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多酚在对心脏病具有保护作用的生物学相关浓度下与低密度脂蛋白结合。

Polyphenols bind to low density lipoprotein at biologically relevant concentrations that are protective for heart disease.

机构信息

Department of Chemistry, Loyola Science Center, University of Scranton, Scranton, PA, 18510, USA.

Department of Chemistry, University of Calgary, 2500 University Drive, NW, Calgary, Alberta, T2N1N4, Canada.

出版信息

Arch Biochem Biophys. 2020 Nov 15;694:108589. doi: 10.1016/j.abb.2020.108589. Epub 2020 Sep 30.

Abstract

There is ample evidence in the epidemiological literature that polyphenols, the major non-vitamin antioxidants in plant foods and beverages, have a beneficial effect on heart disease. Until recently other mechanisms which polyphenols exhibit such as cell signaling and regulating nitric oxide bioavailability have been investigated. The oxidation theory of atherosclerosis implicates LDL oxidation as the beginning step in this process. Nine polyphenols from eight different classes and several of their O-methylether, O-glucuronide and O-sulfate metabolites have been shown in this study to bind to the lipoproteins and protect them from oxidation at lysosomal/inflammatory pH (5.2), and physiological pH (7.4). Polyphenols bind to the apoprotein at pH 7.4 with K > 10 M and the number of molecules of polyphenols bound per LDL particle under saturation conditions varied from 0.4 for ferulic acid to 13.1 for quercetin. Competition studies between serum albumin and LDL show that substantial lipoprotein binding occurs even in the presence of a great molar excess of albumin, the major blood protein. These in vitro results are borne out by published human supplementation studies showing that polyphenol metabolites from red wine, olive oil and coffee are found in LDL even after an overnight fast. A single human supplementation with various fruit juices, coffee and tea also produced an ex vivo protection against lipoprotein oxidation under postprandial conditions. This in vivo binding is heart-protective based on published olive oil consumption studies. Relevant to heart disease, we hypothesize that the binding of polyphenols and metabolites to LDL functions as a transport mechanism to carry these antioxidants to the arterial intima, and into endothelial cells and macrophages. Extracellular and intracellular polyphenols and their metabolites are heart-protective by many mechanisms and can also function as potent "intraparticle" and intracellular antioxidants due to their localized concentrations that can reach as high as the micromolar level. Low plasma concentrations make polyphenols and their metabolites poor plasma antioxidants but their concentration in particles such as lipoproteins and cells is high enough for polyphenols to provide cardiovascular protection by direct antioxidant effects and by other mechanisms such as cell signaling.

摘要

有大量证据表明,多酚是植物性食物和饮料中主要的非维生素抗氧化剂,对心脏病有有益影响。直到最近,人们才开始研究多酚所表现出的其他机制,如细胞信号传递和调节一氧化氮生物利用度。动脉粥样硬化的氧化理论暗示 LDL 氧化是这一过程的起始步骤。本研究表明,来自 8 个不同类别的 9 种多酚及其 O-甲基醚、O-葡萄糖醛酸苷和 O-硫酸盐代谢物,能够与脂蛋白结合,并在溶酶体/炎症 pH(5.2)和生理 pH(7.4)下保护它们免受氧化。在 pH 7.4 时,多酚与载脂蛋白的结合常数大于 10 M,在饱和条件下,每个 LDL 颗粒结合的多酚分子数从阿魏酸的 0.4 到槲皮素的 13.1 不等。血清白蛋白与 LDL 之间的竞争研究表明,即使在白蛋白(主要的血液蛋白)存在巨大摩尔过量的情况下,也会发生大量的脂蛋白结合。这些体外结果与已发表的人类补充研究结果一致,这些研究表明,即使在禁食一夜后,红酒、橄榄油和咖啡的多酚代谢物也能在 LDL 中被发现。单次饮用各种果汁、咖啡和茶也能在餐后条件下对脂蛋白氧化产生体外保护作用。基于已发表的橄榄油消费研究,这种体内结合具有心脏保护作用。与心脏病相关的是,我们假设多酚及其代谢物与 LDL 的结合作为一种运输机制,将这些抗氧化剂输送到动脉内膜,并进入内皮细胞和巨噬细胞。细胞外和细胞内的多酚及其代谢物通过多种机制具有心脏保护作用,由于其局部浓度可达微摩尔水平,因此也可以作为有效的“颗粒内”和细胞内抗氧化剂。低血浆浓度使多酚及其代谢物成为较差的血浆抗氧化剂,但它们在脂蛋白和细胞等颗粒中的浓度足以使多酚通过直接抗氧化作用和细胞信号传递等其他机制提供心血管保护。

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