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Chemical Modeling of Heme-Induced Lipid Oxidation in Gastric Conditions and Inhibition by Dietary Polyphenols

机译:血红素在胃中诱导脂质氧化和膳食多酚抑制的化学模型

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摘要

The gastric tract may be the first site exposed to diet-related oxidative stress. After food intake, dietary iron such as (met)myoglobin, the pigment of meat, oxygen, and polyunsaturated lipids come into close contact. The main goal of this work is the in vitro investigation of lipid oxidation taking place in the gastric compartment and its inhibition by dietary polyphenols. Oil-in-water emulsions stabilized either by bovine serum albumin (BSA) or egg yolk phospholipids (PL) were designed to model the gastric content. The metmyoglobin-initiated lipid oxidation led to the accumulation of lipid-derived conjugated dienes and volatile aldehydes. These reactions were faster in the BSA model than in the PL model, highlighting the influence of the interfacial composition. Quercetin, rutin, (+)-catechin, caffeic acid, and chlorogenic acid proved to be better inhibitors than a-tooopherol and ascorbic acid. Emulsions as models of the gastric environment are valuable tools to study the stability of macro-and micronutrients.
机译:胃道可能是暴露于饮食相关的氧化应激的第一个部位。食物摄入后,膳食铁(例如,肌红蛋白),肉类的色素,氧气和多不饱和脂质紧密接触。这项工作的主要目的是体外研究在胃室发生的脂质氧化及其是否被饮食中的多酚抑制。设计通过牛血清白蛋白(BSA)或蛋黄磷脂(PL)稳定的水包油乳剂来模拟胃内容物。肌红蛋白引发的脂质氧化导致脂质衍生的共轭二烯和挥发性醛的积累。这些反应在BSA模型中比在PL模型中更快,突出了界面组成的影响。槲皮素,芦丁,(+)-儿茶素,咖啡酸和绿原酸被证明是比α-萜烯醇和抗坏血酸更好的抑制剂。乳剂作为胃环境的模型是研究大量和微量营养素稳定性的有价值的工具。

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