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食用植物产品抗氧化活性的筛选:低密度脂蛋白氧化测定法、DPPH自由基清除测定法和福林-西奥尔特法的比较

Screening for antioxidant activity in edible plant products: comparison of low-density lipoprotein oxidation assay, DPPH radical scavenging assay, and Folin-Ciocalteu assay.

作者信息

Katsube Takuya, Tabata Hiromasa, Ohta Yukari, Yamasaki Yukikazu, Anuurad Erdembileg, Shiwaku Kuninori, Yamane Yosuke

机构信息

Shimane Institute for Industrial Technology, 1 Hokuryo-cho, Matsue City, Shimane, 690-0816, Japan.

出版信息

J Agric Food Chem. 2004 Apr 21;52(8):2391-6. doi: 10.1021/jf035372g.

Abstract

Oxidation of low-density lipoprotein (LDL) has been implicated in atherogenesis. Antioxidants that prevent LDL from oxidizing may reduce atherosclerosis. This study investigated LDL antioxidant activity in edible plant products for development of dietary supplementation to prevent atherosclerosis. Fifty-two kinds of edible plants were extracted using 70% aqueous ethanol solution, and the antioxidant activity of the extracts, which inhibit human LDL oxidation induced by copper ion, was determined on the basis of the oxidation lag time and represented as epigallocatechin 3-gallate equivalent. 1,1-Diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity and total phenolic content were also measured for comparisons with antioxidant activity in LDL. Plant products showing the greatest activity in LDL oxidation assay were akamegashiwa (Mallotus japonicus) leaf, Japanese privet (Ligustrum japonicum) leaf, green tea [Camellia sinensis (L.) O. Kuntze], and astringent persimmon (Diospyros kaki). The present study revealed high levels of LDL antioxidant activity in plant products for which such activity levels are underestimated in the DPPH radical scavenging assay and Folin-Ciocalteu assay.

摘要

低密度脂蛋白(LDL)的氧化与动脉粥样硬化的发生有关。防止LDL氧化的抗氧化剂可能会减轻动脉粥样硬化。本研究调查了可食用植物产品中的LDL抗氧化活性,以开发预防动脉粥样硬化的膳食补充剂。用70%乙醇水溶液提取了52种可食用植物,并根据氧化滞后时间测定提取物抑制铜离子诱导的人LDL氧化的抗氧化活性,以表没食子儿茶素3-没食子酸酯当量表示。还测定了1,1-二苯基-2-苦基肼(DPPH)自由基清除活性和总酚含量,以便与LDL中的抗氧化活性进行比较。在LDL氧化试验中表现出最大活性的植物产品是秋枫叶、日本女贞叶、绿茶[茶树(L.)O. Kuntze]和涩柿。本研究表明,植物产品中LDL抗氧化活性水平较高,而在DPPH自由基清除试验和福林-酚试剂法测定中,这些活性水平被低估。

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