نمایش مختصر رکورد

dc.contributor.authorHavakhah, Shahrzaden_US
dc.contributor.authorSadeghnia, Hamid Ren_US
dc.contributor.authorHajzadeh, Mosa-Al-Rezaen_US
dc.contributor.authorMohammadian Roshan, Namaen_US
dc.contributor.authorShafiee, Somayehen_US
dc.contributor.authorHosseinzadeh, Hosseinen_US
dc.contributor.authorMohareri, Nargesen_US
dc.contributor.authorKhajavi Rad, Abolfazlen_US
dc.date.accessioned1399-07-09T08:24:32Zfa_IR
dc.date.accessioned2020-09-30T08:24:32Z
dc.date.available1399-07-09T08:24:32Zfa_IR
dc.date.available2020-09-30T08:24:32Z
dc.date.issued2014-12-01en_US
dc.date.issued1393-09-10fa_IR
dc.date.submitted2015-01-20en_US
dc.date.submitted1393-10-30fa_IR
dc.identifier.citationHavakhah, Shahrzad, Sadeghnia, Hamid R, Hajzadeh, Mosa-Al-Reza, Mohammadian Roshan, Nama, Shafiee, Somayeh, Hosseinzadeh, Hossein, Mohareri, Narges, Khajavi Rad, Abolfazl. (2014). Effect of Nigella sativa on ischemia-reperfusion induced rat kidney damage. Iranian Journal of Basic Medical Sciences, 17(12), 986-992. doi: 10.22038/ijbms.2015.3856en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.urihttps://dx.doi.org/10.22038/ijbms.2015.3856
dc.identifier.urihttp://ijbms.mums.ac.ir/article_3856.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/340848
dc.description.abstract<em>Objective(s):</em>There are a few previously reported studies about the effect of <em>Nigella</em><em> sativa</em> oil on renal ischemia-reperfusion injury (IRI). The aim of the present study was to test the hypothesis whether pre- or post-treatment with <em>N. sativa</em> hydroalcoholic extract (NSE) would reduce tissue injury and oxidative damages in a clinically relevant rat model of renal IRI.    <br/><em>Materials and Methods:</em> IRI was induced by clamping of bilateral renal arteries for 40 min fallowed by reperfusion for 180 min. NSE was prepared in a Soxhlet extractor and administrated with doses of 150 mg/kg or 300 mg/kg at 1 hr before ischemia induction (P-150 and 300) or at the beginning of reperfusion phase (T-150 and 300), via jugular catheter intravenously. The kidneys were then removed and subjected to biochemical analysis, comet assay or histopathological examination. <br/><em>Results:</em> The kidneys of untreated IRI rats had a higher histopathological score (<em>P</em><0.001), while in P-150, as well as T-150 and T-300 groups tubular lesions significantly decreased (<em>P</em><0.001). Pre- and post-treatment with NSE also resulted in a significant decrease in malondialdehyde (MDA) level (<em>P</em><0.001) and DNA damage (<em>P</em><0.001) that were increased by renal I/R injury. NSE treatment also significantly restore (<em>P</em><0.01) the decrease in renal thiol content caused by IRI. <br/><em>Conclusion:</em> The present study shows <em>N. sativa</em> extract has marked protective action against renal IRI, which may be partly due to its antioxidant effects.en_US
dc.format.extent1734
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Basic Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijbms.2015.3856
dc.subjectComet assayen_US
dc.subjectIschemia-reperfusion injury (IRI)en_US
dc.subjectKidneyen_US
dc.subjectNigella Sativaen_US
dc.subjectOxidative stressen_US
dc.titleEffect of Nigella sativa on ischemia-reperfusion induced rat kidney damageen_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmacological Research Center of Medicinal Plants, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentNeurocognitive Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Pathology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentNeuroinflammation Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.citation.volume17
dc.citation.issue12
dc.citation.spage986
dc.citation.epage992


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