Inhibition of human low density lipoprotein oxidation by flavonols and their glycosides

被引:63
作者
Hou, LF [1 ]
Zhou, B [1 ]
Yang, L [1 ]
Liu, ZL [1 ]
机构
[1] Lanzhou Univ, Natl Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
low density lipoproteins; antioxidation; flavonol; glycoside;
D O I
10.1016/j.chemphyslip.2004.02.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antioxidative effects of the flavonols and their glycosides, i.e., quercetin (Q), quercetin galactopyranoside (QG), quercetin rhamnolpyranoside (QR), rutin (R), morin (MO), myrecetin (MY), kaempferol (K) and kaempferol glucoside (KG), against free radical initiated peroxidation of human low density lipoprotein (LDL) were Studied. The peroxidation was initiated either by a water-soluble initiator 2,2'-azobis(2-amidino propane hydrochloride) (AAPH), or by cupric ion (Cu2+). The reaction kinetics were monitored either by the uptake of oxygen and the depletion of a-tocopherol (TOH) presented in the native LDL, or by the formation of thiobarbituric acid reactive Substances (TBARS). Kinetic analysis of the antioxidation process demonstrates that these flavonols and their glycosides are effective antioxidants against AAPH- and Cu2+ -initiated LDL peroxidation, the flavonols bearing ortho-dihydroxyl groups possess significantly higher antioxidant activity than those bearing no such functionalities, and the glycosides are less active than their parent aglycones. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:209 / 219
页数:11
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