而End2上调。同时,在第8天观察到了αA和αB Clystallin蛋白表达增加的趋势。我们的结果与在促糖尿病环境中视网膜功能和基因表达的早期改变是一致的。 (C)2015 Elsevier Ltd.保留所有权利。

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