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WDR5在大鼠肾脏缺血再灌注损伤中的作用及机制研究
引用本文:张伍,刘修恒,王磊.WDR5在大鼠肾脏缺血再灌注损伤中的作用及机制研究[J].微循环学杂志,2021(1):7-12.
作者姓名:张伍  刘修恒  王磊
作者单位:1.武汉大学人民医院泌尿外科
基金项目:国家自然科学青年基金(82000639)。
摘    要:目的:探讨WDR5基因在肾脏缺血再灌注损伤中的作用及机制.方法:成年雄性SD大鼠48只,按照随机数表法分为对照组、缺血再灌注损伤组(IR组)、药物溶剂组(DMSO组)、WDR5-0103低剂量组(1mg/kg)、WDR5-0103中剂量组(5mg/kg)、WDR5-0103高剂量组(25mg/kg).对照组:仅切除大鼠...

关 键 词:肾缺血再灌注损伤  WDR5  WDR5-0103  凋亡  炎症因子  TLR4/NF-κB

The Role and Mechanism of WDR5 in Rat Renal Ischemia Reperfusion Injury
ZHANG Wu,LIU Xiu-heng,WANG Lei.The Role and Mechanism of WDR5 in Rat Renal Ischemia Reperfusion Injury[J].Chinese Journal of Microcirculation,2021(1):7-12.
Authors:ZHANG Wu  LIU Xiu-heng  WANG Lei
Institution:(Department of Urology, Renmin Hospital of Wuhan University, Wuhan 430060, China)
Abstract:Objective:To investigate the role and mechanism of WDR5 gene in renal ischemia reperfusion injury.Method:48 adult male SD rats were divided into control group,ischemia reperfusion injury group(IR group),medicine solvent group(DMSO group),WDR5-0103 low dose group(1mg/kg),WDR5-0103 medium dose group(5mg/kg),WDR5-0103 high dose group(25mg/kg).Control group:only the right kidney of the rat was removed;IR group:after the right kidney was removed,the left kidney renal pedicle vessel of the rat was clamped with a non-traumatic vascular clip for 45 minutes.The vascular clip was released to restore blood flow and reperfusion to simulate ischemia and reperfusion.DMSO group:the operation was the same as the I/R group,the left renal blood vessel was closed for 45 minutes,and DMSO was injected intraperitoneally after the vascular clamp was released;WDR5-0103 group:before the establishment of the IR model,different concentrations of WDR5-0103 were injected intraperitoneally.Serum urea nitrogen and creatinine levels in each group of rats were detected immunohistochemical staining was used to detect changes of WDR5 protein expression,TUNEL staining was used to detect cell apoptosis,Realtime-PCR was used to detect TNF-α,IL-1βand ICAM-1 expression levels,Western Blot was used to detect TLR4 protein and NF-κB protein expression.Results:Compared with the control group,the blood Cr and BUN levels of the rats in the IR group increased,the renal tissue WDR5 protein level increased,the renal tissue was significantly adjusted:the number of apoptotic cells increased,and the levels of TNF-α,IL-1βand ICAM-1 The mRNA level was significantly increased,and the TLR4/NF-κB protein expression level was significantly increased(all P<0.01);compared with the IR group,the blood Cr and BUN levels of the WDR5-0103 group at different concentrations were significantly reduced,and the 25mg/kg group was most obvious;WDR5-0103 high-dose group WDR5 protein expression decreased;the pathological damage of rat kidney tissue was reduced,and the number of apoptotic cells was significantly reduced;TNF-α,IL-1βand ICAM-1 mRNA levels were significantly decreased;TLR4/NF-κB The expression level of NF-κB was significantly reduced(all P<0.01).Conclusion:WDR5-0103 can alleviate cell apoptosis and inflammatory response after IR,thereby regulate renal ischemia-reperfusion injury.The mechanism may be related to down-regulation of TLR4/NF-κB pathway.
Keywords:Ischemia reperfusion injury  WDR5  WDR5-0103  Apoptosis  Inflammatory factors  TLR4/NF-κB
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