Yichen Jia, Long Zheng, Long Li, Jiawei Li, Ming Xu, T. Zhu
{"title":"ETaR siRNA通过改变肾脏免疫微环境对大鼠肾缺血再灌注损伤的保护作用","authors":"Yichen Jia, Long Zheng, Long Li, Jiawei Li, Ming Xu, T. Zhu","doi":"10.3760/CMA.J.ISSN.0254-1785.2019.02.002","DOIUrl":null,"url":null,"abstract":"Objective \nTo explore the protective effect of ETaR siRNA on renal ischemia reperfusion injury (IRI) by changing the immuno-microenvironment in rats. \n \n \nMethods \nA total of 40 male Sprague-Dawley (SD) rats were randomized into four groups of sham, IR, negative siRNA and ETaR siRNA. A renal IRI model was generated by clamping left renal artery. ETaR siRNA was delivered into kidney through renal vein by a retrograde 'hydrodynamic’ injection. Blood samples were collected for detecting renal function and kidney tissue harvested for Hematoxylin & Eosin (HE) staining, TdT-mediated dUTP Nick-End Labeling (TUNEL) staining, polymerase chain reaction (PCR) and Western blot at 48 h post-reperfusion. \n \n \nResults \nSerum creatinine, blood urea nitrogen and renal apoptotic cells increased and renal tissue was injured after IR. The changes were inhibited by ETaR siRNA. PCR showed that ETaR siRNA treatment significantly down-regulated the expressions of inflammatory factors TNF-α, IFN-γ and IL-6 and transcription factor NF-κB induced by IR. \n \n \nConclusions \nETaR siRNA can effectively improve the immuno-microenvironment and thereby alleviate renal ischemia reperfusion injury. \n \n \nKey words: \nRats; Kidney; Endothelin receptor; Small interfering RNA; Immuno-microenvironment; Reperfusion injury","PeriodicalId":9885,"journal":{"name":"Chineae Journal of Organ Transplantation","volume":"71 1","pages":"68-71"},"PeriodicalIF":0.0000,"publicationDate":"2019-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Protective effect of ETaR siRNA on renal ischemia-reperfusion injury in rats by changing the immuno-microenvironment of kidney\",\"authors\":\"Yichen Jia, Long Zheng, Long Li, Jiawei Li, Ming Xu, T. Zhu\",\"doi\":\"10.3760/CMA.J.ISSN.0254-1785.2019.02.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo explore the protective effect of ETaR siRNA on renal ischemia reperfusion injury (IRI) by changing the immuno-microenvironment in rats. \\n \\n \\nMethods \\nA total of 40 male Sprague-Dawley (SD) rats were randomized into four groups of sham, IR, negative siRNA and ETaR siRNA. A renal IRI model was generated by clamping left renal artery. ETaR siRNA was delivered into kidney through renal vein by a retrograde 'hydrodynamic’ injection. Blood samples were collected for detecting renal function and kidney tissue harvested for Hematoxylin & Eosin (HE) staining, TdT-mediated dUTP Nick-End Labeling (TUNEL) staining, polymerase chain reaction (PCR) and Western blot at 48 h post-reperfusion. \\n \\n \\nResults \\nSerum creatinine, blood urea nitrogen and renal apoptotic cells increased and renal tissue was injured after IR. The changes were inhibited by ETaR siRNA. PCR showed that ETaR siRNA treatment significantly down-regulated the expressions of inflammatory factors TNF-α, IFN-γ and IL-6 and transcription factor NF-κB induced by IR. \\n \\n \\nConclusions \\nETaR siRNA can effectively improve the immuno-microenvironment and thereby alleviate renal ischemia reperfusion injury. \\n \\n \\nKey words: \\nRats; Kidney; Endothelin receptor; Small interfering RNA; Immuno-microenvironment; Reperfusion injury\",\"PeriodicalId\":9885,\"journal\":{\"name\":\"Chineae Journal of Organ Transplantation\",\"volume\":\"71 1\",\"pages\":\"68-71\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chineae Journal of Organ Transplantation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.0254-1785.2019.02.002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chineae Journal of Organ Transplantation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.0254-1785.2019.02.002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Protective effect of ETaR siRNA on renal ischemia-reperfusion injury in rats by changing the immuno-microenvironment of kidney
Objective
To explore the protective effect of ETaR siRNA on renal ischemia reperfusion injury (IRI) by changing the immuno-microenvironment in rats.
Methods
A total of 40 male Sprague-Dawley (SD) rats were randomized into four groups of sham, IR, negative siRNA and ETaR siRNA. A renal IRI model was generated by clamping left renal artery. ETaR siRNA was delivered into kidney through renal vein by a retrograde 'hydrodynamic’ injection. Blood samples were collected for detecting renal function and kidney tissue harvested for Hematoxylin & Eosin (HE) staining, TdT-mediated dUTP Nick-End Labeling (TUNEL) staining, polymerase chain reaction (PCR) and Western blot at 48 h post-reperfusion.
Results
Serum creatinine, blood urea nitrogen and renal apoptotic cells increased and renal tissue was injured after IR. The changes were inhibited by ETaR siRNA. PCR showed that ETaR siRNA treatment significantly down-regulated the expressions of inflammatory factors TNF-α, IFN-γ and IL-6 and transcription factor NF-κB induced by IR.
Conclusions
ETaR siRNA can effectively improve the immuno-microenvironment and thereby alleviate renal ischemia reperfusion injury.
Key words:
Rats; Kidney; Endothelin receptor; Small interfering RNA; Immuno-microenvironment; Reperfusion injury