The effect of 2,2-dichlorovinyl
dimethyl phosphate on redox homeostasis in male rats was investigated. Rats were grouped into four: A, B, C and D where A (the control) received orally 1 ml of distilled water; B, C and D (test groups) received orally 2.5, 5 and 10mg/kg
body weight of
DDVP respectively for 28 days.
DDVP administration significantly reduced (P<0.05) the
alkaline phosphatase activity in the liver and kidney with corresponding increases in the serum.
Acid phosphatase activity increased significantly (P<0.05) in liver and kidney, while there was no significant change (P>0.05) in the serum
acid phosphatase activity. There was also a significant decrease (P<0.05) in the activities of
superoxide dismutase,
catalase,
glutathione peroxidase and
glutathione reductase in the liver and kidney. Liver and kidney levels of GSH,
vitamins C and E were also significantly reduced (P<0.05). Serum malonidialdehyde and
lipid hydroperoxide also increased significantly (P<0.05) in all
DDVP treated groups. The available data from this study revealed that
DDVP brings about its toxicity through depletion of the
antioxidant systems and thus exposing the cells and cellular macromolecules to oxidative attacks by
reactive oxygen species generated either from its metabolites or other in vivo means.