Potassium bromate causes cell lysis and induces oxidative stress in human erythrocytes
Authors:
- 19 October 2011
- journal article
- research article
- Published by Wiley in Environmental Toxicology
- Vol. 29 (2) , 138-145
Abstract
In the present study, we have studied the effect of KBrO3 on human erythrocytes under in vitro conditions. Erythrocytes were isolated from the blood of healthy nonsmoking volunteers and incubated with different concentrations of KBrO3 at 37°C for 60 min. This resulted in marked hemolysis in a KBrO3-concentration dependent manner. Lysates were prepared from KBrO3-treated and control erythrocytes and assayed for various parameters. KBrO3 treatment caused significant increase in protein oxidation, lipid peroxidation, hydrogen peroxide levels, and decrease in total sulfhydryl content, which indicates induction of oxidative stress in human erythrocytes. Methemoglobin levels and methemoglobin reductase activity were significantly increased while the total antioxidant power of lysates was greatly reduced upon KBrO3 treatment. Intracellular production of reactive oxygen species increased in a dose dependent manner. Exposure of erythrocytes to KBrO3 also caused decrease in the activities of catalase, glutathione peroxidase, thioredoxin reductase, glucose 6-phosphate dehydrogenase and glutathione reductase whereas the activities of Cu-Zn superoxide dismutase and glutathione-S-transferase were increased. These results show that KBrO3 induces oxidative stress in human erythrocytes through the generation of reactive oxygen species and alters the cellular antioxidant defense system. © 2011 Wiley Periodicals, Inc. Environ Toxicol 29: 138–145, 2014.Keywords
This publication has 46 references indexed in Scilit:
- Possible involvement of oxidative stress in potassium bromate-induced genotoxicity in human HepG2 cellsChemico-Biological Interactions, 2011
- Early alterations in protein and gene expression in rat kidney following bromate exposureFood and Chemical Toxicology, 2009
- The multiple influences of glutathione on bromate genotoxicity: Implications for the dose–response relationshipToxicology, 2006
- Protective effects of melatonin and indole‐3‐propionic acid against lipid peroxidation, caused by potassium bromate in the rat kidneyCell Biochemistry and Function, 2006
- Abrogation of potassium bromate-induced renal oxidative stress and subsequent cell proliferation response by soy isoflavones in Wistar ratsToxicology, 2004
- Kolaviron Modulates cellular redox status and impairment of membrane protein activities induced by potassium bromate (KBrO3) in ratsPharmacological Research, 2002
- Oxidative DNA damage induced by potassium bromate in isolated rat renal proximal tubules and renal nucleiCancer Letters, 1994
- Relation of 8‐Hydroxydeoxyguanosine Formation in Rat Kidney to Lipid Peroxidation, Glutathione Level and Relative Organ Weight after a Single Administration of Potassium BromateJapanese Journal of Cancer Research, 1991
- Oral administration of the renal carcinogen, potassium bromate, specifically produces 8-hydroxydeoxyguanosine in rat target organ DNACarcinogenesis, 1987
- Free-radical production and oxidative reactions of hemoglobin.Environmental Health Perspectives, 1985