Effect of sulfur dioxide inhalation on the activities of glutathione peroxidase in nine organs of mice
Ziqiang Meng, Juli Bai
Abstract
Ziqiang Meng, Juli Bai
Abstract
In order to study oxidation damage of SO_(2) and mechanism of its toxicological role in mammals.After exposure to SO_(2) at different concentrations,the activities of glutathione peroxidase(GSH-Px) in nine-organs(liver,lung,kidney,heart,spleen,brain,stomach,small intestine and testicle0from mice were investigated.For male mice,the increases of GSH-Px activities were caused by SO_(2) at low concentration(22+-2mg/M_(3) in lungs(significant);while the decrease of GSH-Px activities were caused by low SO_(2) exposure in heart(significant) and in other organs(not significant).For female mice,SO_(2) at 22+-2mg.M_(3) caused increase of GSH-Px activities in all organs tested,but only the increase of GSH-Px activities in lungs and brains were statistically significant.SO_(2) at higher concentration(64+-3mg/M_(3) caused decrease of GSH-Px activities in all organs tested,but only the increase of GSH-POX activities in lungs and brains were statistically significant.SO_(2) at higher concentration(64+-3mg/M_(3)) caused decrease of GSH-Px activities in all organs tested in mice of both sexes,and the decrease of GSH-Px activities in liver,lung,kidney,heart,brain,stomach,intestine and testicle in male mice were statistically significant.SO_(2) might cause decrease of GSH-Px activities in various organs of mice in a dose-dependent manner.The decrease in activities of the antioxidant enzyme might predispose the organism to increase free radical dammage,and to reduce protection against lipid peroxidation.
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In order to study oxidation damage of SO_(2) and mechanism of its toxicological role in mammals.After exposure to SO_(2) at different concentrations,the activities of glutathione peroxidase(GSH-Px) in nine-organs(liver,lung,kidney,heart,spleen,brain,stomach,small intestine and testicle0from mice were investigated.For male mice,the increases of GSH-Px activities were caused by SO_(2) at low concentration(22+-2mg/M_(3) in lungs(significant);while the decrease of GSH-Px activities were caused by low SO_(2) exposure in heart(significant) and in other organs(not significant).For female mice,SO_(2) at 22+-2mg.M_(3) caused increase of GSH-Px activities in all organs tested,but only the increase of GSH-Px activities in lungs and brains were statistically significant.SO_(2) at higher concentration(64+-3mg/M_(3) caused decrease of GSH-Px activities in all organs tested,but only the increase of GSH-POX activities in lungs and brains were statistically significant.SO_(2) at higher concentration(64+-3mg/M_(3)) caused decrease of GSH-Px activities in all organs tested in mice of both sexes,and the decrease of GSH-Px activities in liver,lung,kidney,heart,brain,stomach,intestine and testicle in male mice were statistically significant.SO_(2) might cause decrease of GSH-Px activities in various organs of mice in a dose-dependent manner.The decrease in activities of the antioxidant enzyme might predispose the organism to increase free radical dammage,and to reduce protection against lipid peroxidation.
Key concepts: Glutathione, Glutathione peroxidase, Kidney, Lipid peroxidation, Internal medicine, Endocrinology, Lung, Spleen