Literature DB >> 25064118

Mouse models and methods for studying human disease, acute kidney injury (AKI).

Ganesan Ramesh1, Punithavathi Ranganathan.   

Abstract

Acute kidney injury (AKI) is serious complication in hospitalized patients with high level of mortality. There is not much progress made for the past 50 years in reducing the mortality rate despite advances in understanding disease pathology. Using variety of animal models of acute kidney injury, scientist studies the pathogenic mechanism of AKI and to test therapeutic drugs, which may reduce renal injury. Among them, renal pedicle clamping and cisplatin induced nephrotoxicity in mice are most prominently used, mainly due to the availability of gene knockouts to study specific gene functions, inexpensive and availability of the inbred strain with less genetic variability. However, ischemic mouse model is highly variable and require excellent surgical skills to reduce variation in the observation. In this chapter, we describe a detailed protocol of the mouse model of bilateral renal ischemia-reperfusion and cisplatin induced nephrotoxicity. We also discuss the protocol for the isolation and analysis of infiltrated inflammatory cell into the kidney by flow cytometry. Information provided in this chapter will help scientist who wants to start research on AKI and want to establish the mouse model for ischemic and toxic kidney injury.

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Year:  2014        PMID: 25064118     DOI: 10.1007/978-1-4939-1215-5_24

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  14 in total

1.  A new mouse model of hemorrhagic shock-induced acute kidney injury.

Authors:  Lei Wang; Jiangping Song; Jacentha Buggs; Jin Wei; Shaohui Wang; Jie Zhang; Gensheng Zhang; Yan Lu; Kay-Pong Yip; Ruisheng Liu
Journal:  Am J Physiol Renal Physiol       Date:  2016-11-09

2.  The Kidney Contains Ontogenetically Distinct Dendritic Cell and Macrophage Subtypes throughout Development That Differ in Their Inflammatory Properties.

Authors:  Natallia Salei; Stephan Rambichler; Johanna Salvermoser; Nikos E Papaioannou; Ronja Schuchert; Dalia Pakalniškytė; Na Li; Julian A Marschner; Julia Lichtnekert; Christopher Stremmel; Filippo M Cernilogar; Melanie Salvermoser; Barbara Walzog; Tobias Straub; Gunnar Schotta; Hans-Joachim Anders; Christian Schulz; Barbara U Schraml
Journal:  J Am Soc Nephrol       Date:  2020-01-13       Impact factor: 10.121

3.  Comparison of 99mTc-DMSA renal scintigraphy with biochemical and histopathological findings in animal models of acute kidney injury.

Authors:  Hossein Fatemikia; Mohammad Seyedabadi; Zynab Karimi; Kiarash Tanha; Majid Assadi; Kaveh Tanha
Journal:  Mol Cell Biochem       Date:  2017-05-02       Impact factor: 3.396

4.  Matrix metalloproteinase-7 protects against acute kidney injury by priming renal tubules for survival and regeneration.

Authors:  Haiyan Fu; Dong Zhou; Haili Zhu; Jinlin Liao; Lin Lin; Xue Hong; Fan Fan Hou; Youhua Liu
Journal:  Kidney Int       Date:  2019-03-08       Impact factor: 10.612

5.  MicroRNA-150 deletion in mice protects kidney from myocardial infarction-induced acute kidney injury.

Authors:  Punithavathi Ranganathan; Calpurnia Jayakumar; Yaoping Tang; Kyoung-mi Park; Jian-peng Teoh; Huabo Su; Jie Li; Il-man Kim; Ganesan Ramesh
Journal:  Am J Physiol Renal Physiol       Date:  2015-06-24

6.  Cisplatin-Induced Non-Oliguric Acute Kidney Injury in a Pediatric Experimental Animal Model in Piglets.

Authors:  Maria José Santiago; Sarah Nicole Fernández; Alberto Lázaro; Rafael González; Javier Urbano; Jorge López; Maria José Solana; Blanca Toledo; Jimena Del Castillo; Alberto Tejedor; Jesús López-Herce
Journal:  PLoS One       Date:  2016-02-12       Impact factor: 3.240

Review 7.  Kidney disease models: tools to identify mechanisms and potential therapeutic targets.

Authors:  Yin-Wu Bao; Yuan Yuan; Jiang-Hua Chen; Wei-Qiang Lin
Journal:  Zool Res       Date:  2018-03-18

8.  The Impact of Versatile Macrophage Functions on Acute Kidney Injury and Its Outcomes.

Authors:  Jea-Hyun Baek
Journal:  Front Physiol       Date:  2019-08-06       Impact factor: 4.566

9.  A reduced form of nicotinamide riboside defines a new path for NAD+ biosynthesis and acts as an orally bioavailable NAD+ precursor.

Authors:  Judith Giroud-Gerbetant; Magali Joffraud; Maria Pilar Giner; Angelique Cercillieux; Simona Bartova; Mikhail V Makarov; Rubén Zapata-Pérez; José L Sánchez-García; Riekelt H Houtkooper; Marie E Migaud; Sofia Moco; Carles Canto
Journal:  Mol Metab       Date:  2019-10-03       Impact factor: 7.422

Review 10.  Group 2 Innate Lymphoid Cells Are Redundant in Experimental Renal Ischemia-Reperfusion Injury.

Authors:  Guy J M Cameron; Kelly M Cautivo; Svenja Loering; Simon H Jiang; Aniruddh V Deshpande; Paul S Foster; Andrew N J McKenzie; Ari B Molofsky; Philip M Hansbro; Malcolm R Starkey
Journal:  Front Immunol       Date:  2019-04-16       Impact factor: 7.561

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