Benzophenanthridine alkaloids of Chelidonium majus .1. Inhibition of 5- and 12-lipoxygenase by a non-redox mechanism

被引:77
作者
Vavreckova, C
Gawlik, I
Muller, K
机构
[1] UNIV REGENSBURG,INST PHARM,D-93040 REGENSBURG,GERMANY
[2] PALACKY UNIV,INST MED CHEM,OLOMOUC 77515,CZECH REPUBLIC
关键词
anti-inflammatory activity; chelerythrine; chelidonine; Chelidonium majus L; Papaveraceae; 5-lipoxygenase; 12-lipoxygenase; sanguinarine;
D O I
10.1055/s-2006-957924
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The benzophenanthridine alkaloids sanguinarine and chelerythrine of Chelidonium majus, L. (Papaveraceae), are potent inhibitors of 5-lipoxygenase in polymorphonuclear leukocytes and 12-lipoxygenase in mouse epidermis, while the activity of soybean lipoxygenase is not influenced, The extract of the herb of Ch. majos also inhibits the 5-LO enzyme. Chelidonine, which cannot form pseudobases, is inactive against LO enzymes. Pro- and antioxidant actions of benzophenanthridine alkaloids can be excluded from the lack of deoxyribose degradation, reactivity against free radicals and inhibition of lipid peroxidation, suggesting that the inhibitory effects against LO enzymes appear to be due to specific enzyme interaction rather than a nonspecific redox mechanism.
引用
收藏
页码:397 / 401
页数:5
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