dc.contributor.author | Avuloglu-Yilmaz E. | |
dc.contributor.author | Yuzbasioglu D. | |
dc.contributor.author | Unal F. | |
dc.date.accessioned | 2024-03-12T19:35:20Z | |
dc.date.available | 2024-03-12T19:35:20Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 01480545 | |
dc.identifier.uri | https://doi.org/10.1080/01480545.2022.2026375 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12450/2889 | |
dc.description.abstract | Hypertension is the most common cardiovascular disease and is also known as high blood pressure. The large majority of hypertensive patients need long-term administration of antihypertensive agents. Indapamide is an orally administered diuretic antihypertensive drug. The present work aimed to assess the possible genotoxic effects of indapamide using four different assays: chromosomal aberration (CA), sister chromatid exchange (SCE), micronucleus (MN), and comet. Lymphocytes from three different donors were exposed to 18.75, 37.50, 75.00, and 100.00 ?g/ml indapamide. Additionally, a negative, a positive (mitomycin C = MMC, 0.20 ?g/ml), and a solvent control (5.4 ?l/ml methanol) were also applied. As a result, it was seen that indapamide did not cause a significant change in CAs and MN frequencies compared to the control. It caused significant damage only at the highest concentration in the comet assay. Similarly, while it did not affect the number of SCEs in the 24-h treatment, it increased the SCE frequency at the two highest concentrations in the 48-h. Mitotic index (MI) decreased at almost all concentrations. Considering all these results, this study revealed that indapamide did not have a significant genotoxic effect in these conditions. To the best of our knowledge, this is the first investigation about the genotoxic effect of indapamide in human lymphocytes in vitro. © 2022 Informa UK Limited, trading as Taylor & Francis Group. | en_US |
dc.description.sponsorship | 05/2015–16 | en_US |
dc.description.sponsorship | This work was supported by the Gazi University Research Fund under Grant number 05/2015–16. Graphical abstract was created using BioRender App. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Taylor and Francis Ltd. | en_US |
dc.relation.ispartof | Drug and Chemical Toxicology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | an antihypertensive drug | en_US |
dc.subject | genotoxicity | en_US |
dc.subject | human lymphocytes | en_US |
dc.subject | Indapamide | en_US |
dc.subject | the active ingredient | en_US |
dc.subject | indapamide | en_US |
dc.subject | methanol | en_US |
dc.subject | mitomycin | en_US |
dc.subject | solvent | en_US |
dc.subject | antihypertensive agent | en_US |
dc.subject | indapamide | en_US |
dc.subject | adult | en_US |
dc.subject | Article | en_US |
dc.subject | chromosome aberration | en_US |
dc.subject | comet assay | en_US |
dc.subject | controlled study | en_US |
dc.subject | female | en_US |
dc.subject | genotoxicity | en_US |
dc.subject | human | en_US |
dc.subject | human cell | en_US |
dc.subject | in vitro study | en_US |
dc.subject | lymphocyte | en_US |
dc.subject | male | en_US |
dc.subject | micronucleus | en_US |
dc.subject | mitosis index | en_US |
dc.subject | sister chromatid exchange | en_US |
dc.subject | DNA damage | en_US |
dc.subject | lymphocyte | en_US |
dc.subject | micronucleus test | en_US |
dc.subject | Antihypertensive Agents | en_US |
dc.subject | DNA Damage | en_US |
dc.subject | Humans | en_US |
dc.subject | Indapamide | en_US |
dc.subject | Lymphocytes | en_US |
dc.subject | Micronucleus Tests | en_US |
dc.subject | Mitomycin | en_US |
dc.title | Assessment of the genotoxic effects of antihypertensive drug active ingredient indapamide in human lymphocytes | en_US |
dc.type | article | en_US |
dc.department | Amasya Üniversitesi | en_US |
dc.identifier.volume | 46 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.startpage | 297 | en_US |
dc.identifier.endpage | 303 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopus | 2-s2.0-85122820821 | en_US |
dc.identifier.doi | 10.1080/01480545.2022.2026375 | |
dc.department-temp | Avuloglu-Yilmaz, E., Vocational School of Technical Sciences, Amasya University, Amasya, Turkey; Yuzbasioglu, D., Department of Biology, Faculty of Science, Genetic Toxicology Laboratory, Gazi University, Ankara, Turkey; Unal, F., Department of Biology, Faculty of Science, Genetic Toxicology Laboratory, Gazi University, Ankara, Turkey | en_US |
dc.authorscopusid | 57189069248 | |
dc.authorscopusid | 6506526163 | |
dc.authorscopusid | 7004407682 | |
dc.identifier.pmid | 35016574 | en_US |