Continuous hypoxia attenuates paraquat-induced cytotoxicity in the human A549 lung carcinoma cell line.
10.3858/emm.2011.43.9.056
- Author:
Hoon KIM
1
;
Suk Woo LEE
;
Kyung Min BAEK
;
Jung Soo PARK
;
Jin Hong MIN
Author Information
1. Department of Emergency Medicine, Chungbuk National University College of Medicine, Cheongju 361-763, Korea. nichekh2000@chungbuk.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
cell death;
hypoxia;
oxidative stress;
paraquat;
reactive oxygen species
- MeSH:
Apoptosis/drug effects;
Cell Line, Tumor;
Cell Proliferation/drug effects;
Flavonoids/pharmacology;
*Gene Expression Regulation, Neoplastic;
Hepatocyte Growth Factor/*pharmacology;
Humans;
Inhibitor of Apoptosis Proteins/antagonists & inhibitors/*genetics;
MAP Kinase Kinase Kinases/antagonists & inhibitors;
Neoplasm Invasiveness;
Promoter Regions, Genetic;
Protein Binding;
Proto-Oncogene Proteins c-jun/genetics/*metabolism;
Stomach Neoplasms/genetics/*metabolism/pathology;
Urokinase-Type Plasminogen Activator/*genetics
- From:Experimental & Molecular Medicine
2011;43(9):494-500
- CountryRepublic of Korea
- Language:English
-
Abstract:
Paraquat (1,1'-dimethyl-4,4'-bipyridinium dichloride; PQ), an effective and widely used herbicide, was commercially introduced in 1962. It is reduced by the electron donor NADPH, and then reduced PQ transfers the electrons to molecular oxygen, resulting in the production of reactive oxygen species (ROS), which are related to cellular toxicity. However, the influence of continuous hypoxia on PQ-induced ROS production has not fully been investigated. We evaluated in vitro the protective effect of continuous hypoxia on PQ-induced cytotoxicity in the human carcinogenic alveolar basal epithelial cell line (A549 cells) by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay and live and dead assay, and by measuring lactate dehydrogenase (LDH) release. To elucidate the mechanism underlying this effect, we monitored the immunofluorescence of intracellular ROS and measured malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GPx) activities. Continuous hypoxia protected the A549 cells from PQ-induced cytotoxicity. Continuous hypoxia for a period of 24 h significantly reduced intracellular ROS, decreased MDA concentration in the supernatant, and normalized SOD and GPx activities. Continuous hypoxia attenuated PQ-induced cell toxicity in A549 cells. This protective effect might be attributable to the suppression of PQ-induced ROS generation.
