Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4246
Title: Evaluation of the genotoxicity and cytotoxicity of fexofenadine in cultured human peripheral blood lymphocytes
Authors: Kasurka, Ceren Borcek
Sekeroglu, Zulal Atli
Sekeroglu, Vedat
Ordu Üniversitesi
0000-0002-8547-6571
0000-0002-3552-3819
Keywords: Fexofenadine, Genotoxicity, Cytotoxicity, Chromosomal aberrations (CA), Micronucleus (MN)
IN-VITRO, MARKETED PHARMACEUTICALS, CHROMOSOME-ABERRATIONS, ANTIHISTAMINES, CARCINOGENICITY, IDENTIFICATION, TERFENADINE, POPULATION, ASTEMIZOLE, MANAGEMENT
Issue Date: 2011
Publisher: PERGAMON-ELSEVIER SCIENCE LTD-OXFORD
Citation: Kasurka, CB., Sekeroglu, ZA., Sekeroglu, V. (2011). Evaluation of the genotoxicity and cytotoxicity of fexofenadine in cultured human peripheral blood lymphocytes. Toxicol. Vitro, 25(7), 1480-1484. https://doi.org/10.1016/j.tiv.2011.05.002
Abstract: Fexofenadine (FXF) is a new non-sedating antihistamine used in the treatment of seasonal allergic rhinitis and chronic idiopathic urticaria. Studies on FXF genotoxicity and cytotoxicity in cultured human peripheral blood lymphocytes have not been reported so far. Therefore, the present study is the first report investigating the genotoxic and cytotoxic effects of FXF in cultured human peripheral blood lymphocytes in vitro. Cultures were treated with FXF at three concentrations (50, 100 and 150 mu g/ml) for 24 and 48 h. Endpoints analyzed included: mitotic index (MI), nuclear division index (NDI), chromosomal aberrations (CA) and micronucleus (MN) assay. Mitomycin C (MMC) was used as a positive control. The results of CA and MN assays showed that FXF was not genotoxic at all the concentrations tested, meanwhile MI and NDI results showed dose-dependent decrease and significant differences were found for at least one concentration. In conclusion, the results of this study suggest that FXF has a cytotoxic effect but not genotoxic effect on human peripheral blood lymphocyte cultures. Further cytogenetic studies, especially about the cell cycle kinetics of FXF are required to elucidate the decreases in dividing cells, and biomonitoring studies should also be conducted with patients receiving therapy with this drug. (C) 2011 Elsevier Ltd. All rights reserved.
Description: WoS Categories: Toxicology
Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED)
Research Areas: Toxicology
URI: http://dx.doi.org/10.1016/j.tiv.2011.05.002
https://www.webofscience.com/wos/woscc/full-record/WOS:000295066600029
http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4246
ISSN: 0887-2333
Appears in Collections:Moleküler Biyoloji ve Genetik Bölümü

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