Please use this identifier to cite or link to this item: 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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