| Literature DB >> 24355168 |
Wei Yang1, Miao Yu1, Juan Fu1, Wei Bao1, Di Wang1, Liping Hao1, Ping Yao1, Andreas K Nüssler2, Hong Yan3, Liegang Liu4.
Abstract
Deoxynivalenol (DON) is one of the most common mycotoxins. The aim of this study consists in using diverse cellular and molecular assays to evaluate cytotoxicity, genotoxicity as well as oxidative damage and to investigate their mechanisms in human peripheral blood lymphocytes. The human lymphocytes were cultured in eight different doses of DON (0, 6.25, 12.5, 25, 50, 100, 250 and 500 ng/mL) during 6, 12 and 24 h. DON was able to decrease cell viability and cause damage to the membrane, the chromosomes or the DNA at all times of culture. It was also able to induce lipid peroxidation and raise the levels of 8-OHdG and ROS in 6, 12 and 24 h. The results of the RT-PCR and the Western Blot indicated that DON is able to enhance mRNA or protein expressions of DNA repair genes and HO-1 in 6 h and to inhibit these expressions in 24 h. DON potentially triggers genotoxicity in human lymphocytes. This mechanism is probably related to depletion of antioxidase and oxidative damage to the DNA that reduced expression of HO-1, thereby inhibiting the ability of DNA repair.Entities:
Keywords: 2′, 7′-dichlorofluorescein; 5-methylcytosine; 8-OHdG; 8-hydroxydeoxyguanosine; BER; Cyt B; DCFH-DA; DNA repair; DON; Deoxynivalenol; GSH; GSSG; Genotoxicity; HO-1; HPLC; Hb; Human lymphocytes; L-glutathione oxidize; L-glutathione reduced; LC/MS; MDA, Lipid peroxidation; MMC; MN; Malonaldehyde; OECD; Organization for Economic Cooperation and Development; Oxidative damage; PHA; ROS; RT-PCR; SCE; X-ray repair cross-complementing protein-1; XRCC-1; base excision repair; cytochalasin B; deoxynivalenol; hOGG-1; heme oxygenase-1; hemoglobin; high-performance liquid chromatography; human oxoguanine glycosylase-1; liquid chromatography/mass spectrometry; m5dC; micronucleus cell; mitomycin C; phytohemagglutinin; reactive oxygen species; reverse transcription-polymerase chain reaction; sister chromatid exchange
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Year: 2013 PMID: 24355168 DOI: 10.1016/j.fct.2013.12.012
Source DB: PubMed Journal: Food Chem Toxicol ISSN: 0278-6915 Impact factor: 6.023