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https://hdl.handle.net/11499/9821
Title: | Delineating the antigenotoxic and anticytotoxic potentials of 4-methylimidazole against ethyl methanesulfonate toxicity in bone marrow cell of swiss albino mice | Authors: | Norizadeh Tazehkand, M. Topaktas, M. Yilmaz, M.B. Hajipour ?Orkideh Valipour, E. |
Keywords: | Anticytotoxicity Antigenotoxicity Chromosome aberration Ethyl methansulfonate Methylimidazole 4-methylimidazole imidazole derivative mesylic acid ethyl ester mutagenic agent animal bone marrow cell cell proliferation chromosome aberration DNA damage drug effects female male mitosis index mouse Animals Bone Marrow Cells Cell Proliferation Chromosome Aberrations DNA Damage Ethyl Methanesulfonate Female Imidazoles Male Mice Mitotic Index Mutagens |
Publisher: | Comenius University | Abstract: | 4-Methylimidazole (4-MEI) is mostly used in beverages and coloring food, dark beers and common brands of cola drinks, which may contain more than 100 µg of this compound per 12-ounce serving. This study was aimed to investigate the antigenotoxic and anticytotoxic effects of 4-MEI (100, 130 and 160 mg/kg) against ethyl methanesulfonate (240 mg/kg) using chromosome aberrations (CAs) and Mitotic index (MI) tests in bone marrow cells of Swiss Albino Mice at 12 h and 24 h treatment periods. So, the t-test was used for the statistical analysis. In this research, 4-MEI at all concentrations for 12 h treatment period reduced chromosomal aberrations and at 130 and 160 mg/kg concentrations for 24 h treatment period increased chromosomal aberrations induced by EMS (240 mg/kg), but th ese reductions and increases were not significant. Also, intraperitoneal injection of 4-MEI at doses of 100, 130 and 160 mg/kg combined with EMS (240 mg/kg) showed that the mitotic index was decreased at 100 and 130 mg/kg for 12h and 130 mg/kg for 24 h treatment periods, when compared to positive sample (EMS), but did not show any statistically difference from the EMS treated group. It can be concluded that 4-MEI might not be antigenotoxic and protective effects in bone marrow cells of Swiss Albino Mice, because 4-MEI could not reduce the chromosomal aberrations induced by EMS. | URI: | https://hdl.handle.net/11499/9821 https://doi.org/10.4149/BLL_2016_057 |
ISSN: | 0006-9248 |
Appears in Collections: | Fen-Edebiyat Fakültesi Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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Hajipour, O.pdf | 205.04 kB | Adobe PDF | View/Open |
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