Determination of the antigenotoxic potencies of some luteolin derivatives by using a eukaryotic cell system, Saccharomyces cerevisiae

Food Chemistry

Volumn 141, Issue 1, 2013, Pages 366-372

  Orhan, Furkan ^a,b   Gulluce, Medine ^b   Ozkan, Hakan ^c   Alpsoy, Lokman ^d  

^a AGRI IBRAHIM CECEN UNIVERSITY   (Turkey)

^b ATATÜRK UNIVERSITY   (Turkey)

^c ERZINCAN UNIVERSITY   (Turkey)

^d FATIH UNIVERSITY   (Turkey)

Author keywords

Antimutagenicity; Luteolin derivatives; Saccharomyces cerevisiae; Yeast DEL assay

Indexed keywords

ASSAYS; CARBOHYDRATES; MUTAGENESIS; YEAST;

ANTI-MUTAGENICITY; ANTIGENOTOXIC; ANTIMUTAGENIC; ETHYL METHANESULFONATE; EUKARYOTIC CELLS; GLUCURONIDES; INHIBITION RATE; RECOMBINATION EVENTS;

FLAVONOIDS;

ACRIDINE; LUTEOLIN; LUTEOLIN 7 GLUCOSIDE; LUTEOLIN 7 GLUCURONIDE; LUTEOLIN 7 RUTINOSIDE; MESYLIC ACID ETHYL ESTER; MUTAGENIC AGENT; UNCLASSIFIED DRUG;

ANTIOXIDANT ACTIVITY; ARTICLE; DRUG DETERMINATION; EUKARYOTIC CELL; GENE DELETION; GENETIC RECOMBINATION; MUTATION INHIBITION; NONHUMAN; SACCHAROMYCES CEREVISIAE;

EUKARYOTA; SACCHAROMYCES CEREVISIAE;

EID: 84877611206     PISSN: 03088146     EISSN: 18737072     Source Type: Journal    
DOI: 10.1016/j.foodchem.2013.02.089     Document Type: Article

References (31)

