Research Group in Alternative Methods for Determining Toxics Effects and Risk Assessment of Contaminants and Mixtures (RiskTox), Spain; Laboratory of Toxicology, Faculty of Pharmacy, University of Valencia, Av. Vicent Andrés Estellés s/n, 46100, Valencia, Spain; Department of Industrial Engineering (DII), University of Padua, Via Marzolo 9, 35131, Padova, Italy; Fondazione Istituto di Ricerca Pediatrica Cittá Della Speranza (IRP)-Lab BIAMET, Corso Stati Uniti 4, 35127, Padova, Italy.
Department of Industrial Engineering (DII), University of Padua, Via Marzolo 9, 35131, Padova, Italy; Fondazione Istituto di Ricerca Pediatrica Cittá Della Speranza (IRP)-Lab BIAMET, Corso Stati Uniti 4, 35127, Padova, Italy.
Food Chem Toxicol. 2024 Oct;192:114951. doi: 10.1016/j.fct.2024.114951. Epub 2024 Aug 23.
Humans are exposed to complex mixtures of mycotoxins through diet. Despite the serious threat they pose, mycotoxin risk assessment often overlooks co-exposure. With the aim of filling this gap, the present study investigates the combined cytotoxicity of sterigmatocystin (STE), ochratoxin A (OTA) and patulin (PAT) in human tumour Neuroblastoma and healthy Mesenchymal Stem Cells three-dimensional (3D) spheroids. The range of concentrations tested (1.56-50 μM for STE, 0.78-25 μM for OTA and 0.15-5 μM for PAT) was selected considering the IC values obtained in previous studies and the estimated dietary exposure of consumers. To ensure appropriate experimental conditions, assessments for single mycotoxins and their combinations were conducted simultaneously. The nature of the toxicological interactions among the mycotoxins was then defined using the isobologram analysis. Our results demonstrated increased cytotoxicity in mycotoxin mixtures compared to individual exposure, with abundance of synergistic interactions. These findings highlight that the co-occurrence of STE, OTA and PAT in food may increase their individual toxic effects and should not be underestimated. Moreover, the use of advanced culture models increased the reliability and physiological relevance of our results which can serve as a groundwork for formulating standardized regulatory approaches towards mycotoxin mixtures in food and feed.
人类通过饮食暴露于复杂的霉菌毒素混合物中。尽管它们构成了严重的威胁,但霉菌毒素风险评估往往忽略了共同暴露。有鉴于此,本研究调查了在人类肿瘤神经母细胞瘤和健康间充质干细胞三维(3D)球体中,赭曲霉毒素 A(OTA)和展青霉素(PAT)的组合细胞毒性。考虑到先前研究中获得的 IC 值和消费者估计的饮食暴露量,选择了测试的浓度范围(STE 为 1.56-50 μM,OTA 为 0.78-25 μM,PAT 为 0.15-5 μM)。为确保适当的实验条件,同时进行了单一霉菌毒素及其组合的评估。然后使用等辐射图分析来定义霉菌毒素之间毒理学相互作用的性质。我们的结果表明,与单独暴露相比,霉菌毒素混合物的细胞毒性增加,存在丰富的协同相互作用。这些发现强调了食品中 STE、OTA 和 PAT 的共同存在可能会增加它们各自的毒性作用,不应被低估。此外,先进培养模型的使用提高了我们研究结果的可靠性和生理相关性,可为制定食品和饲料中霉菌毒素混合物的标准化监管方法奠定基础。