Planta Med 1996; 62(5): 397-401
DOI: 10.1055/s-2006-957924
Paper

© Georg Thieme Verlag Stuttgart · New York

Benzophenanthridine Alkaloids of Chelidonium majus; I. Inhibition of 5- and 12-Lipoxygenase by a Non-Redox Mechanism

Ctirada Vavrečková1 , Ingo Gawlik2 , Klaus Müller2
  • 1Institute of Medical Chemistry, Palacký University, Hněvotínská 3, 77515 Olomouc, Czech Republic
  • 2Institute of Pharmacy, University of Regensburg, Universitätsstr. 31, D-93040 Regensburg, Germany
Further Information

Publication History

1996

1996

Publication Date:
04 January 2007 (online)

Abstract

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. majus 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.

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