Mohmood Iram, Ahmad Iqbal, Asim Mohammad, Costa Leonor, Lopes Cláudia B, Trindade Tito, Duarte Armando C, Pereira Eduarda
Department of Chemistry & CESAM, University of Aveiro, 3810-193, Aveiro, Portugal.
Environ Sci Pollut Res Int. 2015 Mar;22(5):3687-96. doi: 10.1007/s11356-014-3591-3. Epub 2014 Sep 27.
The study aimed to assess the genotoxic potential of silica-coated iron oxide nanoparticle functionalized with dithiocarbamate groups (IONP, 100 nm) in vitro exposure alone or its interference with mercury (Hg) co-exposure in the blood of European eel (Anguilla anguilla L.) by evaluating 8-hydroxy-2'-deoxyguanosine (8-OHdG), lipid peroxidation (LPO), and erythrocytic nuclear abnormalities (ENA). Four groups were made: (i) 2 × 10(6) erythrocytes + Roswell Park Memorial Institute-1640 (RPMI-1640) (control), (ii) 2 × 10(6) erythrocytes + IONP (2.5 mg L(-1)), (iii) 2 × 10(6) erythrocytes + Hg (50 μg L(-1)), and (iv) 2 × 10(6) erythrocytes + IONP + Hg. Blood plasma was also processed following the previous exposure conditions. Samplings were performed at 0, 2, 4, 8, 16, 24, 48, and 72 h of exposure. The results revealed significant ENA increases at both early (2, 4, 8) and late (16, 24, 48, 72) hours of exposure to IONP alone. However, IONP exposure combined with Hg co-exposure revealed no ENA increase at 2 h, suggesting that IONP-Hg complex formation is efficient to eliminate the DNA damage induced by individual exposure to IONP or Hg at early hours. Hence, the initial occurrence of antagonism between IONP and Hg was perceptible; however, at late hours of exposure, IONP was unable to mitigate the mercury-accrued negative impacts. Plasma exposure to IONP alone displayed a significant increase in 8-OHdG levels at 2 and 48 h of exposure. However, IONP in combination with Hg co-exposure revealed an increase in 8-OHdG levels at all the exposure length (except 16 h), suggesting that both IONP and Hg independently oxidized DNA. In addition, an additive effect on 8-OHdG levels at both early and late hours, and on LPO only at late hours (except 24 h), suggested that DNA is more susceptible to peroxidative damage than lipid.
该研究旨在通过评估8-羟基-2'-脱氧鸟苷(8-OHdG)、脂质过氧化(LPO)和红细胞核异常(ENA),来评估二硫代氨基甲酸盐基团功能化的二氧化硅包覆氧化铁纳米颗粒(IONP,100纳米)单独体外暴露的遗传毒性潜力,以及其对欧洲鳗鲡(Anguilla anguilla L.)血液中汞(Hg)共同暴露的干扰作用。实验分为四组:(i)2×10⁶个红细胞+罗斯韦尔公园纪念研究所-1640培养基(RPMI-1640)(对照组),(ii)2×10⁶个红细胞+IONP(2.5毫克/升),(iii)2×10⁶个红细胞+Hg(50微克/升),以及(iv)2×10⁶个红细胞+IONP+Hg。血浆也按照先前的暴露条件进行处理。在暴露的0、2、4、8、16、24、48和72小时进行采样。结果显示,单独暴露于IONP时,在早期(2、4、8小时)和晚期(16、24、48、72小时)ENA均显著增加。然而,IONP暴露与Hg共同暴露相结合时,在2小时时ENA没有增加,这表明IONP-Hg复合物的形成有效地消除了早期单独暴露于IONP或Hg所诱导的DNA损伤。因此,IONP和Hg之间最初的拮抗作用是明显的;然而,在暴露后期,IONP无法减轻汞积累的负面影响。单独暴露于IONP的血浆在暴露2小时和48小时时8-OHdG水平显著增加。然而,IONP与Hg共同暴露时,在所有暴露时长(除16小时外)8-OHdG水平均增加,这表明IONP和Hg均可独立氧化DNA。此外,在早期和晚期对8-OHdG水平以及仅在晚期(除24小时外)对LPO有相加作用,这表明DNA比脂质更容易受到过氧化损伤。