Nagao A, Seki M, Kobayashi H
National Food Research Institute, Ministry of Agriculture, Forestry and Fisheries, Tsukuba, Ibaraki, Japan.
Biosci Biotechnol Biochem. 1999 Oct;63(10):1787-90. doi: 10.1271/bbb.63.1787.
Various dietary flavonoids were evaluated in vitro for their inhibitory effect on xanthine oxidase, which has been implicated in oxidative injury to tissue by ischemia-reperfusion. Xanthine oxidase activity was determined by directly measuring uric acid formation by HPLC. The structure-activity relationship revealed that the planar flavones and flavonols with a 7-hydroxyl group such as chrysin, luteolin, kaempferol, quercetin, myricetin, and isorhamnetin inhibited xanthine oxidase activity at low concentrations (IC50 values from 0.40 to 5.02 microM) in a mixed-type mode, while the nonplanar flavonoids, isoflavones and anthocyanidins were less inhibitory. These results suggest that certain flavonoids might suppress in vivo the formation of active oxygen species and urate by xanthine oxidase.
对多种膳食类黄酮进行了体外评估,以研究它们对黄嘌呤氧化酶的抑制作用,黄嘌呤氧化酶与缺血再灌注引起的组织氧化损伤有关。通过高效液相色谱法直接测量尿酸生成来测定黄嘌呤氧化酶活性。结构-活性关系表明,具有7-羟基的平面黄酮和黄酮醇,如白杨素、木犀草素、山奈酚、槲皮素、杨梅素和异鼠李素,在低浓度下(IC50值为0.40至5.02微摩尔)以混合型模式抑制黄嘌呤氧化酶活性,而非平面类黄酮、异黄酮和花青素的抑制作用较小。这些结果表明,某些类黄酮可能在体内抑制黄嘌呤氧化酶产生活性氧和尿酸。