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dc.contributor.authorERDOĞMUŞ, SEVİM FEYZA
dc.contributor.authorDAĞOĞLU SAKİN, Rabia Nergiz
dc.contributor.authorÖZKARA, ARZU
dc.contributor.authorAKYIL, DİLEK
dc.contributor.authorEren, Yasin
dc.contributor.authorKONUK, MUHSİN
dc.date.accessioned2022-02-18T10:20:06Z
dc.date.available2022-02-18T10:20:06Z
dc.date.issued2015
dc.identifier.citationÖZKARA A., AKYIL D., Eren Y., ERDOĞMUŞ S. F. , KONUK M., DAĞOĞLU SAKİN R. N. , "Assessment of cytotoxic and genotoxic potential of pyracarbolid by Allium test and micronucleus assay", DRUG AND CHEMICAL TOXICOLOGY, cilt.38, sa.3, ss.337-341, 2015
dc.identifier.issn0148-0545
dc.identifier.otherav_9220eda2-a58f-4895-8157-179793222612
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/179039
dc.identifier.urihttps://doi.org/10.3109/01480545.2014.966831
dc.description.abstractThe present study evaluates the cytotoxic and genotoxic potential of pyracarbolid using both micronuleus (MN) assay, in human lymphocytes, and Allium cepa assay, in the root meristem cells. In Allium test, EC50 value was determined in order to selecting the test concentrations for the assay and the root tips were treated with 25 ppm (EC50/2), 50 ppm (EC50) and 100 ppm (EC50 x 2) concentrations of pyracarbolid. One percent of dimethyl sulphoxide (DMSO) and methyl methane sulfonate (MMS) were used as negative and positive controls, respectively. In the micronucleus assay, the cultures were treated with four concentrations (250, 500, 750 and 1000 mu g/ml) of pyracarbolid for 24 and 48 h, negative and positive controls were also used in the experiment parallely. The results showed that mitotic index (MI) significantly reduced with increasing the pyracarbolid concentration at each exposure time. It was also obtained that prophase and metaphase index decreased significantly in all concentration at each exposure time. Anaphase index decreased as well and results were found to be statistically significant, except 24 h. A significant increase was observed in MN frequency in all concentrations and both treatment periods when compared with the controls. Pyracarbolid also caused a significant reduction in the cytokinesis block proliferation index (CBPI) in all concentration and both exposure time.
dc.language.isoeng
dc.subjectHealth Sciences
dc.subjectPharmacology, Toxicology and Pharmaceutics (miscellaneous)
dc.subjectHealth, Toxicology and Mutagenesis
dc.subjectChemistry (miscellaneous)
dc.subjectGeneral Chemistry
dc.subjectPharmacology (medical)
dc.subjectPharmacy
dc.subjectDrug Guides
dc.subjectPhysical Sciences
dc.subjectLife Sciences
dc.subjectKİMYA, MULTİDİSİPLİNER
dc.subjectKimya
dc.subjectTemel Bilimler (SCI)
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTOKSİKOLOJİ
dc.subjectSağlık Bilimleri
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectMeslek Bilimleri
dc.subjectFarmasötik Toksikoloji
dc.subjectYaşam Bilimleri
dc.subjectBiyokimya
dc.subjectAlkoloidler
dc.subjectTemel Bilimler
dc.subjectToxicology
dc.subjectPharmacology
dc.subjectGeneral Pharmacology, Toxicology and Pharmaceutics
dc.titleAssessment of cytotoxic and genotoxic potential of pyracarbolid by Allium test and micronucleus assay
dc.typeMakale
dc.relation.journalDRUG AND CHEMICAL TOXICOLOGY
dc.contributor.departmentAfyon Kocatepe Üniversitesi , ,
dc.identifier.volume38
dc.identifier.issue3
dc.identifier.startpage337
dc.identifier.endpage341
dc.contributor.firstauthorID3382875


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