Department of Toxicology "Akademik Danilo Soldatović", University of Belgrade - Faculty of Pharmacy, Vojvode Stepe 450, 11221, Belgrade, Serbia.
Department of Toxicology "Akademik Danilo Soldatović", University of Belgrade - Faculty of Pharmacy, Vojvode Stepe 450, 11221, Belgrade, Serbia.
Food Chem Toxicol. 2021 Dec;158:112671. doi: 10.1016/j.fct.2021.112671. Epub 2021 Nov 15.
The aim of this study was to explore the mechanisms of bis(2- ethylhexyl) phthalate (DEHP), dibutyl phthalate (DBP) and bisphenol A (BPA) mixture-induced asthma development and test probiotic as a potential positive intervention. Comparative Toxicogenomics Database (CTD) and ToppGene Suite were used as the main tools for in silico analysis. In vivo 28-day experiment was conducted on rats - seven groups (n = 6): (1) Control: corn oil, (2) P: probiotic (8.78 * 10 CFU/kg/day); (3) DEHP: 50 mg/kg b.w./day, (4) DBP: 50 mg/kg b.w./day, (5) BPA: 25 mg/kg b.w./day; (6) MIX: DEHP + DBP + BPA; (7) MIX + P. Lungs, thymus and kidneys were extracted and prepared for redox status and essential metals analysis. By conducting additional in vitro experiment, probiotic phthalate and BPA binding ability was explored. There were 24 DEHP, DBP and BPA asthma-related genes, indicating the three most probable mechanisms - apoptosis, inflammation and oxidative stress. In vivo experiment confirmed that significant changes in redox status/essential metal parameters were either prominent, or only present in the MIX group, indicating possible additive effects. In vitro experiment confirmed the ability of the multy-strain probiotic to bind DEHP/DBP/BPA mixture, while probiotic administration ameliorated mixture-induced changes in rat tissue.
本研究旨在探讨邻苯二甲酸二(2-乙基己基)酯(DEHP)、邻苯二甲酸二丁酯(DBP)和双酚 A(BPA)混合物诱导哮喘发展的机制,并测试益生菌作为一种潜在的积极干预措施。比较毒理学基因组数据库(CTD)和 ToppGene Suite 被用作计算机分析的主要工具。对大鼠进行了为期 28 天的体内实验,共分为七组(n=6):(1)对照组:玉米油,(2)P:益生菌(8.78*10 CFU/kg/天);(3)DEHP:50mg/kg b.w./天,(4)DBP:50mg/kg b.w./天,(5)BPA:25mg/kg b.w./天;(6)MIX:DEHP+DBP+BPA;(7)MIX+P。提取肺、胸腺和肾脏,并进行氧化还原状态和必需金属分析。通过进行额外的体外实验,探索了益生菌与邻苯二甲酸酯和 BPA 的结合能力。有 24 个与 DEHP、DBP 和 BPA 哮喘相关的基因,表明这三种最可能的机制 - 细胞凋亡、炎症和氧化应激。体内实验证实,氧化还原状态/必需金属参数的显著变化要么很明显,要么仅存在于 MIX 组中,表明可能存在相加作用。体外实验证实了多菌株益生菌结合 DEHP/DBP/BPA 混合物的能力,同时益生菌的给药改善了混合物对大鼠组织的诱导变化。