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dc.contributor.authorGhaffari, T
dc.contributor.authorNouri, M
dc.contributor.authorSaei, AA
dc.contributor.authorRashidi, M-R
dc.date.accessioned2018-08-26T08:33:40Z
dc.date.available2018-08-26T08:33:40Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52458
dc.description.abstractEffects of vitamin E and selenium supplementation on aldehyde oxidase (AO) and xanthine oxidase (XO) activities and antioxidant status in liver, kidney, and heart of streptozotocin (STZ)-induced diabetic rats were examined. AO and XO activities increased significantly after induction of diabetes in rats. Following oral vitamin E (300 mg/kg) and sodium selenite (0.5 mg/kg) intake once a day for 4 weeks, XO activity decreased significantly. AO activity decreased significantly in liver, but remained unchanged in kidney and heart of vitamin E- and selenium-treated rats compared to the diabetic rats. Total antioxidants status, paraoxonase-1 (PON1) and erythrocyte superoxide dismutase activities significantly decreased in the diabetic rats compared to the controls, while a higher fasting plasma glucose level was observed in the diabetic animals. The glutathione peroxidase activity remained statistically unchanged. Malondialdehyde and oxidized low-density lipoprotein levels were higher in the diabetic animals; however, these values were significantly reduced following vitamin E and selenium supplementation. In summary, both AO and XO activities increase in STZ-induced diabetic rats, and vitamin E and selenium supplementation can reduce these activities. The results also indicate that administration of vitamin E and selenium has hypolipidemic, hypoglycemic, and antioxidative effects. It decreases tissue damages in diabetic rats, too. é 2012 Springer Science+Business Media, LLC.
dc.language.isoEnglish
dc.relation.ispartofBiological Trace Element Research
dc.subjectaldehyde
dc.subjectalpha tocopherol
dc.subjectaryldialkylphosphatase 1
dc.subjectglucose
dc.subjectglutathione peroxidase
dc.subjectmalonaldehyde
dc.subjectoxidized low density lipoprotein
dc.subjectsodium selenite
dc.subjectstreptozocin
dc.subjectsuperoxide dismutase
dc.subjectxanthine oxidase
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantidiabetic activity
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectcontrolled study
dc.subjectdiabetes mellitus
dc.subjectdrug mechanism
dc.subjectenzyme activity
dc.subjectenzyme repression
dc.subjectfemale
dc.subjectglucose blood level
dc.subjectliver level
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectrat
dc.subjectstreptozocin diabetes
dc.subjecttissue distribution
dc.subjecttissue injury
dc.subjectvitamin supplementation
dc.subjectAldehyde Oxidase
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectAryldialkylphosphatase
dc.subjectBlood Glucose
dc.subjectDiabetes Mellitus, Experimental
dc.subjectDietary Supplements
dc.subjectErythrocytes
dc.subjectFemale
dc.subjectGlutathione Peroxidase
dc.subjectKidney
dc.subjectLipids
dc.subjectLiver
dc.subjectMalondialdehyde
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectSodium Selenite
dc.subjectStreptozocin
dc.subjectSuperoxide Dismutase
dc.subjectVitamin E
dc.subjectVitamins
dc.subjectXanthine Oxidase
dc.subjectAnimalia
dc.subjectRattus
dc.titleAldehyde and xanthine oxidase activities in tissues of streptozotocin- induced diabetic rats: Effects of vitamin e and selenium supplementation
dc.typeReview
dc.citation.volume147
dc.citation.issue2-3
dc.citation.spage217
dc.citation.epage225
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1007/s12011-011-9291-7


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