Antigenotoxic effect of extract from Cynara cardunculus L

The extract of artichoke Cynara cardunculus L. (CCE) was investigated for its potential antigenotoxic and antioxidant effects using four experimental model systems. In the Saccharomyces cerevisiae mutagenicity/antimutagenicity assay, CCE significantly reduced the frequency of 4‐nitroquinoline‐N‐oxid...

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Published inPhytotherapy research Vol. 22; no. 1; pp. 77 - 81
Main Authors Miadokova, E., Nadova, S., Vlckova, V., Duhova, V., Kopaskova, M., Cipak, L., Rauko, P., Mucaji, P., Grancai, D.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.01.2008
Wiley
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Summary:The extract of artichoke Cynara cardunculus L. (CCE) was investigated for its potential antigenotoxic and antioxidant effects using four experimental model systems. In the Saccharomyces cerevisiae mutagenicity/antimutagenicity assay, CCE significantly reduced the frequency of 4‐nitroquinoline‐N‐oxide‐induced revertants at the ilv1 locus and mitotic gene convertants at the trp5 locus in the diploid Saccharomyces cerevisiae tester strain D7. In the simultaneous toxicity and clastogenicity/anticlastogenicity assay, it exerted an anticlastogenic effect against N‐nitroso‐N′‐methylurea‐induced clastogenicity in the plant species Vicia sativa L. On the contrary, despite CCE not being mutagenic itself, in the preincubation Ames assay with metabolic activation, it significantly increased the mutagenic effect of 2‐aminofluorene in the bacterial strain Salmonella typhimurium TA98. In the 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) free radical scavenging assay, CCE exhibited considerable antioxidant activity. The SC50 value representing 0.0054% CCE corresponds to an antioxidant activity of 216.8 µm ascorbic acid which was used as a reference compound. Although the mechanism of CCE action still remains to be elucidated, different possible mechanisms are probably involved in the CCE antigenotoxic effects. It could be concluded that CCE is of particular interest as a suitable candidate for an effective chemopreventive agent. Copyright © 2007 John Wiley & Sons, Ltd.
Bibliography:VEGA grants from the Ministry of Education of the Slovak Republic and Slovak Academy of Sciences - No. 1/2337/05; No. 1/4289/07; No. 2/7088/07; No. 1/0008/08
Research and Development Support Agency - No. APVT-20-002604
ArticleID:PTR2268
istex:4CC7C403F3DB399488AB602742738D96EE5A24C1
ark:/67375/WNG-9N50S44L-L
ISSN:0951-418X
1099-1573
DOI:10.1002/ptr.2268