Genotoxic Effects of Herbicide Illoxan (Diclofop-Methyl) on Allium cepa L.

The genotoxic potential of the commercial herbicide Illoxan (containing 284 g/L diclofop-methyl) was determined by using chromosome aberrations in Allium cepa root tip cells. The EC50 value was determined as 150.00 mg/L using a root growth inhibition test and then the roots were treated with 37.50, 75.00, and 150.00 mg/L concentrations for 12, 24, and 48 h. The results indicated that Illoxan significantly increased the abnormal cell frequency at all concentrations and treatment periods when compared with their controls, and this increase was dose-dependent for the 24 and 48 h treatments. On the other hand, Illoxan significantly decreased the mitotic index (MI) in all treatments when compared with their controls. The decrease in the mitotic index was slightly dose-dependent for the 24 and 48 h treatments. Illoxan did not affect the percentage of mitotic stages. For the pretreated root tips, Illoxan (except 37.50 mg/L at 12 and 24 h) significantly increased the frequency of abnormal cells in a dose-dependent manner. This study indicates that Illoxan decreased the mitotic index and produced clastogenic and aneugenic types of abnormalities in Allium cepa root tip cells. The data obtained in this study showed that plant bioassays can be used as an important test battery to detect possible genotoxicity of chemicals.

Genotoxic Effects of Herbicide Illoxan (Diclofop-Methyl) on Allium cepa L.

The genotoxic potential of the commercial herbicide Illoxan (containing 284 g/L diclofop-methyl) was determined by using chromosome aberrations in Allium cepa root tip cells. The EC50 value was determined as 150.00 mg/L using a root growth inhibition test and then the roots were treated with 37.50, 75.00, and 150.00 mg/L concentrations for 12, 24, and 48 h. The results indicated that Illoxan significantly increased the abnormal cell frequency at all concentrations and treatment periods when compared with their controls, and this increase was dose-dependent for the 24 and 48 h treatments. On the other hand, Illoxan significantly decreased the mitotic index (MI) in all treatments when compared with their controls. The decrease in the mitotic index was slightly dose-dependent for the 24 and 48 h treatments. Illoxan did not affect the percentage of mitotic stages. For the pretreated root tips, Illoxan (except 37.50 mg/L at 12 and 24 h) significantly increased the frequency of abnormal cells in a dose-dependent manner. This study indicates that Illoxan decreased the mitotic index and produced clastogenic and aneugenic types of abnormalities in Allium cepa root tip cells. The data obtained in this study showed that plant bioassays can be used as an important test battery to detect possible genotoxicity of chemicals.

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  • Grant WF. Higher plant assays for the detection of chromosomal aberrations and gene mutations - a brief historical background on their use for screening and monitoring environmental chemicals. Mutat Res 426: 107-112, 1999. 7. Ma TH. The international program on plant bioassays and the report of the follow-up study after the hands-on workshop in China. Mutat Res 426: 103-106, 1999. 8. Yi HL, Meng ZQ. Genotoxicity of hydrated sulfur dioxide on root tips of Allium sativum and Vicia faba. Mutat Res 537: 109- 114, 2003. 9. Tomlin CDS (ed.). The Pesticide Manual 13thEd. BCPC, 2003.
  • United States Environmental Protection Agency (USEPA). Prevention, Pesticides and Toxic Substances (7508C) R.E.D. FACTS Diclofop-Methyl. EPA-738-F-00-007, 2000.
  • Cancer Assessment Review Committee (CARC). Evaluation of the Carcinogenic Potential of Diclofop-methyl. P.C. Code: 110902, 2000.
  • Bolle P, Mastrangelo S, Tucci P et al. Clastogenicity of atrazine assessed with the Allium cepa test. Environ Mol Mutagen 43: 137-141, 2004.
  • Fiskesjö G. The Allium test as a standart in environmental monitoring. Hereditas 102: 99-112, 1985.
  • Nicoloff H, Kappas A. Benomyl induced mitotic disturbances in Hordeum vulgare. Mutat Res 189: 271-275, 1987.
  • Grisolia CK, Bilich MR, Formigli LM. A comparative toxicologic and genotoxic study of the herbicide arsenal, its active ingredient imazapyr, and the surfactant nonylphenol ethoxylate. Ecotox Environ Safety 59: 123-126, 2004.
  • Shcneiderman MH, Dewey WC, Highfıeld DP. Inhibition of DNA synthesis in synchronized Chinese hamster cell treated in G1with cycloheximide. Exp Cell Res 67: 147-155, 1971.
  • Van’t Hof J. The action of IAA and kinetin on the mitotic cycle of proliferative and stationary phase excised root meristem. Exp Cell Res 51: 167-176, 1968.
  • Sudhakar R, Ninge Gowda KN, Venu G. Mitotic abnormalities induced by silk dyeing industry effluents in the cell of Allium cepa. Cytologia 66: 235-239, 2001.
  • Chand S, Roy SC. Effects of herbicide 2,4-dinitrophenol on mitosis, DNA, RNA and protein synthesis in Nigella sativa L. Biol Plantarum 23: 198-202, 1981.
  • Ateeq B, Abdul FM, Niamat AM et al. Clastogenicity of Pentachlorophenol, 2,4-D and Butachlor evaluated by Allium root tip test. Mutat Res 514: 105-113, 2002.
  • Haliem AS. Cytological effects of the herbicide sencor on mitosis of Allium cepa. Egypt J Bot 33: 93-104, 1990.
  • Murli H. Screening assay for chromosomal aberrations in Chinese hamster ovary (CHO) cells with argentyn 23, Final Report, 2003.
  • Rencüzoğulları E, İla HB, Kayraldız A et al. The genotoxic effect of the new acaricide etoxazole. Russ J Genet 40(11): 1300-1304, 2004.
  • Valeminsky J, Gicher T. Mutagenic activity of promutagens in plants: indirect evidence of their activation. Mutat Res 197: 221- 242, 1988.
  • Gentile JM, Gentile GJ, Bultman J et al. An evaluation of the genotoxic properties of insecticides following plant and animal activation. Mutat Res 101: 19-29, 1982.
  • Plewa MJ, Wagner ED, Gentile GJ et al. An evaluation of the genotoxic properties of herbicides following plant and animal activation. Mutat Res 136: 233-245, 1984.
  • Calderon-Segura ME, Gomez-Arroyo S, Villalobos-Pietrini R et al. In vivo and in vitro promutagen activation by Vicia faba of thiocarbamate herbicides molinate and butylate to products inducing sister chromatid exchanges in human lymphocyte cultures. Mutat Res 438: 81-88, 1999.
  • Majer BJ, Grummt T, Uhl M et al. Use of plant bioassays for the detection of genotoxins in aquatic environment. Acta Hydrochim Hydrobiol 33: 45-55, 2005.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
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