Aldehyde and xanthine oxidase activities in tissues of streptozotocin- induced diabetic rats: Effects of vitamin e and selenium supplementation
dc.contributor.author | Ghaffari, T | |
dc.contributor.author | Nouri, M | |
dc.contributor.author | Saei, AA | |
dc.contributor.author | Rashidi, M-R | |
dc.date.accessioned | 2018-08-26T08:33:40Z | |
dc.date.available | 2018-08-26T08:33:40Z | |
dc.date.issued | 2012 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52458 | |
dc.description.abstract | Effects 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.iso | English | |
dc.relation.ispartof | Biological Trace Element Research | |
dc.subject | aldehyde | |
dc.subject | alpha tocopherol | |
dc.subject | aryldialkylphosphatase 1 | |
dc.subject | glucose | |
dc.subject | glutathione peroxidase | |
dc.subject | malonaldehyde | |
dc.subject | oxidized low density lipoprotein | |
dc.subject | sodium selenite | |
dc.subject | streptozocin | |
dc.subject | superoxide dismutase | |
dc.subject | xanthine oxidase | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | antidiabetic activity | |
dc.subject | antioxidant activity | |
dc.subject | article | |
dc.subject | controlled study | |
dc.subject | diabetes mellitus | |
dc.subject | drug mechanism | |
dc.subject | enzyme activity | |
dc.subject | enzyme repression | |
dc.subject | female | |
dc.subject | glucose blood level | |
dc.subject | liver level | |
dc.subject | nonhuman | |
dc.subject | oxidative stress | |
dc.subject | rat | |
dc.subject | streptozocin diabetes | |
dc.subject | tissue distribution | |
dc.subject | tissue injury | |
dc.subject | vitamin supplementation | |
dc.subject | Aldehyde Oxidase | |
dc.subject | Animals | |
dc.subject | Antioxidants | |
dc.subject | Aryldialkylphosphatase | |
dc.subject | Blood Glucose | |
dc.subject | Diabetes Mellitus, Experimental | |
dc.subject | Dietary Supplements | |
dc.subject | Erythrocytes | |
dc.subject | Female | |
dc.subject | Glutathione Peroxidase | |
dc.subject | Kidney | |
dc.subject | Lipids | |
dc.subject | Liver | |
dc.subject | Malondialdehyde | |
dc.subject | Rats | |
dc.subject | Rats, Sprague-Dawley | |
dc.subject | Sodium Selenite | |
dc.subject | Streptozocin | |
dc.subject | Superoxide Dismutase | |
dc.subject | Vitamin E | |
dc.subject | Vitamins | |
dc.subject | Xanthine Oxidase | |
dc.subject | Animalia | |
dc.subject | Rattus | |
dc.title | Aldehyde and xanthine oxidase activities in tissues of streptozotocin- induced diabetic rats: Effects of vitamin e and selenium supplementation | |
dc.type | Review | |
dc.citation.volume | 147 | |
dc.citation.issue | 2-3 | |
dc.citation.spage | 217 | |
dc.citation.epage | 225 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.1007/s12011-011-9291-7 |
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