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Biochemical and Molecular Evidences on the Protection by Magnesium Oxide Nanoparticles of Chlorpyrifos-Induced Apoptosis in Human Lymphocytes Publisher



Heydary V1, 2, 3 ; Navaeinigjeh M1, 2, 4 ; Rahimifard M1, 2 ; Mohammadirad A1, 2 ; Baeeri M1, 2 ; Abdollahi M1, 2, 3, 4, 5
Authors
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Authors Affiliations
  1. 1. Toxicology and Poisoning Research Center, Ahar, Iran
  2. 2. Pharmaceutical Sciences Research Center, Ahar, Iran
  3. 3. Islamic Azad University, Ahar Branch, Ahar, Iran
  4. 4. Department of Tissue Engineering, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Research in Medical Sciences Published:2015


Abstract

Background: Chlorpyrifos (CP) is one of the most widely used organophosphate (OP) insecticides in agricultural and residential pest control with its attendant adverse health effect. In the present study, it is proposed to investigate the possible modulatory role of magnesium oxide nanoparticles (MgO NPs) against CP-induced toxicity in human lymphocytes and determine the mechanisms lying behind this protection by viability and biochemical assays. Materials and Methods: Isolated lymphocytes were exposed to 12 μg/mL CP either alone or in combination with different concentrations of MgO NPs (0.1 μg/mL, 1 μg/mL, 10 μg/mL, and 100 μg/mL). After a 3-day incubation, the viability and oxidative stress markers including cellular mitochondrial activity, caspase-3 and -9 activities, total antioxidant power, lipid peroxidation, and myeloperoxidase (MPO) activity were measured. Also, the levels of tumor necrosis factor-α (TNF-α) as inflammatory index, along with acetylcholinesterase (AChE) activity were measured. Statistical differences were determined using one-way analysis of variance (ANOVA) and Dunnett’s multiple comparison tests. Results: It is indicated that CP-exposed lymphocytes treated with MgO NPs resulted in a substantial reduction in the pace of mortality as well as the stages of oxidative stress in a dose-dependent manner. Also, MgO NPs (100 μg/mL) meaningfully restored CP-induced increase of TNF-α (P<0.001) and decrease of AChE activity (P<0.001) and were capable of preventing CP-treated human lymphocytes from apoptosis (P<0.001). Conclusion: Our results demonstrate that MgO NPs in approximate 100 nm diameter not only make cells resistant to the toxic properties of CP but also attenuate toxic effects of CP, which is demonstrating the potential of MgO NPs to be applied in future immune deficiency therapeutic strategies. © 2015 Journal of Research in Medical Sciences.
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