نمایش مختصر رکورد

dc.contributor.authorHadipour Moradi, Fen_US
dc.contributor.authorNazem, Hen_US
dc.contributor.authorBabaeenezhad, Een_US
dc.contributor.authorCheraghi Venool, Aen_US
dc.contributor.authorJafaripour, Len_US
dc.contributor.authorAhmadvand, Hen_US
dc.date.accessioned1401-05-11T18:55:41Zfa_IR
dc.date.accessioned2022-08-02T18:55:42Z
dc.date.available1401-05-11T18:55:41Zfa_IR
dc.date.available2022-08-02T18:55:42Z
dc.date.issued2022-03-01en_US
dc.date.issued1400-12-10fa_IR
dc.identifier.citation(1400). مجله علمی دانشگاه علوم پزشکی بابل, 24(1), 159-168.fa_IR
dc.identifier.issn1561-4107
dc.identifier.issn2251-7170
dc.identifier.urihttp://jbums.org/article-1-10137-en.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/920672
dc.description.abstractBackground and Objective: Reactive oxygen species are the main factors involved in kidney damage during renal ischemia-reperfusion (RIR). Since D-limonene has antioxidant, anti-diabetic, anti-apoptotic, and lipid peroxidation effects, it prevents mitochondrial dysfunction and inhibits ROS, this study was conducted to evaluate the effects of pretreatment with D-limonene on oxidative stress and antioxidant activity in RIR injury. Methods: In this experimental study, 24 male Wistar rats were randomly divided into 3 groups: control, RIR (ischemia was induced by clamping of renal pedicles for 45 minutes and reperfusion was considered 24 hours after ischemia), and RIR+D-limonene (100 mg/kg by oral gavage for 12 days). Serum and kidney were used to evaluate malondialdehyde (MDA), myeloperoxidase (MPO), paraoxonase1 (PON1), glutathione (GSH), catalase (CAT), glutathione peroxidase (GPX), and nitric oxide (NO). Findings: Serum and renal levels of MDA ([18.2±98.77 vs. 9.21±1.77] and [19.85±3.39 vs. 9.84±1.65]) and MPO ([67.25±32.67 vs. 40.21±6.1] and [18.44±2.86 vs. 10.42±1.68]) and serum level of NO (31.3±36.1 vs. 27.88±2.6) significantly increased in the RIR group compared with the control group (p<0.05). Serum and kidney levels of GSH, activities of CAT and GPX in serum and kidney, and serum activity of PON1 significantly decreased in the RIR group compared with the control group (p<0.05). Pretreatment with D-limonene could significantly ameliorate serum and renal levels of MDA, serum levels of GSH and NO, and serum activity of CAT in rats pretreated with D-limonene in comparison with RIR rats (p<0.05). Conclusion: This study indicated that pretreatment with D-limonene could ameliorate RIR injuries in rats through its antioxidant activities.en_US
dc.format.extent349
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherدانشگاه علوم پزشکی بابلfa_IR
dc.relation.ispartofمجله علمی دانشگاه علوم پزشکی بابلfa_IR
dc.relation.ispartofJournal of Babol University Of Medical Sciencesen_US
dc.subjectD-Limoneneen_US
dc.subjectRenal Ischemia-Reperfusionen_US
dc.subjectOxidative Stressen_US
dc.subjectRats.en_US
dc.subjectBiochemicalen_US
dc.titlePretreatment Effect of D-Limonene on Oxidative Stress Induced by Renal Ischemia-Reperfusion Injury in Ratsen_US
dc.typeTexten_US
dc.typeResearchen_US
dc.contributor.department1.Department of Biochemistry, Faculty of Basic Sciences, Payame Noor University, Isfahan, I.R.Iran. 2.Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, I R.Iran.en_US
dc.contributor.department3.Department of Clinical Biochemistry, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, I.R.Iran.en_US
dc.contributor.department4.Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, I.R.Iran.en_US
dc.contributor.department2.Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, I R.Iran.en_US
dc.contributor.department5.Department of Anatomy, Faculty of Medicine, Dezful University of Medical Sciences, Dezful, I.R.Iran.en_US
dc.contributor.department6.Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, Hamadan, I.R.Iran.en_US
dc.citation.volume24
dc.citation.issue1
dc.citation.spage159
dc.citation.epage168


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