2011
DOI: 10.1016/j.ecoenv.2010.11.007
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Antioxidant effect of vitamin E and selenium on hepatotoxicity induced by dimethoate in female adult rats

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Cited by 53 publications
(31 citation statements)
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“…However, the co-treatment of Se plus Zn has reduced the histological alterations induced by MD, which might be attributed to their antiradical/antioxidant roles. Moreover, these results are in good accordance with those obtained by other studies which have postulated the beneficial role of Se and Zn on histopathological and enzymatic changes of rats (Goel et al, 2005;Ben Amara et al, 2010;Heikal et al, 2012). Though, the beneficial role of Se and Zn in reducing oxidative stress parameters in the present study might be related to its mild antioxidant potential against toxins induced hepatotoxicity.…”
Section: Discussionsupporting
confidence: 82%
“…However, the co-treatment of Se plus Zn has reduced the histological alterations induced by MD, which might be attributed to their antiradical/antioxidant roles. Moreover, these results are in good accordance with those obtained by other studies which have postulated the beneficial role of Se and Zn on histopathological and enzymatic changes of rats (Goel et al, 2005;Ben Amara et al, 2010;Heikal et al, 2012). Though, the beneficial role of Se and Zn in reducing oxidative stress parameters in the present study might be related to its mild antioxidant potential against toxins induced hepatotoxicity.…”
Section: Discussionsupporting
confidence: 82%
“…It has been shown to be effective in reducing exercise-induced oxidative stress in rats (Metin et al, 2002). In addition, these findings are in good agreement with those obtained by other studies which postulated the beneficial role of vitamin E and vitamin C on histological and enzymatic changes of rats (Das et al, 2006;Ben Amara et al, 2010). Therefore, the supplementation of vitamin E or vitamin C had protected liver function from cadmium intoxication as indicated by the significant restoration of serum total protein, albumin, serum glucose, GOT, GPT and alkaline phosphatase.…”
Section: Discussionsupporting
confidence: 82%
“…Previous studies indicate that dimethoate leads to oxidative stress via production of free radicals and induction of lipid peroxidation [4][5][6] . Some studies have shown that dimethoate causes significant increase in lipid peroxidation by interacting with membrane lipids due to its lipophilic feature [7,8] . It has been noticed the dimethoate toxicity results in deleterious effects on various organs such as liver, brain, testes, pancreas of rats [9] .…”
Section: Introductionmentioning
confidence: 99%