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A step forward toward establishing a novel preclinical porcine model to study ischemia/reperfusion-induced acute and chronic kidney injures.朝着建立一种新型临床前猪模型以研究缺血/再灌注诱导的急性和慢性肾损伤迈出了一步。
Transl Androl Urol. 2022 May;11(5):575-577. doi: 10.21037/tau-22-176.
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[Ischemia-reperfusion injury after kidney transplantation].[肾移植后的缺血再灌注损伤]
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Development of a novel porcine ischemia/reperfusion model inducing different ischemia times in bilateral kidneys-effects of hydrogen gas inhalation.一种新型猪双侧肾脏不同缺血时间缺血/再灌注模型的建立——氢气吸入的影响
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Explicit role of peroxisome proliferator-activated receptor gamma in gallic acid-mediated protection against ischemia-reperfusion-induced acute kidney injury in rats.过氧化物酶体增殖物激活受体 γ 在没食子酸介导的对抗大鼠缺血再灌注诱导的急性肾损伤中的明确作用。
J Surg Res. 2014 Apr;187(2):631-9. doi: 10.1016/j.jss.2013.11.1088. Epub 2013 Nov 22.
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Sildenafil obviates ischemia-reperfusion injury-induced acute kidney injury through peroxisome proliferator-activated receptor γ agonism in rats.西地那非通过激活大鼠体内过氧化物酶体增殖物激活受体γ来减轻缺血再灌注损伤诱导的急性肾损伤。
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A Translational Study of a New Therapeutic Approach for Acute Myocardial Infarction: Nanoparticle-Mediated Delivery of Pitavastatin into Reperfused Myocardium Reduces Ischemia-Reperfusion Injury in a Preclinical Porcine Model.急性心肌梗死新治疗方法的转化研究:纳米颗粒介导匹伐他汀递送进入再灌注心肌可减轻临床前猪模型中的缺血再灌注损伤
PLoS One. 2016 Sep 7;11(9):e0162425. doi: 10.1371/journal.pone.0162425. eCollection 2016.

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A clinically-relevant mouse model that displays hemorrhage exacerbates tourniquet-induced acute kidney injury.一种表现出出血的临床相关小鼠模型会加重止血带诱导的急性肾损伤。
Front Physiol. 2023 Nov 8;14:1240352. doi: 10.3389/fphys.2023.1240352. eCollection 2023.

本文引用的文献

1
Development of a novel porcine ischemia/reperfusion model inducing different ischemia times in bilateral kidneys-effects of hydrogen gas inhalation.一种新型猪双侧肾脏不同缺血时间缺血/再灌注模型的建立——氢气吸入的影响
Transl Androl Urol. 2022 Apr;11(4):430-438. doi: 10.21037/tau-21-1164.
2
Tourniquet-induced lower limb ischemia/reperfusion reduces mitochondrial function by decreasing mitochondrial biogenesis in acute kidney injury in mice.止血带引起的下肢缺血/再灌注通过减少急性肾损伤小鼠的线粒体生物发生来降低线粒体功能。
Physiol Rep. 2022 Feb;10(3):e15181. doi: 10.14814/phy2.15181.
3
Porcine models of acute kidney injury.猪的急性肾损伤模型。
Am J Physiol Renal Physiol. 2021 Jun 1;320(6):F1030-F1044. doi: 10.1152/ajprenal.00022.2021. Epub 2021 Apr 26.
4
Large animal models for translational research in acute kidney injury.急性肾损伤转化研究的大动物模型。
Ren Fail. 2020 Nov;42(1):1042-1058. doi: 10.1080/0886022X.2020.1830108.
5
Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers.传统猪作为人类肾脏药物排泄过程的动物模型:通过使用外源性标志物混合物解析猪的肾功能
Front Pharmacol. 2020 Jun 12;11:883. doi: 10.3389/fphar.2020.00883. eCollection 2020.
6
The pig as a model for immunology research.猪作为免疫学研究的模型。
Cell Tissue Res. 2020 May;380(2):287-304. doi: 10.1007/s00441-020-03206-9. Epub 2020 Apr 30.
7
Haemodynamics Imaging of Swine Segmental Kidney Artery Using Duplex Doppler Technique.使用双功多普勒技术对猪节段性肾动脉进行血流动力学成像
J Vet Res. 2019 Jun 12;63(2):259-265. doi: 10.2478/jvetres-2019-0036. eCollection 2019 Jun.
8
Resident macrophages reprogram toward a developmental state after acute kidney injury.急性肾损伤后,驻留巨噬细胞会重编程为一种发育状态。
JCI Insight. 2019 Jan 24;4(2):e125503. doi: 10.1172/jci.insight.125503.
9
Extracorporeal shock wave treatment attenuated left ventricular dysfunction and remodeling in mini-pig with cardiorenal syndrome.体外冲击波治疗减轻了心肾综合征小型猪的左心室功能障碍和重塑。
Oncotarget. 2017 May 30;8(33):54747-54763. doi: 10.18632/oncotarget.18287. eCollection 2017 Aug 15.
10
An in-depth comparison of the porcine, murine and human inflammasomes; lessons from the porcine genome and transcriptome.猪、小鼠和人类炎性小体的深入比较;来自猪基因组和转录组的经验教训。
Vet Microbiol. 2017 Apr;202:2-15. doi: 10.1016/j.vetmic.2016.05.013. Epub 2016 Jun 4.

A step forward toward establishing a novel preclinical porcine model to study ischemia/reperfusion-induced acute and chronic kidney injures.

作者信息

Zhou Xiaoming

机构信息

Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.

出版信息

Transl Androl Urol. 2022 May;11(5):575-577. doi: 10.21037/tau-22-176.

DOI:10.21037/tau-22-176
PMID:35693710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9177254/
Abstract
摘要