Protective effects of selenium against sister chromatid exchange induced by AFG(1) in human lymphocytes in vitro

Alpsoy L., KOTAN E., TATAR A., AĞAR G.

HUMAN & EXPERIMENTAL TOXICOLOGY, cilt.30, sa.6, ss.515-519, 2011 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 30 Sayı: 6
  • Basım Tarihi: 2011
  • Doi Numarası: 10.1177/0960327110377523
  • Dergi Adı: HUMAN & EXPERIMENTAL TOXICOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.515-519
  • Anahtar Kelimeler: Aflatoxin G(1), genotoxicity, sister chromatid exchange, selenium, CULTURED HUMAN-LYMPHOCYTES, CHROMOSOME-ABERRATIONS, BLOOD LYMPHOCYTES, DIETARY SELENIUM, VITAMIN-E, COVALENT BINDING, AFLATOXIN B-1, CROP PLANTS, DNA-DAMAGE, CELLS
  • Atatürk Üniversitesi Adresli: Evet

Özet

Aflatoxins have been shown to be hepatotoxic, carcinogenic, mutagenic and teratogenic to different species of animals. Besides, at low concentrations, Selenium (Se4+) is antimutagenic and anticarcinogenic while it is toxic, mutagenic and carcinogenic at high concentrations. In this study, we aimed to evaluate the effect of Se4+ against aflatoxin GAFG(1) (AFG(1)) on blood cultures in relation to induction of sister chromatid exchange (SCE). The results showed that at 0.4 and 0.8 parts per million (ppm) concentration of AFG(1), the frequency of SCE increased in cultured human lymphocytes. When different concentration of Se4+ (0.08 and 8 ppm) were added to AFG(1), the frequencies of SCE decreased. Howewer, when 800 ppm concentration of Se4+ together with 0.08 ppm AFG(1) were added to cell division inhibited in the cultures. Results suggested that Se4+ could effectively inhibit AFG(1)-induced SCE. Besides, the protective role of Se4+ against AFG(1)-induced SCE is probably related to its doses.