Laboratorio de Toxicología, Facultat de Farmàcia, Universitat de València, Av. Vicent Andres Estelles, s/n, 46117 Burjassot, Valencia, Spain.
Toxicol In Vitro. 2013 Mar;27(2):672-80. doi: 10.1016/j.tiv.2012.11.009. Epub 2012 Nov 17.
Enniatins (ENs) A, A1, B and B1 are produced by Fusarium species. They are known as emerging fusariotoxins, and can cause outbreaks in both humans and animals. ENs elicits a wide range of different biological properties and toxicological effects, and their co-occurrence may enhance the extent of these hazards. As the potential toxins reach in vitro cells in the same way as they would in vivo, cytotoxicity was studied with CHO-K1, which is considered one of the most sensitive cell lines for preliminary screening of cytotoxicity studies. In this study, individual cytotoxic effects of ENs were evaluated by MTT assay after exposing ENs to CHO-K1 cells for 24, 48, and 72h. The IC50 values obtained for ENs A, A1, B and B1 ranged from >7.5 to 2.83±0.49, from 8.8±2.29 to 1.65±0.06, from 11.0±2.65 to 2.80±0.16 and from 4.53±1.23 to 2.47±0.29μM, respectively. The ENs cytotoxic interaction was evaluated by the isobologram method. The IC50 values for ENs combination ranged from 0.44±0.15 (ENs A1+B1) to 0.97±0.48 (ENs A1+B+B1). The binary combinations ENs A+B1, ENs A1+B and ENs B+B1 showed additive effect thought all concentrations tested. Sinergistic effect of combined ENs A+A1, A+B, A1+B1, A+A1+B, A+A1+B1, A+B+B1 and A1+B+B1 at higher concentrations occurred. Synergism effect (CI from 0.37±0.08 to 0.74±0.22) was observed at higher concentrations with binary and tertiary combinations of EN A, while antagonism effect was obtained at lower concentrations for ENs A+A1+B1 (CI=2.67±1.32) and ENs A1+B+B1 (CI=3.14±1.91). These results provide quantitative evidence that ENs cytotoxicity depend on their concentrations, and also on their combination with other mycotoxins.
恩镰菌素(ENs)A、A1、B 和 B1 由镰刀菌属产生。它们被认为是新兴的镰刀菌毒素,会在人和动物中引发疾病。ENs 表现出广泛的不同生物学特性和毒理学效应,其共存可能会增强这些危害的程度。由于潜在毒素以与体内相同的方式到达体外细胞,因此使用 CHO-K1 细胞进行了细胞毒性研究,CHO-K1 被认为是细胞毒性研究初步筛选中最敏感的细胞系之一。在这项研究中,通过 MTT 测定法在暴露于 CHO-K1 细胞 24、48 和 72 小时后评估了 ENs 的单独细胞毒性效应。ENs A、A1、B 和 B1 的 IC50 值范围分别为>7.5 至 2.83±0.49、8.8±2.29 至 1.65±0.06、11.0±2.65 至 2.80±0.16 和 4.53±1.23 至 2.47±0.29μM。通过等辐射图方法评估了 ENs 的细胞毒性相互作用。ENs 组合的 IC50 值范围为 0.44±0.15(ENs A1+B1)至 0.97±0.48(ENs A1+B+B1)。在所有测试浓度下,ENs A+B1、ENs A1+B 和 ENs B+B1 的二元组合均表现出相加作用。在较高浓度下,组合的 ENs A+A1、A+B、A1+B1、A+A1+B、A+A1+B1、A+B+B1 和 A1+B+B1 显示出协同作用。在较高浓度下,ENs A 的二元和三元组合观察到协同作用(CI 为 0.37±0.08 至 0.74±0.22),而在较低浓度下,ENs A+A1+B1(CI=2.67±1.32)和 ENs A1+B+B1(CI=3.14±1.91)获得了拮抗作用。这些结果提供了定量证据,表明 ENs 的细胞毒性取决于其浓度,也取决于它们与其他霉菌毒素的组合。