Inhibitory effects of flavonoids on rabbit heart carbonyl reductase

被引:31
作者
Imamura, Y [1 ]
Migita, T [1 ]
Uriu, Y [1 ]
Otagiri, M [1 ]
Okawara, T [1 ]
机构
[1] Kumamoto Univ, Fac Pharmaceut Sci, Kumamoto 8620973, Japan
关键词
flavonoid; inhibition mechanism; rabbit heart carbonyl reductase; structure activity relationship; superoxide anion radical;
D O I
10.1093/oxfordjournals.jbchem.a022653
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 inhibitory effects of flavonoids (galangin, kaempferol, quercetin, myricetin, morin, and taxifolin) on rabbit heart carbonyl reductase (RHCR) were investigated using 4-benzoylpyridine (4BP) as the substrate. The stereochemical characteristics of the flavonoids were found to be a factor determining their inhibitory potencies toward RHCR, Furthermore, the lipophilicity, and the scavenging or antioxidative effects of the flavonoids were likely to complicate the structure-activity relationship of their inhibitory effects on RHCR, Quercetin inhibited RHCR uncompetitively with respect to NADPH and competitively with respect to 4BP, suggesting that it competes with 4BP at the substrate-binding site of RHCR. RHCR efficiently reduced benzoquinones (1,4-benzoquinone and 2-methyl-1,4-benzoquinone) and naphthoquinones (1,4-naphthoquinone and menadione), Galangin was a potent inhibitor of RHCR when menadione was used as the substrate, and prevented the formation of the superoxide anion radical in the presence of RHCR, NADPH, and menadione, Flavonoids may be useful compounds for suppressing the cardiotoxicity of quinones by inhibiting RHCR.
引用
收藏
页码:653 / 658
页数:6
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