Literature DB >> 26296948

Balancing the energy equation for healthy kidneys.

Peter F Mount1,2,3, David A Power1,2,3.   

Abstract

The high-energy requirement of the kidney and the importance of energy metabolism in renal physiology has been appreciated for decades, but only recently has there emerged a strong link between impaired renal energy metabolism and chronic kidney disease (CKD). The mechanisms underlying the association between changes in energy metabolism and progression of CKD, however, remain poorly understood. A new study from Qiu and colleagues reported in the Journal of Pathology has advanced this understanding by showing that, after renal injury, the energy sensor AMPK inhibits epithelial-mesenchymal transition and inflammation, processes important in the pathogenesis of CKD. Furthermore, this study identifies an interaction between AMPK and CK2β as an important mechanism in the anti-fibrotic effect. CK2β has previously been shown to interact with STK11 (also known as LKB1) to regulate cellular polarity. These findings are consistent with the known roles of the LKB1-AMPK pathway in sustaining cellular energy homeostasis and epithelial cell polarity, and add to growing evidence linking the suppression of energy metabolism to CKD. They emphasize the importance of energy metabolism in general and the LKB1-AMPK axis in particular as key investigational and therapeutic targets in the battle against CKD.
Copyright © 2015 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Entities:  

Keywords:  AMP-activated protein kinase (AMPK); chronic kidney disease (CKD); epithelial-mesenchymal transition (EMT); fatty acid oxidation (FAO); liver kinase B1 (LKB1/STK11); myofibroblast; tubulo-interstitial fibrosis (TIF)

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Year:  2015        PMID: 26296948     DOI: 10.1002/path.4600

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  7 in total

Review 1.  Pharmacologic Approaches to Improve Mitochondrial Function in AKI and CKD.

Authors:  Hazel H Szeto
Journal:  J Am Soc Nephrol       Date:  2017-08-04       Impact factor: 10.121

2.  Xanthine oxidase inhibitor ameliorates postischemic renal injury in mice by promoting resynthesis of adenine nucleotides.

Authors:  Kentaro Fujii; Akiko Kubo; Kazutoshi Miyashita; Masaaki Sato; Aika Hagiwara; Hiroyuki Inoue; Masaki Ryuzaki; Masanori Tamaki; Takako Hishiki; Noriyo Hayakawa; Yasuaki Kabe; Hiroshi Itoh; Makoto Suematsu
Journal:  JCI Insight       Date:  2019-11-14

Review 3.  New Pathogenic Concepts and Therapeutic Approaches to Oxidative Stress in Chronic Kidney Disease.

Authors:  José Pedraza-Chaverri; Laura G Sánchez-Lozada; Horacio Osorio-Alonso; Edilia Tapia; Alexandra Scholze
Journal:  Oxid Med Cell Longev       Date:  2016-06-27       Impact factor: 6.543

4.  Activation of PPARα by Oral Clofibrate Increases Renal Fatty Acid Oxidation in Developing Pigs.

Authors:  Yonghui He; Imad Khan; Xiumei Bai; Jack Odle; Lin Xi
Journal:  Int J Mol Sci       Date:  2017-12-08       Impact factor: 5.923

5.  Human Kidney Tubule-Specific Gene Expression Based Dissection of Chronic Kidney Disease Traits.

Authors:  Pazit Beckerman; Chengxiang Qiu; Jihwan Park; Nora Ledo; Yi-An Ko; Ae-Seo Deok Park; Sang-Youb Han; Peter Choi; Matthew Palmer; Katalin Susztak
Journal:  EBioMedicine       Date:  2017-09-18       Impact factor: 8.143

6.  Longitudinal changes in nutritional parameters and resting energy expenditure in end-stage renal disease.

Authors:  Mariana Cassani Oliveira; Marina Nogueira Berbel Bufarah; Daniela Ponce; André Balbi
Journal:  J Bras Nefrol       Date:  2019-10-24

Review 7.  The Role of Cardiolipin and Mitochondrial Damage in Kidney Transplant.

Authors:  Alejandra Guillermina Miranda-Díaz; Ernesto Germán Cardona-Muñoz; Fermín Paul Pacheco-Moisés
Journal:  Oxid Med Cell Longev       Date:  2019-11-25       Impact factor: 6.543

  7 in total

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