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      Dose-Dependent Effect of Deltamethrin in Testis, Liver, and Kidney of Wistar Rats

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          Abstract

          Objectives:

          Deltamethrin is a synthetic pyrethroid insecticide used worldwide in agriculture, household pest control, protection of foodstuff, and disease vector control. Although initially thought to be least toxic, a number of recent reports showed its toxic effects in mammalian and non-mammalian animal species. The current study was performed to assess the dose-dependent deltamethrin toxicity on testes, liver, and kidney of male Wistar rats.

          Materials and Methods:

          Twenty-four rats were divided in four groups of 6 each. Group A served as normal control. Group B, C, and D were administered with different doses (2 or 3 or 6 mg/kg corresponding to 1/30 th or 1/20 th or 1/10 th of LD 50, respectively) of deltamethrin for 28 days.

          Results:

          Deltamethrin exposure caused a significant reduction in weight of reproductive organs, decrease in sperm count, sperm motility, serum testosterone (T), follicle stimulating hormones (FSH), and luteinizing hormones (LH) in testis. Glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), glutathione S transferase (GST), glutathione reductase (GR), glutathione peroxidase (GPx) were decreased in testis, liver and kidney of exposed rats. Deltamethrin exposure significantly increased sperm abnormalities in testis. Significant increase in lipid peroxidation (LPO) level was observed in testis, liver and kidney. Deltamethrin also caused histological alterations in testes, liver, and kidney.

          Conclusions:

          The results indicated that deltamethrin at a dose of 6 mg/kg exerts significant harmful effects on testes, liver and kidney as compare to 2 mg and 3 mg/kg. The study concluded that the system toxicity induced by deltamethrin was dose dependent.

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          Most cited references39

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          Selenium: biochemical role as a component of glutathione peroxidase.

          When hemolyzates from erythrocytes of selenium-deficient rats were incubated in vitro in the presence of ascorbate or H(2)O(2), added glutathione failed to protect the hemoglobin from oxidative damage. This occurred because the erythrocytes were practically devoid of glutathione-peroxidase activity. Extensively purified preparations of glutathione peroxidase contained a large part of the (75)Se of erythrocytes labeled in vivo. Many of the nutritional effects of selenium can be explained by its role in glutathione peroxidase.
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            A modified spectrophotometric assay of superoxide dismutase.

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              The changing faces of glutathione, a cellular protagonist.

              Glutathione (GSH) has been described for a long time just as a defensive reagent against the action of toxic xenobiotics (drugs, pollutants, carcinogens). As a prototype antioxidant, it has been involved in cell protection from the noxious effect of excess oxidant stress, both directly and as a cofactor of glutathione peroxidases. In addition, it has long been known that GSH is capable of forming disulfide bonds with cysteine residues of proteins, and the relevance of this mechanism ("S-glutathionylation") in regulation of protein function is currently receiving confirmation in a series of research lines. Rather paradoxically, however, recent studies have also highlighted the ability of GSH-and notably of its catabolites-to promote oxidative processes, by participating in metal ion-mediated reactions eventually leading to formation of reactive oxygen species and free radicals. A crucial role in these phenomena is played by membrane bound gamma-glutamyltransferase activity. The significance of GSH as a major factor in regulation of cell life, proliferation, and death, should be regarded as the integrated result of all these roles it can play.
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                Author and article information

                Journal
                Toxicol Int
                Toxicol Int
                TI
                Toxicology International
                Medknow Publications & Media Pvt Ltd (India )
                0971-6580
                0976-5131
                May-Aug 2014
                : 21
                : 2
                : 131-139
                Affiliations
                [1]Department of Zoology, Bundelkhand University, Jhansi, Uttar Pradesh, India
                [1 ]Department of Biomedical Sciences, Bundelkhand University, Jhansi, Uttar Pradesh, India
                Author notes
                Address for correspondence: Dr. Rambir Singh, Department of Biomedical Sciences, Bundelkhand University, Jhansi, Uttar Pradesh - 284 128, India. E-mail: sehrawat_r@ 123456yahoo.com
                Article
                TI-21-131
                10.4103/0971-6580.139789
                4170553
                25253921
                eef55486-2d9f-447e-9408-da5b745f69e6
                Copyright: © Toxicology International

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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                Categories
                Original Article

                Toxicology
                deltamethrin,kidney,liver,oxidative stress,testes,wistar rats
                Toxicology
                deltamethrin, kidney, liver, oxidative stress, testes, wistar rats

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