Erythropoietin protects against renal ischemia/reperfusion injury in rats via inhibition of oxidative stress, inflammation and apoptosis

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Journal of Contemporary Medical Sciences Pub Date : 2023-08-26 DOI:10.22317/jcms.v9i4.1405
Elaf R. Alaasam, Ali M. Janabi
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 Methods: twenty-eight male rats of Sprague Dawley randomized into four groups: Sham, Iscemia/Reperfusion, NS, and Erythropoietin. Sham group treated kidneys identically without clamping pedicles. Ischemia/Reperfusion group underwent midline laparotomy, 30 minutes ischemia, 2 hours reperfusion, Rats received NS vehicle for Erythropoietin 30 minutes before ischemia, Erythropoietin dose administered 30 minutes before ischemia/reperfusion. Operation performed under maintained anesthesia using ketamine and xylazine injections.
 Results: Renal ischemia /reperfusion increased serum Cr, BUN, IL-1β, NF-kB, Caspase-3, while SOD, GSH, Bcl-2 decreased in induced rats. Erythropoietin treatment reduced Cr and BUN levels, Reduced inflammation, and inflammatory markers. Renal tissue antioxidant markers increased; apoptotic markers decreased. Significant increase in Bcl-2 antiapoptotic marker. Erythropoietin-treated group had significantly better renal histological score compared to induced group.
 Conclusion: Erythropoietin protects against Ischemia/Reperfusion-mediated renal injury, possessing antioxidant, anti-inflammatory, and anti-apoptotic properties.","PeriodicalId":42860,"journal":{"name":"Journal of Contemporary Medical Sciences","volume":"174 1","pages":"0"},"PeriodicalIF":0.2000,"publicationDate":"2023-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Contemporary Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22317/jcms.v9i4.1405","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
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Abstract

Objective: Study investigates erythropoietin's nephroprotective effect in adult male rats with renal ischemia and reperfusion injury, examining biochemical parameters and renal tissue alterations. Methods: twenty-eight male rats of Sprague Dawley randomized into four groups: Sham, Iscemia/Reperfusion, NS, and Erythropoietin. Sham group treated kidneys identically without clamping pedicles. Ischemia/Reperfusion group underwent midline laparotomy, 30 minutes ischemia, 2 hours reperfusion, Rats received NS vehicle for Erythropoietin 30 minutes before ischemia, Erythropoietin dose administered 30 minutes before ischemia/reperfusion. Operation performed under maintained anesthesia using ketamine and xylazine injections. Results: Renal ischemia /reperfusion increased serum Cr, BUN, IL-1β, NF-kB, Caspase-3, while SOD, GSH, Bcl-2 decreased in induced rats. Erythropoietin treatment reduced Cr and BUN levels, Reduced inflammation, and inflammatory markers. Renal tissue antioxidant markers increased; apoptotic markers decreased. Significant increase in Bcl-2 antiapoptotic marker. Erythropoietin-treated group had significantly better renal histological score compared to induced group. Conclusion: Erythropoietin protects against Ischemia/Reperfusion-mediated renal injury, possessing antioxidant, anti-inflammatory, and anti-apoptotic properties.
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促红细胞生成素通过抑制氧化应激、炎症和细胞凋亡对大鼠肾缺血再灌注损伤具有保护作用
目的:研究促红细胞生成素对肾缺血再灌注损伤成年雄性大鼠的肾保护作用,观察其生化指标及肾组织改变。方法:雄性Sprague Dawley大鼠28只,随机分为Sham组、缺血/再灌注组、NS组和促红细胞生成素组。假手术组与对照组治疗肾脏相同,不夹持蒂。缺血/再灌注组大鼠行剖腹正中探查,缺血30 min,再灌注2 h,缺血前30 min给予NS载药促红细胞生成素,缺血/再灌注前30 min给药促红细胞生成素。手术在持续麻醉下注射氯胺酮和噻嗪。 结果:肾缺血/再灌注诱导大鼠血清Cr、BUN、IL-1β、NF-kB、Caspase-3升高,SOD、GSH、Bcl-2降低。促红细胞生成素治疗降低了Cr和BUN水平,减少了炎症和炎症标志物。肾组织抗氧化指标升高;凋亡标记物减少。Bcl-2抗凋亡标志物显著升高。促红细胞生成素治疗组肾脏组织学评分明显优于诱导组。 结论:促红细胞生成素具有抗氧化、抗炎和抗凋亡的作用,对缺血/再灌注介导的肾损伤具有保护作用。
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Journal of Contemporary Medical Sciences
Journal of Contemporary Medical Sciences MEDICINE, GENERAL & INTERNAL-
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65
审稿时长
12 weeks
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