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dc.contributor.authorAhmadiasl, N
dc.contributor.authorBanaei, S
dc.contributor.authorAlihemmati, A
dc.contributor.authorBaradaran, B
dc.contributor.authorAzimian, E
dc.date.accessioned2018-08-26T06:06:07Z
dc.date.available2018-08-26T06:06:07Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41938
dc.description.abstractRenal ischemia reperfusion (IR) is an important cause of renal dysfunction. It contributes to the development of acute renal failure (ARF). The purpose of this study was to investigate the anti-inflammatory effect of erythropoietin (EPO) and melatonin (MEL), which are known anti-inflammatory and antioxidant agents, in IR-induced renal injury in rats.Male Wistar Albino rats were unilaterally nephrectomized and subjected to 45 min of renal pedicle occlusion followed by 24 h reperfusion. MEL (10mg/kg, i.p) and EPO (5000U/kg, i.p) were administered prior to ischemia. After 24 h reperfusion, blood samples were collected for the determination of total antioxidant capacity (TAC), malondialdehyde (MDA) and serum creatinine levels. Also, renal samples were taken for Immunohistochemical evaluation of Bcl2 and TNF-? (tumor necrosis factor-?) expression.Ischemia reperfusion increased creatinine, TAC, MDA levels and TNF-? expression, also, IR decreased Bcl2 expression. Treatment with EPO or MEL decreased creatinine, MDA levels, and increased TAC level. Also, MEL up-regulated Bcl2 expression and down-regulated TNF-? expression compared with EPO.Treatment with EPO and MEL had a curative effect on renal IR injury. These results may indicate that MEL protects against inflammation and apoptosis better than EPO in renal IR injury.
dc.language.isoEnglish
dc.relation.ispartofAdvanced pharmaceutical bulletin
dc.titleThe anti-inflammatory effect of erythropoietin and melatonin on renal ischemia reperfusion injury in male rats.
dc.typearticle
dc.citation.volume4
dc.citation.issue1
dc.citation.spage49
dc.citation.epage54
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.5681/apb.2014.008


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