KMID : 0385219990090010025
|
|
Korean Journal of Gerontology 1999 Volume.9 No. 1 p.25 ~ p.30
|
|
Effect of Flavonoids on Metal-Catalyzed Glyoxal Formation from Glucose
|
|
Song Dong-Up
So Keum-Young
Joung Young-Do Yang Sung-Yeul Ahn Bong-Whan
|
|
Abstract
|
|
|
The inhibitory effects of flavonoids on glyoxal formation from glucose by metal-catalyzed oxidation (MCO) systems were examined. The flavonoids tested were as follows: EGCG, ECG, EGC, EC, myricetin, kaempferol, quercetin, silymarin, luteolin, hesperidin, naringenin, apigenin and genistein. And two MCO systems,0.3 ¥ìM FeSO©þ/1 mM ascorbate and 0.1 ¥ìM CuSO©þ/1 mM ascorbate, were used since, at these concentrations, the MCO systems were found to stimulate maximally the glyoxal formation from glucose. The results were as follows: 1. EGCG, ECG, myricetin, kaempferol, quercetin, silymarin, and luteolin could inhibit the glyoxal formation by CuSO©þ/ascorbate, with values of 0.6-25 ¥ìM. In particular, EGCG, ECG and myricetin could inhibit very effectively the glyoxal formation by CuSO©þ/ascorbate, with IC50 values less than 1 ¥ìM. 2. EGCG, ECG, and myricetin could inhibit the glyoxal formation by FeSO©þ/ascorbate, with IC50 valuers of 6.5 -51 ¥ìm. 3. Flavouoids inhibited more potently the glyoxal formation by CuSO©þ/ascorbate than that by FeSO©þ/ascorbate. These results suggest that some flavonoids such as EGCG, ECG, and myricetin may be useful inhibitors of glucose oxidation occurring in vivo.
|
|
KEYWORD
|
|
Flavonoids, Glyoxal, Dicarbonyl, Glucose oxidation, Metal-catalyzed oxidation(MCO), AGE
|
|
FullTexts / Linksout information
|
|
|
|
Listed journal information
|
|
|
|