Obesogenic Diets Cause Alterations on Proteins and Theirs Post-Translational Modifications in Mouse Brains.

IF 2.3 Q3 NUTRITION & DIETETICS Nutrition and Metabolic Insights Pub Date : 2021-05-03 eCollection Date: 2021-01-01 DOI:10.1177/11786388211012405
Valentina Siino, Pia Jensen, Peter James, Sonya Vasto, Antonella Amato, Flavia Mulè, Giulia Accardi, Martin Røssel Larsen
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引用次数: 4

Abstract

Obesity constitutes a major global health threat and is associated with a variety of diseases ranging from metabolic and cardiovascular disease, cancer to neurodegeneration. The hallmarks of neurodegeneration include oxidative stress, proteasome impairment, mitochondrial dysfunction and accumulation of abnormal protein aggregates as well as metabolic alterations. As an example, in post-mortem brain of patients with Alzheimer's disease (AD), several studies have reported reduction of insulin, insulin-like growth factor 1 and insulin receptor and an increase in tau protein and glycogen-synthase kinase-3β compared to healthy controls suggesting an impairment of metabolism in the AD patient's brain. Given these lines of evidence, in the present study we investigated brains of mice treated with 2 obesogenic diets, high-fat diet (HFD) and high-glycaemic diet (HGD), compared to mice fed with a standard diet (SD) employing a quantitative mass spectrometry-based approach. Moreover, post-translational modified proteins (phosphorylated and N-linked glycosylated) were studied. The aim of the study was to identify proteins present in the brain that are changing their expression based on the diet given to the mice. We believed that some of these changes would highlight pathways and molecular mechanisms that could link obesity to brain impairment. The results showed in this study suggest that, together with cytoskeletal proteins, mitochondria and metabolic proteins are changing their post-translational status in brains of obese mice. Specifically, proteins involved in metabolic pathways and in mitochondrial functions are mainly downregulated in mice fed with obesogenic diets compared to SD. These changes suggest a reduced metabolism and a lower activity of mitochondria in obese mice. Some of these proteins, such as PGM1 and MCT1 have been shown to be involved in brain impairment as well. These results might shed light on the well-studied correlation between obesity and brain damage. The results presented here are in agreement with previous findings and aim to open new perspectives on the connection between diet-induced obesity and brain impairment.

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致肥性饮食导致小鼠大脑中蛋白质及其翻译后修饰的改变。
肥胖是一个主要的全球健康威胁,与从代谢和心血管疾病、癌症到神经退行性疾病等多种疾病有关。神经变性的特征包括氧化应激、蛋白酶体损伤、线粒体功能障碍、异常蛋白聚集体的积累以及代谢改变。例如,在阿尔茨海默病(AD)患者死后的大脑中,一些研究报告了与健康对照相比,胰岛素、胰岛素样生长因子1和胰岛素受体的减少,tau蛋白和糖原合成酶激酶3β的增加,这表明AD患者的大脑代谢受损。鉴于这些证据,在本研究中,我们采用基于定量质谱的方法研究了两种致肥性饮食,高脂肪饮食(HFD)和高血糖饮食(HGD)喂养的小鼠的大脑,并与标准饮食(SD)喂养的小鼠进行了比较。此外,还研究了翻译后修饰蛋白(磷酸化和n链糖基化)。这项研究的目的是确定大脑中存在的蛋白质,这些蛋白质会根据老鼠的饮食改变它们的表达。我们相信,其中一些变化将突出肥胖症与脑损伤之间的联系途径和分子机制。本研究结果表明,肥胖小鼠大脑中线粒体和代谢蛋白与细胞骨架蛋白一起改变了它们的翻译后状态。具体而言,与SD相比,在喂食致肥性饮食的小鼠中,参与代谢途径和线粒体功能的蛋白质主要下调。这些变化表明肥胖小鼠的新陈代谢和线粒体活性降低。其中一些蛋白质,如PGM1和MCT1,也被证明与脑损伤有关。这些结果可能会揭示肥胖和脑损伤之间已经得到充分研究的相关性。这里提出的结果与之前的发现一致,旨在为饮食引起的肥胖和脑损伤之间的联系开辟新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nutrition and Metabolic Insights
Nutrition and Metabolic Insights NUTRITION & DIETETICS-
CiteScore
3.30
自引率
0.00%
发文量
27
审稿时长
8 weeks
期刊介绍: Nutrition and Metabolic Insights is a peer-reviewed, open-access online journal focusing on all aspects of nutrition and metabolism. This encompasses nutrition, including the biochemistry of metabolism, exercise and associated physical processes and also includes clinical articles that relate to metabolism, such as obesity, lipidemias and diabetes. It includes research at the molecular, cellular and organismal levels. This journal welcomes new manuscripts for peer review on the following topics: Nutrition, including the biochemistry of metabolism, Exercise and associated physical processes, Clinical articles that relate to metabolism, such as obesity, lipidemias and diabetes, Research at the molecular, cellular and organismal levels, Other areas of interest include gene-nutrient interactions, the effects of hormones, models of metabolic function, macronutrient interactions, outcomes of changes in diet, and pathophysiology.
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