Yayın: In vitro antigenotoxicity of ulva rigida c. agardh (chlorophyceae) extract against induction of chromosome aberration, sister chromatid exchange and micronuclei by mutagenic agent MMC
Tarih
Kurum Yazarları
Çelikler, Serap
Yıldız, Gamze
Vatan, Özgür
Bilaloǧlu, Rahmi
Yazarlar
Danışman
Dil
Türü
Yayıncı:
Chinese Center Disaese Control & Prevention
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Özet
Objective To determine the in vitro possible clastogenic and cytotoxic activities of Ova rigida crude extracts (URE), and identify their antigenotoxic and protective effects on chemotherapeutic agent mitomycine-C (MMC). Methods Anti-clastogenic and anti-genotoxic activities of Ulva rigida crude extracts (URE) were studied using chromosome aberration (CA), sister chromatid exchange (SCE), and micronuclei (MN) tests in human lymphocytes cultured in vitro. Results The chromosome aberration, sister chromatid exchange or micronuclei tests showed that URE at concentrations of 10, 20, and 40 mu g/mL had no clastogenic activity in human lymphocyte cell Culture. Three doses of URE significantly decreased the number of chromosomal aberrations and the frequencies of SCE and MN when compared with the culture treated with MMC (P<0.0001). Conclusion Although URE itself is not a clastogenic or cytotoxic substance, it possesses strong antigenotoxic, anti-clastogenic, and protective effects on MMC in vitro.
Açıklama
Kaynak:
Anahtar Kelimeler:
Konusu
Chlorophyceae, Ulva, Ulva rigida, Chromosomal aberration, Antigenotoxicity, Anticlastogenicity, Micronuclei, Mitomycin-C, Sister chromatid exchange, Ulva rigida, Wakame undaria-pinnatifida, Antibacterial activity, Marine-algae, Natural-products, Seaweed, Cells, Purification, Antioxidants, Carotenoids, Carcinoma, Environmental sciences & ecology, Public, environmental & occupational health
Alıntı
Çelikler, S. vd. (2008). ''In vitro antigenotoxicity of ulva rigida c. agardh (chlorophyceae) extract against induction of chromosome aberration, sister chromatid exchange and micronuclei by mutagenic agent MMC''. Biomedical and Environmental Sciences, 21(6), 492-498.
