The genoprotective activity of resveratrol on aflatoxin B-1-induced DNA damage in human lymphocytes in vitro

Turkez H., ŞİŞMAN T.

TOXICOLOGY AND INDUSTRIAL HEALTH, cilt.28, sa.5, ss.474-480, 2012 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 28 Sayı: 5
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1177/0748233711414614
  • Dergi Adı: TOXICOLOGY AND INDUSTRIAL HEALTH
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.474-480
  • Anahtar Kelimeler: Aflatoxin B-1, antigenotoxicity, human lymphocytes, resveratrol, sister chromatid exchanges, chromosome aberrations, SISTER-CHROMATID EXCHANGES, POTENTIAL CHEMOPROTECTIVE AGENT, SODIUM-CALCIUM ALUMINOSILICATE, WHOLE-BLOOD CULTURES, ANTIOXIDANT ACTIVITY, LIPID-PEROXIDATION, GENOTOXICITY, EXTRACTS, QUERCETIN, ACID
  • Atatürk Üniversitesi Adresli: Evet

Özet

Aflatoxin B-1 (AFB(1)) has been consistently shown to be a potent mutagen and carcinogen in humans and animals. On the other hand, resveratrol (RSV), a polyphenol, has several positive biological actions such as protection of cells against DNA damage. In the present study, the antigenotoxic effect of RSV was studied against a genotoxic dose of AFB(1) using the damage parameters of chromosomal aberrations (CAs) and sister chromatid exchanges (SCEs) in cultured human lymphocytes. Whole blood samples from three healthy male donors were used for this experiment and the effects of various concentrations of RSV (0, 10, 15, 25, 40, 75 and 100 mu M) and AFB(1) (10 mu M) were tested. The results revealed that the frequencies of SCEs and CAs in lymphocytes were significantly (p < 0.05) increased by AFB(1) as compared to controls. The results also showed that RSV was not genotoxic. Moreover, the number of SCEs and micronuclei induced by AFB(1) could be significantly minimized by the presence of RSV. Our results suggest for the first time that RSV can antagonize the ability of AFB(1) to cause DNA damage that leads to the formation of SCEs and CAs.