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Modulation of the Liver Protein Carbonylome by the Combined Effect of Marine Omega-3 PUFAs and Grape Polyphenols Supplementation in Rats Fed an Obesogenic High Fat and High Sucrose Diet

机译:食用肥胖高脂高糖饮食的大鼠海洋中Omega-3 PUFA和葡萄多酚的联合作用对肝脏蛋白羰基酶的调节

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摘要

Diet-induced obesity has been linked to metabolic disorders such as cardiovascular diseases and type 2 diabetes. A factor linking diet to metabolic disorders is oxidative stress, which can damage biomolecules, especially proteins. The present study was designed to investigate the effect of marine omega-3 polyunsaturated fatty acids (PUFAs) (eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)) and their combination with grape seed polyphenols (GSE) on carbonyl-modified proteins from plasma and liver in Wistar Kyoto rats fed an obesogenic diet, namely high-fat and high-sucrose (HFHS) diet. A proteomics approach consisting of fluorescein 5-thiosemicarbazide (FTSC) labelling of protein carbonyls, visualization of FTSC-labelled protein on 1-DE or 2-DE gels, and protein identification by MS/MS was used for the protein oxidation assessment. Results showed the efficiency of the combination of both bioactive compounds in decreasing the total protein carbonylation induced by HFHS diet in both plasma and liver. The analysis of carbonylated protein targets, also referred to as the ‘carbonylome’, revealed an individual response of liver proteins to supplements and a modulatory effect on specific metabolic pathways and processes due to, at least in part, the control exerted by the supplements on the liver protein carbonylome. This investigation highlights the additive effect of dietary fish oils and grape seed polyphenols in modulating in vivo oxidative damage of proteins induced by the consumption of HFHS diets.
机译:饮食引起的肥胖与代谢性疾病(如心血管疾病和2型糖尿病)有关。饮食与代谢紊乱有关的一个因素是氧化应激,氧化应激会破坏生物分子,尤其是蛋白质。本研究旨在研究海洋omega-3多不饱和脂肪酸(PUFAs)(二十碳五烯酸(EPA)和二十二碳六烯酸(DHA))及其与葡萄籽多酚(GSE)结合对血浆中羰基修饰蛋白的影响Wistar Kyoto大鼠的肝脏和肝脏喂养了致肥胖饮食,即高脂和高蔗糖(HFHS)饮食。蛋白质组学方法由蛋白质羰基的荧光素5-硫代氨基脲(FTSC)标记,在1-DE或2-DE凝胶上可视化FTSC标记的蛋白质以及通过MS / MS鉴定蛋白质组成,用于蛋白质氧化评估。结果表明,两种生物活性化合物的组合可有效减少HFHS饮食在血浆和肝脏中诱导的总蛋白质羰基化。对羰基化蛋白质靶标(也称为“羰基蛋白质组”)的分析显示,肝脏蛋白质对补充剂的个体反应以及对特定代谢途径和过程的调节作用,至少部分地是由于补充剂对蛋白质的控制作用肝蛋白羰基这项研究突出了膳食鱼油和葡萄籽多酚在调节因食用HFHS饮食引起的蛋白质体内氧化损伤中的加和作用。

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