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Updated: Jun 27, 2026

Imaging Approaches to Assessments of Toxicological Oxidative Stress Using Genetically-encoded Fluorogenic Sensors
Published on: February 7, 2018
[Cytotoxicity induced by gasoline engine exhausts associated with oxidative stress]
Wangjun Che1, Zunzhen Zhang, Mei Wu
1West China School of Public Health, Sichuan University, Chengdu 610041, China.
Objective:
To evaluate the relationship between cytotoxic effects of the extracts of condensate, particulates and semivolatile organic compounds from gasoline engine exhausts (EGE) and oxidative stress.
Methods:
After A549 cells were treated with various concentrations of EGE for 2h, and cell viabilities were detected induced by EGE were examined by MTT assay. Meanwhile, the reactive oxygen species (ROS) in A549 cells induced by EGE were examined, 2',7'-dichlorodihy-drofluorescin diacetate (DCFH-DA) was used to catch ROS and its level measured by value of pixel fluorescence intensity. Furthermore, A549 cells pretreated with different concentrations of glutathione (GSH) were exposed to various concentrations of EGE for 2h, and then cell viabilities were examined.
Results:
Viabilities of A549 cells significantly decreased in comparison to the solvent group when the concentrations of EGE were more than 3.9 ml/ml (P < 0.05). There were a dose-response relationships between the viabilities and the concentration of EGE (r = -0.81, P < 0.01). At the concentrations of 31.3 ml/ml and 62.5 ml/ml, the values of pixel fluorescence intensity were (125.0 +/- 19.2) and (168.9 +/- 16.9), which were significantly higher than those of control (8.5 +/- 1.4). In addition, the viabilities of cells pretreated with GSH gradually increased with the increases of the concentrations of GSH. There were also a significant difference between the pretreated and non-pretreated group at the concentrations of 0.5 mmol/L and 1.0 mmol/L.
Conclusion:
Oxidative stress could be one of the mechanisms of cytotoxic effects of EGE.
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