Green tea polyphenols: Novel and potent inhibitors of squalene epoxidase

被引:129
作者
Abe, I
Seki, T
Umehara, K
Miyase, T
Noguchi, H
Sakakibara, J
Ono, T
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Shizuoka 4228526, Japan
[2] Niigata Univ, Sch Med, Niigata 9518510, Japan
关键词
D O I
10.1006/bbrc.2000.2217
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 green tea gallocatechins, (-)-epigallocatechin-3-O-gallate (EGCG)(IC50 = 0.69 mu M), (-)-gallocatechin-3-O-gallate (GCG)-(IC50 = 0.67 mu M), (-)-epicatechin-3-O-gallate (ECG) (IC50 = 1 3 mu M), and theasinensin A (IC50 = 0.13 mu M), were found to be potent and selective inhibitors of rat squalene epoxidase (SE), a rate-limiting enzyme of cholesterol biogenesis. On the other hand, flavan-3-ols without galloyl group at C-3 did not show significant enzyme inhibition. It was demonstrated for the first time that the cholesterol lowering effect of green tea may be attributed to their potent SE inhibition activities. Inhibition kinetics revealed that EGCG inhibited SE in noncompetitive (K-I = 0.74 mu M), and non-time-dependent manner. The potent enzyme inhibition would be caused by specific binding to the enzyme, and by scavenging reactive oxygen species required for the monooxygenase reaction. (C) 2000 Academic Press.
引用
收藏
页码:767 / 771
页数:5
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