J. Lv , X. Wang , S.Y. Liu , P.F. Liang , M. Feng , L.L. Zhang , A.P. Xu
{"title":"Protective effect of Fenofibrate in renal ischemia reperfusion injury: Involved in suppressing kinase 2 (JAK2)/transcription 3 (STAT3)/p53 signaling activation","authors":"J. Lv , X. Wang , S.Y. Liu , P.F. Liang , M. Feng , L.L. Zhang , A.P. Xu","doi":"10.1016/j.patbio.2015.07.010","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>Renal ischemia reperfusion (I/R) injury is a common reason of acute kidney injury. Apoptosis play an important role in the IRI. Fenofibrate, one of agonist Peroxisome proliferator-activated receptor-alpha (PPARα) has the effect of anti-apoptosis. This study was to explore the effect of Fenofibrate on renal ischemia reperfusion injury and its mechanism.</p></div><div><h3>Materials and methods</h3><p>IRI was induced by bilateral renal ischemia for 45<!--> <!-->min followed by reperfusion for 24<!--> <!-->h. Eighteen male C57BL/6 mice were randomly divided into three groups: Sham group (Sham), IRI group (IRI), I/R-Fenofibrate group (FEN). Fenofibrate was injected at 45<!--> <!-->min before renal ischemia. Renal histology, function, and the expression of Bax, Bcl-2, Bcl-xl p21, p53, Caspse3, CytC, p-JAK2, p-STAT3 and p-PPAR-α were assessed.</p></div><div><h3>Results</h3><p>Fenofibrate precondition can significantly alleviate the renal dysfunction, the pathological change, up-regulate the expression of p-PPAR-α, Bcl-2, Bcl-xl, Caspase3 and down-regulate the expression of p-JAK2, p-STAT3, p53, p21, CytC and Bax induced by renal IR injury.</p></div><div><h3>Conclusion</h3><p>Fenofibrate precondition can protect mice against IRI by suppressing p53-mediating apoptosis which was associated with inhibiting JAK2/STAT3 signaling activation though further activating PPAR-α. Our findings suggest that Fenofibrate could be useful for preventing IR-induced renal injury.</p></div>","PeriodicalId":19743,"journal":{"name":"Pathologie-biologie","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.patbio.2015.07.010","citationCount":"25","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathologie-biologie","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0369811415000681","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 25
Abstract
Objective
Renal ischemia reperfusion (I/R) injury is a common reason of acute kidney injury. Apoptosis play an important role in the IRI. Fenofibrate, one of agonist Peroxisome proliferator-activated receptor-alpha (PPARα) has the effect of anti-apoptosis. This study was to explore the effect of Fenofibrate on renal ischemia reperfusion injury and its mechanism.
Materials and methods
IRI was induced by bilateral renal ischemia for 45 min followed by reperfusion for 24 h. Eighteen male C57BL/6 mice were randomly divided into three groups: Sham group (Sham), IRI group (IRI), I/R-Fenofibrate group (FEN). Fenofibrate was injected at 45 min before renal ischemia. Renal histology, function, and the expression of Bax, Bcl-2, Bcl-xl p21, p53, Caspse3, CytC, p-JAK2, p-STAT3 and p-PPAR-α were assessed.
Results
Fenofibrate precondition can significantly alleviate the renal dysfunction, the pathological change, up-regulate the expression of p-PPAR-α, Bcl-2, Bcl-xl, Caspase3 and down-regulate the expression of p-JAK2, p-STAT3, p53, p21, CytC and Bax induced by renal IR injury.
Conclusion
Fenofibrate precondition can protect mice against IRI by suppressing p53-mediating apoptosis which was associated with inhibiting JAK2/STAT3 signaling activation though further activating PPAR-α. Our findings suggest that Fenofibrate could be useful for preventing IR-induced renal injury.
目的肾缺血再灌注(I/R)损伤是急性肾损伤的常见原因。细胞凋亡在IRI中起重要作用。非诺贝特是过氧化物酶体增殖激活受体α (PPARα)的激动剂之一,具有抗细胞凋亡的作用。本研究旨在探讨非诺贝特对肾缺血再灌注损伤的影响及其机制。材料与方法双侧肾缺血45min后再灌注24h,雄性C57BL/6小鼠18只,随机分为3组:Sham组(Sham)、IRI组(IRI)、I/ r -非诺贝特组(FEN)。非诺贝特于肾缺血前45分钟注射。评估肾脏组织学、功能及Bax、Bcl-2、Bcl-xl p21、p53、Caspse3、CytC、p-JAK2、p-STAT3、p-PPAR-α的表达。结果非诺贝特预处理能显著缓解肾IR损伤大鼠肾功能不全及病理改变,上调p-PPAR-α、Bcl-2、Bcl-xl、Caspase3的表达,下调p-JAK2、p-STAT3、p53、p21、CytC和Bax的表达。结论非诺贝特预处理可通过进一步激活PPAR-α,抑制p53介导的细胞凋亡,从而抑制JAK2/STAT3信号通路的激活,从而对IRI小鼠具有保护作用。我们的研究结果表明,非诺贝特可用于预防ir引起的肾损伤。