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dc.contributor.authorBecerir, Hatice Bilge
dc.contributor.authorBagatir, Gulcin
dc.contributor.authorKaya, Murat
dc.contributor.authorSuer, İlknur
dc.contributor.authorÇefle, Kıvanç
dc.contributor.authorPalanduz, Ayşe
dc.contributor.authorPalanduz, Şükrü
dc.contributor.authorÖztürk, Şükrü
dc.contributor.authorKoçyiğit Avcı, Mine
dc.date.accessioned2022-07-04T15:53:22Z
dc.date.available2022-07-04T15:53:22Z
dc.identifier.citationBagatir G., Kaya M., Suer İ., Çefle K., Palanduz A., Palanduz Ş., Becerir H. B. , Koçyiğit Avcı M., Öztürk Ş., "The effect of Anzer honey on X-ray induced genotoxicity in human lymphocytes: An in vitro study", MICROSCOPY RESEARCH AND TECHNIQUE, 2022
dc.identifier.issn1059-910X
dc.identifier.othervv_1032021
dc.identifier.otherav_c7f0ebfd-6673-4863-8160-58ea823af64f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/184643
dc.identifier.urihttps://doi.org/10.1002/jemt.24081
dc.description.abstractAnzer honey is well known in Turkey and used for its medicinal properties, especially for pharyngitis, tonsillitis, ulcers and cancer. In this study, we investigated whether Anzer honey, which is shown to have antioxidant, anti-tumoral, and anti-inflammatory properties, has a protective effect against X-ray induced genotoxic damage by cytogenetic methods. Peripheral blood lymphocytes isolated from 20 healthy volunteers were divided into two groups and cultivated by conventional methods. Study group lymphocytes were treated with 10% diluted honey while those in the control group were not. Both groups were exposed to a high dose (2 Gy) X-ray at the 48th hour of culture. Conventional cytogenetic staining and Giemsa banding methods were applied to evaluate chromosomal breakage and ring formation. Micronucleus frequencies were determined by the cytokinesis-block micronucleus (CBMN) assay. Paired sample t test was used to compare groups. Anzer honey, which was analyzed melissopalynologically, was used. Micronucleus frequency was significantly decreased in the study group (CI = 348.75 +/- 31, median 326, min. 98, max. 704) compared to the control group (CI = 489.10 +/- 27, median 500, min. 216, max. 645) (p = .001). Chromosomal breakage was also significantly decreased in the study group (CI = 118.70 +/- 16, median 109, min. 12, max. 316) compared to the control group (CI = 233.60 +/- 25, median 225, min. 65, max. 492) (p < .0001). This is the first study indicating that genotoxic damage in the peripheral blood lymphocytes of healthy volunteers induced by X-radiation may be prevented or alleviated by adding Anzer honey in vitro. These results encourage further research about the protective effects of honey.
dc.language.isoeng
dc.subjectBiochemistry (medical)
dc.subjectANATOMİ VE MORFOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBİYOLOJİ
dc.subjectMİKROSKOPİ
dc.subjectMikrobiyoloji
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectAnatomi
dc.subjectBiyokimya
dc.subjectTıbbi Biyoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectAnatomy
dc.subjectHealth Sciences
dc.titleThe effect of Anzer honey on X-ray induced genotoxicity in human lymphocytes: An in vitro study
dc.typeMakale
dc.relation.journalMICROSCOPY RESEARCH AND TECHNIQUE
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.contributor.firstauthorID3394347


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