Tetrabromobisphenol A (TBBPA)-stimulated reactive oxygen species (ROS) production in cell-free model using the 2′,7′-dichlorodihydrofluorescein diacetate (H2DCFDA) assay-limitations of method

被引:60
作者
Szychowski, Konrad A. [1 ]
Rybczynska-Tkaczyk, Kamila [2 ]
Leja, Marcin L. [1 ]
Wojtowicz, Anna K. [3 ]
Gminski, Jan [1 ]
机构
[1] Univ Informat Technol & Management Rzeszow, Dept Publ Hlth Dietet & Lifestyle Disorders, Sucharskiego 2, PL-35225 Rzeszow, Poland
[2] Univ Life Sci, Dept Environm Microbiol, Lab Mycol, Leszczynskiego 7, PL-20069 Lublin, Poland
[3] Univ Agr, Dept Anim Biotechnol, Anim Sci Fac, Redzina 1B, PL-30248 Krakow, Poland
关键词
TBBPA; Free radical; H(2)DCFDA; DPPH; ROS; BROMINATED FLAME-RETARDANTS; FREE-RADICAL FORMATION; IN-VITRO; ANTIOXIDANT ACTIVITY; OXIDATIVE STRESS; NEUROTOXICITY; BIOLOGY;
D O I
10.1007/s11356-016-6450-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Tetrabromobisphenol A (TBBPA) is a widely used brominated flame retardant, applied in a variety of commercial and household products, mainly electronic ones. Since the production of reactive oxygen species (ROS) is considered one of the principal cytotoxicity mechanisms, numerous studies undertake that aspect of TBBPA's mechanism of action. The present study verifies if the fluorogenic substrate 2',7'-dichlorodihydrofluorescein diacetate (H(2)DCFDA) should be used to detect ROS production induced by TBBPA. To determine the ability of TBBPA alone to stimulate the conversion of H(2)DCFDA to its fluorescent product 2',7'-dichlorofluorescein (DCF), we used a cell-free model. In the experiments we check different cultured media also in combination with free radical scavenger N-acetyl-l-cysteine (NAC). Additionally, experiments with stable free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH center dot) have been made. The presented data showed that TBBPA in all tested concentrations interacts with H(2)DCFDA in phosphate-buffered saline (PBS) buffer while in micromolar concentrations in the DMEM/F12 medium with and without serum. The addition of NAC inhibited the interaction of TBBPA with H(2)DCFDA. Experiments with DPPH center dot showed that, in the presence of NAC, TBBPA acts like a free radical. TBBPA has similar properties to free radical and is susceptible to free radical scavenging properties of NAC. Our results indicated that H2DCFDA assay cannot be used to evaluate cellular ROS production in TBBPA studies. The study connected with TBBPA-stimulated ROS production in cell culture models using the H2DCFDA assay should be revised using a different method. However, due to the free radical-like nature of TBBPA, it can be very difficult. Therefore, further investigation of the nature of TBBPA as a compound with similar properties to free radical is required.
引用
收藏
页码:12246 / 12252
页数:7
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