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dc.contributor.authorSoufi, FG
dc.contributor.authorMohammad-nejad, D
dc.contributor.authorAhmadieh, H
dc.date.accessioned2018-08-26T08:04:27Z
dc.date.available2018-08-26T08:04:27Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49570
dc.description.abstractBackground: This study was designed to investigate the possible effectiveness of resveratrol (trans-3,5,4'-trihydroxystilbene) administration on oxidative stress, nuclear factor kappa B (NF-kappa B) activity and apoptosis rate in streptozotocin-nicotinamide-induced diabetic retinopathy. Methods: Male Wistar rats were divided into four groups: normal control, diabetic control, normal rats treated with resveratrol, and diabetic rats treated with resveratrol. Diabetes was induced by injection of streptozotocin (50 mg/kg; ip), 15 min after the prescription of nicotinamide ( 110 mg/kg; ip) in 12 h fasted rats. Results: Four-month oral resveratrol administration (5 mg/kg/day) significantly alleviated hyperglycemia, weight loss, enhancement of oxidative markers (lipid peroxidation index and oxidized to reduced glutathione ratio) and superoxide dismutase activity in both blood and retinas of the diabetic rats. Moreover, resveratrol administration to diabetic rats improved the elevated levels of retinas NF-kappa B activity and apoptosis rate. On the other hand, four months resveratrol administration prevented from disarrangement and reduction in thickness of retinal layers. Conclusion: These beneficial antidiabetic observations suggest that resveratrol may be considered as a therapeutic supplement to prevent from diabetic retinopathy.
dc.language.isoEnglish
dc.relation.ispartofPHARMACOLOGICAL REPORTS
dc.subjectdiabetes
dc.subjectantioxidant
dc.subjecthyperglycemia
dc.subjectredox status
dc.subjectcell death
dc.titleResveratrol improves diabetic retinopathy possibly through oxidative stress - nuclear factor kappa B - apoptosis pathway
dc.typeArticle
dc.citation.volume64
dc.citation.issue6
dc.citation.spage1505
dc.citation.epage1514
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/S1734-1140(12)70948-9


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