Galvez J, de la Cruz J P, Zarzuelo A, Sanchez de la Cuesta F
Department of Pharmacology, School of Pharmacy, University of Granada, Spain.
Pharmacology. 1995 Aug;51(2):127-33. doi: 10.1159/000139325.
Eight flavonoids were tested for their antiperoxidative activities against lipid peroxidation induced in liver cell membranes either by nonenzymic way (ascorbic acid-Fe2+ system, FeAs) or by enzymic way (arachidonic acid, AA). When lipid peroxidation is induced by FeAs, the order in the inhibitory potency for the different flavonoids assayed is: (-)-epicatechin approximately luteolin > quercetin approximately (+)-catechin > delphinidin > kaempferol >> apigenin > naringenin. However, when lipid peroxidation is induced by AA, the potency order is markedly modified: delphinidin > (-)-epicatechin > (+)-catechin > kaempferol > quercetin > luteolin > naringenin > apigenin. These flavonoids were also tested for their influence on glutathione-related enzymes, which constitute one of the aim physiological antioxidant systems. It is concluded that the antiperoxidative effect shown by most of the flavonoids is exerted without modifying these enzymes.
测试了八种黄酮类化合物对通过非酶途径(抗坏血酸 - Fe2+ 系统,FeAs)或酶途径(花生四烯酸,AA)诱导的肝细胞膜脂质过氧化的抗过氧化活性。当由FeAs诱导脂质过氧化时,所测定的不同黄酮类化合物的抑制效力顺序为:(-)-表儿茶素≈木犀草素>槲皮素≈(+)-儿茶素>飞燕草素>山奈酚>>芹菜素>柚皮素。然而,当由AA诱导脂质过氧化时,效力顺序明显改变:飞燕草素>(-)-表儿茶素>(+)-儿茶素>山奈酚>槲皮素>木犀草素>柚皮素>芹菜素。还测试了这些黄酮类化合物对谷胱甘肽相关酶的影响,这些酶构成了目标生理抗氧化系统之一。得出的结论是,大多数黄酮类化合物所表现出的抗过氧化作用是在不改变这些酶的情况下发挥的。