Indicators of oxidative stress and apoptosis in mouse whole lung and Clara cells following exposure to styrene and its metabolites

• Published in: Toxicology (Amsterdam) 2009-10, Vol.264 (3), p.171-178
• Main Authors: Harvilchuck, Jill A, Pu, Xinzhu, Klaunig, James E, Carlson, Gary P
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Apoptosis - drug effects; bcl-2-Associated X Protein - genetics; bcl-2-Associated X Protein - metabolism; Biological and medical sciences; Biomarkers - metabolism; Carcinogens - administration & dosage; Carcinogens - metabolism; Carcinogens - toxicity; Caspase 3 - metabolism; Caspase 8 - metabolism; Cells, Cultured; Chemical and industrial products toxicology. Toxic occupational diseases; Clara cell; Deoxyguanosine - analogs & derivatives; Deoxyguanosine - metabolism; Emergency; Epithelial Cells - drug effects; Epithelial Cells - metabolism; Epithelial Cells - pathology; Epoxy Compounds - administration & dosage; Epoxy Compounds - metabolism; Epoxy Compounds - toxicity; Injections, Intraperitoneal; Lung - drug effects; Lung - metabolism; Lung - pathology; Male; Medical sciences; Mice; Oxidative stress; Oxidative Stress - drug effects; Proto-Oncogene Proteins c-bcl-2 - genetics; Proto-Oncogene Proteins c-bcl-2 - metabolism; Reactive Oxygen Species - metabolism; RNA, Messenger - metabolism; Solvents; Styrene; Styrene - administration & dosage; Styrene - metabolism; Styrene - toxicity; Styrene oxide; Superoxide Dismutase - metabolism; Time Factors; Toxicology
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/j.tox.2009.08.001

Abstract In mice, styrene is hepatotoxic, pneumotoxic, and causes lung tumors. One explanation for the mechanism of toxicity is oxidative stress/damage. Previous studies have shown decreased glutathione levels, linked to increased apoptosis, in lung homogenates and isolated Clara cells 3 h following styrene or styrene oxide (SO) administration or in vitro exposure. The objective of the current studies was to determine what effects styrene and its active metabolites, primarily styrene oxide, had on indicators of oxidative stress and attendant apoptosis in order to understand better the mechanism of styrene-induced toxicity. Three hours following in vitro exposure of Clara cells to styrene or SO there were increases in reactive oxygen species (ROS). Following administration of styrene or styrene oxide ip, increases in ROS, superoxide dismutase (SOD), and 8-hydroxydeoxyguanosine (8-OHdG) formation were observed. Since increases in ROS have been linked to increases in apoptosis ratios of bax/bcl-2, mRNA and protein expression were determined 3–240 h following the administration of styrene and R-styrene oxide (RSO). The bax/bcl-2 mRNA ratio increased 12 and 24 h following R-SO and 120 h following styrene administration. However, the bax/bcl-2 protein ratio was not increased until 240 h following R-SO, and 24 and 240 h following styrene administration. However, only a slight increase in caspase 3 was observed. These results indicated that oxidative stress occurred 3 h following styrene or styrene oxide as evidenced by increased ROS and SOD. This increased ROS may be responsible for the increased 8-OHdG formation. Our findings of limited apoptosis in Clara cells following acute exposure to styrene or SO are in agreement with others and may reflect the minimal extent to which apoptosis plays a role in acute styrene toxicity. It is clear, however, that oxidative stress and oxidative effects on DNA are increased following exposure to styrene or styrene oxide, and these may play a role in the lung tumorigenesis in mice.