1. Achary, V. M. M., & Panda, B. B. (2010). Aluminium-induced DNA damage and adaptive response to genotoxic stress in plant cells are mediated through reactive oxygen intermediates. Mutagenesis, 25, 201-209.
2. Anderson, I. B., Mullen, W. H., & Meeker, J. E. (1996). Pennyroyal toxicity: Measurement of toxic metabolite levels in two cases and review of the literature. Annals of International Medicine, 124, 726-734. (Pubitemid 26117921)
3. Bhat, S., Maheshwari, P., Kumar, S., & Kumar, A. (2002). Mentha species: In vitro regeneration and genetic transformation. Molecular Biology Today, 3, 11-23.
4. Brennan, R. J., & Schiestl, R. H. (2004). Detecting carcinogens with the yeast DEL assay. Methods in Molecular Biology, 262, 111-124.
5. Brusselmans, K., Vrolix, R., Verhoeven, G., & Swinnen, J. V. (2005). Induction of cancer cell apoptosis by flavonoids is associated with their ability to inhibit fatty acid synthase activity. Journal of Biological Chemistry, 280, 5636-5645. (Pubitemid 40280043)
6. Buryskova, B., Hilscherova, K., Blaha, L., Marsalek, B., & Holoubek, I. (2006). Toxicity and modulations of biomarkers in Xenopus laevis embryos exposed to polycyclic aromatic hydrocarbons and their N-heterocyclic derivatives. Environmental Toxicology, 21, 590-598. (Pubitemid 44788790)
7. Cakir, A., Mavi, A., Kazaz, C, Yildirim, A., & Kufrevioglu, O. I. (2006). Antioxidant activities of the extracts and components of Teucrium orientale L. var orientale. Turkish Journal of Chemistry, 30, 483-494. (Pubitemid 44525609)
8. Cantero, G., Campanella, C, Mateos, C, & Cortes, F. (2006). Topoisomerase II inhibition and high yield of endoreduplication induced by the flavonoids luteolin and quercetin. Mutagenesis, 21, 321-325. (Pubitemid 44546415)
9. Chen, C. Y., Peng, W. H., Tsai, K. D., & Hsu, S. L. (2007). Luteolin suppresses inflammation-associated gene expression by blocking NF-kappaB and AP-1 activation pathway in mouse alveolar macrophages. Life Sciences, 81, 1602-1614.
10. Ferguson, L. R., & Denny, W. A. (2007). Genotoxicity of non-covalent interactions: DNA intercalators. Mutation Research, 623, 14-23. (Pubitemid 47368577)
11. Guha, B., & Khuda-Bukhsh, A. R. (2003). Ameliorating effect of β-carotene on ethylmethane sulphonate-induced genotoxicity in the fish Oreochromis mossambicu. Mutation Research, 542, 1-13. (Pubitemid 37486092)
12. Gulluce, M., Sahin, F., Sokmen, M., Ozer, H., Daferera, D., Sokmen, A., et al. (2007). Antimicrobial and antioxidant properties of the essential oils and methanol extract from Mentha longifolia L. ssp. longifolia. Food Chemistry, 103, 1449-1456. (Pubitemid 46467142)
13. Ju, W., Wang, X., Shi, H., Chen, W., Belinsky, S. A., & Lin, Y. (2007). A critical role of luteolin-induced reactive oxygen species in blockage of tumor necrosis factor-activated nuclear factor kappaB pathway and sensitization of apoptosis in lung cancer cells. Molecular Pharmacology, 71, 1381-1388. (Pubitemid 46658691)
14. Karrasch, T., Kim, J. S., Jang, B. I., & Jobin, C. (2007). The flavonoid luteolin worsens chemical-induced colitis in NF-kappaB (EGFP) transgenic mice through blockade of NF-kappaB-dependent protective molecules. PLoS ONE, 2, 596.
15. Kuroda, Y., & Hara, Y. (1999). Antimutagenic and anticarcinogenic activity of tea polyphenols. Mutation Research, 436, 69-97. (Pubitemid 29044047)
16. Lemańska, K., Van der Woude, H., Szymusiak, H., Boersma, M. G., Gliszczyńska-Świgło, A., Rietjens, I. M. C. M., et al. (2004). The effect of catechol O-methylation on radical scavenging characteristic of quercetin and luteolin - A mechanistic insight. Free Radical Research, 38, 639-647. (Pubitemid 38697097)
17. Nagy, M., Križková, L., Mučaji, P., Kontšeková, Z., Šeršeň, S., & Krajčovič, J. (2009). Antimutagenic activity and radical scavenging activity of water infusions and phenolics from Ligustrum plants leaves. Molecules, 14, 509-518.
18. Nissler, L., Gebhardt, R., & Berger, S. (2004). Flavonoid binding to a multi-drug-resistance transporter protein: An STD-NMR study. Analytical and Bioanalytical Chemistry, 379, 1045-1049. (Pubitemid 40877535)
19. Odontuya, G., Hoult, J. R., & Houghton, P. J. (2005). Structure-activity relationship for antiinflammatory effect of luteolin and its derived glycosides. Phytotherapy Research, 19, 782-786. (Pubitemid 41571428)
20. Orhan, F., Baris, O., Yanmis, D., Bal, T., Guvenalp, Z., & Gulluce, M. (2012). Isolation of some luteolin derivatives from Mentha longifolia (L.) Hudson subsp. longifolia and determination of their genotoxic potencies. Food Chemistry, 135, 764-769.
21. Paglia, D. E., & Valentine, W. N. (1967). Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. Journal for Laboratory and Clinical Medicine, 70, 158-169.
22. Ringl, A., Prinz, S., Huefner, A., Kurzmann, M., & Kopp, B. (2007). Chemosystematic value of flavonoids from Crataegus x macrocarpa (Rosaceae) with special emphasis on(R)- and (S)-eriodictyol-7-O-glucuronide and luteolin-7-O-glucuronide. Chemistry & Biodiversity, 4, 154-162. (Pubitemid 46929185)
23. Rodriguez, C. E., Shinyashiki, M., Froines, J., Yu, R. C., Fukuto, J. M., & Cho, A. K. (2004). An examination of quinone toxicity using the yeast Saccharomyces cerevisiae model system. Toxicology, 201, 185-196. (Pubitemid 39023945)
24. Samejima, K., Kanazawa, K., Ashida, H., & Danno, G.-I. (1995). Luteolin: A strong antibutagen against dietary carcinogen, Trp-P-2, in peppermint, sage, and thyme. Journal of Agricultural and Food Chemistry, 43, 410-414.
25. Shi, R., Huang, Q., Zhu, X., Ong, Y. B., Zhao, B., Lu, J., et al. (2007). Luteolin sensitizes the anticancereffect of cisplatin via c-Jun NH2-terminal kinase-mediated p53 phosphorylation and stabilization. Molecular Cancer Therapeutics, 6, 1338-1347. (Pubitemid 46711997)
26. Shi, R. X., Ong, C. N., & Shen, H. M. (2004). Luteolin sensitizes tumor necrosis factor-alpha-induced apoptosis in human tumor cells. Oncogene, 23, 7712-7721.
27. Sugihara, N., Arakawa, T., Ohnishi, M., & Furuno, K. (1999). Anti- and pro-oxidative effects of flavonoids on metalinduced lipid hydroperoxide-dependent lipid peroxidation in cultured hepatocytes loaded with alphalinolenic acid. Free Radical Biology and Medicine, 27, 1313-1323. (Pubitemid 30001494)
28. Tietze, F. (1969). Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: Applications to mammalian blood and other tissues. Analytical Biochemistry, 27, 502-522.
29. Tirmenstein, M. A., Nicholls-Grzemski, F. A., Zhang, J. G., & Fariss, M. W. (2000). Glutathione depletion and the production of reactive oxygen species in isolated hepatocyte suspensions. Chemico-Biological Interactions, 127, 201-217. (Pubitemid 30624156)
30. Tormakangas, L., Vuorela, P., Saario, E., Leinonen, M., Saikku, P., & Vuorela, H. (2005). In vivo treatment of acute Chlamydia pneumoniae infection with the flavonoids quercetin and luteolin and an alkyl gallate, octyl gallate, in a mouse model. Biochemical Pharmacology, 70, 1222-1230. (Pubitemid 41317516)
31. Wang, M., Simon, J. E., Aviles, I. F., He, K., Zheng, Q. Y., & Tadmor, Y. (2003). Analysis of actioxidative phenolic compounds in Artichoke (Cynara scolymus L.). Journal of Agricultural and Food Chemistry, 51, 601-608.