THE CORRELATION BETWEEN ACTIVE OXYGENS SCAVENGING AND ANTIOXIDATIVE EFFECTS OF FLAVONOIDS

被引:784
作者
HANASAKI, Y
OGAWA, S
FUKUI, S
机构
[1] Department of Public Health Sciences, Kyoto Pharmaceutical University 5, Yamashina-ku, Kyoto, Nakauchi-cho, Misasagi
关键词
FLAVONOIDS; HYDROXYL RADICAL; SCAVENGER; LIPID PEROXIDATION; FREE RADICALS;
D O I
10.1016/0891-5849(94)90202-X
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
The abilities of 15 flavonoids as a scavenger of active oxygens (hydroxyl radical and superoxide anion) were studied. Hydroxyl radical ((OH)-O-.) was generated by the Fenton system, and assayed by the determination of methanesulfinic acid (MSA) formed from the reaction of dimethyl sulfoxide (DMSO) with (OH)-O-.. (+)-Catechin, (-)-epicatechin, 7,8-dihydroxy flavone, and rutin showed the (OH)-O-. scavenging effect 100-300 times superior to that of mannitol, a typical (OH)-O-. scavenger. The other flavonoids showed no (OH)-O-. scavenging effect at their concentrations up to 50 mu M. Baicalein, quercetin, morin, and myricetin unexpectedly increased the (OH)-O-. production in the Fenton system. The flavonoids tested now, except monohydroxy flavones, were more or less inhibitive to the superoxide anion (Oz) generation in the hypoxanthine-xanthine oxidase system. A great part of this inhibitory effect was likely owing to suppression of xanthine oxidase activity by the flavonoids. The flavonoids, which scavenged (OH)-O-. or O-2(-) , were necessarily antioxidants to the peroxidation of methyl linoleate. However, there was a type of flavonoid such as morin, which have neither (OH)-O-. nor O-2(-) scavenging effect, but was a strong antioxidant.
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页码:845 / 850
页数:6
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