Targeting Nrf2 in Protection Against Renal Disease

Renal disease is a serious health problem, with increasing incidence and prevalence. Oxidative stress and inflammation play a key role in the pathogenesis and progression of renal disease. Therefore, therapeutic approaches to decrease oxidative stress should be of interest. This review aims to provi...

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Published in:Current medicinal chemistry Vol. 24; no. 33; p. 3583
Main Authors: Guerrero-Hue, Melania, Farre-Alins, Victor, Palomino-Antolin, Alejandra, Parada, Esther, Rubio-Navarro, Alfonso, Egido, Jesus, Egea, Javier, Moreno, Juan A
Format: Journal Article
Language:English
Published: Netherlands 01-01-2017
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Abstract Renal disease is a serious health problem, with increasing incidence and prevalence. Oxidative stress and inflammation play a key role in the pathogenesis and progression of renal disease. Therefore, therapeutic approaches to decrease oxidative stress should be of interest. This review aims to provide a comprehensive and updated overview of the protective mechanisms mediated by Nrf2 (nuclear factor erythroid 2-related factor 2), a description of novel compounds that target Nrf2, its effectiveness to prevent renal disease and the on-going clinical trials for this pathological condition. We undertook a structured search of bibliographic databases for peer-reviewed research in literature about Nrf2 activators and renal disease. The transcription factor Nrf2 is an emerging regulator of cellular resistance to oxidants and inflammation. Nrf2 controls the basal and induced expression of a couple of cytoprotective and antiinflammatory genes that regulate the physiological and pathophysiological outcomes of oxidant exposure. We have analyzed numerous findings showing that Nrf2 induction protects against oxidative stress and modulates inflammation in acute kidney injury and chronic kidney disease progression. However, few clinical trials have been performed in humans. Recent studies suggested that renoprotective effects of Nrf2 activation are observed at low doses, whereas harmful effects appear at higher concentrations. The findings of this review confirm that novel studies are necessary to address whether Nrf2-targeting may be a safe therapeutic approach to decrease renal disease progression in humans.
AbstractList Renal disease is a serious health problem, with increasing incidence and prevalence. Oxidative stress and inflammation play a key role in the pathogenesis and progression of renal disease. Therefore, therapeutic approaches to decrease oxidative stress should be of interest. This review aims to provide a comprehensive and updated overview of the protective mechanisms mediated by Nrf2 (nuclear factor erythroid 2-related factor 2), a description of novel compounds that target Nrf2, its effectiveness to prevent renal disease and the on-going clinical trials for this pathological condition. We undertook a structured search of bibliographic databases for peer-reviewed research in literature about Nrf2 activators and renal disease. The transcription factor Nrf2 is an emerging regulator of cellular resistance to oxidants and inflammation. Nrf2 controls the basal and induced expression of a couple of cytoprotective and antiinflammatory genes that regulate the physiological and pathophysiological outcomes of oxidant exposure. We have analyzed numerous findings showing that Nrf2 induction protects against oxidative stress and modulates inflammation in acute kidney injury and chronic kidney disease progression. However, few clinical trials have been performed in humans. Recent studies suggested that renoprotective effects of Nrf2 activation are observed at low doses, whereas harmful effects appear at higher concentrations. The findings of this review confirm that novel studies are necessary to address whether Nrf2-targeting may be a safe therapeutic approach to decrease renal disease progression in humans.
Author Egido, Jesus
Egea, Javier
Palomino-Antolin, Alejandra
Rubio-Navarro, Alfonso
Moreno, Juan A
Parada, Esther
Guerrero-Hue, Melania
Farre-Alins, Victor
Author_xml – sequence: 1
  givenname: Melania
  surname: Guerrero-Hue
  fullname: Guerrero-Hue, Melania
  organization: Renal, Vascular and Diabetes Research Laboratory, Instituto de Investigacion Sanitaria -Fundacion Jimenez Diaz, Autonoma University, 28040 Madrid. Spain
– sequence: 2
  givenname: Victor
  surname: Farre-Alins
  fullname: Farre-Alins, Victor
  organization: Instituto de Investigacion Sanitaria-Hospital Universitario de la Princesa, Madrid, Spain; Department of Pharmacology, Instituto Teofilo Hernando, Facultad de Medicina, UAM, Madrid. Spain
– sequence: 3
  givenname: Alejandra
  surname: Palomino-Antolin
  fullname: Palomino-Antolin, Alejandra
  organization: Instituto de Investigacion Sanitaria-Hospital Universitario de la Princesa, Madrid, Spain; Department of Pharmacology, Instituto Teofilo Hernando, Facultad de Medicina, UAM, Madrid. Spain
– sequence: 4
  givenname: Esther
  surname: Parada
  fullname: Parada, Esther
  organization: Instituto de Investigacion Sanitaria-Hospital Universitario de la Princesa, Madrid, Spain; Department of Pharmacology, Instituto Teofilo Hernando, Facultad de Medicina, UAM, Madrid. Spain
– sequence: 5
  givenname: Alfonso
  surname: Rubio-Navarro
  fullname: Rubio-Navarro, Alfonso
  organization: Renal, Vascular and Diabetes Research Laboratory, Instituto de Investigacion Sanitaria -Fundacion Jimenez Diaz, Autonoma University, 28040 Madrid. Spain
– sequence: 6
  givenname: Jesus
  surname: Egido
  fullname: Egido, Jesus
  organization: Renal, Vascular and Diabetes Research Laboratory, Instituto de Investigacion Sanitaria -Fundacion Jimenez Diaz, Autonoma University, 28040 Madrid. Spain
– sequence: 7
  givenname: Javier
  surname: Egea
  fullname: Egea, Javier
  organization: Instituto de Investigacion Sanitaria, Servicio de Farmacologia Clinica, Hospital Universitario de la Princesa, Madrid, Spain; Instituto Teofilo Hernando, Department of Pharmacology, Universidad Autonoma de Madrid, C/Arzobispo Morcillo 4, 28029 Madrid. Spain
– sequence: 8
  givenname: Juan A
  surname: Moreno
  fullname: Moreno, Juan A
  organization: Renal, Vascular and Diabetes Research Laboratory. IIS-Fundacion Jimenez Diaz. Av. Reyes Catolicos 2, 28040-Madrid. Spain
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Keywords oxidation
acute and chronic kidney injury
Nrf2
inflammation
therapy
renal damage
Language English
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Snippet Renal disease is a serious health problem, with increasing incidence and prevalence. Oxidative stress and inflammation play a key role in the pathogenesis and...
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StartPage 3583
SubjectTerms Acute Kidney Injury - drug therapy
Acute Kidney Injury - genetics
Acute Kidney Injury - metabolism
Acute Kidney Injury - pathology
Animals
Drug Discovery
Gene Expression Regulation - drug effects
Humans
Inflammation - drug therapy
Inflammation - genetics
Inflammation - metabolism
Inflammation - pathology
Kidney - drug effects
Kidney - metabolism
Kidney - pathology
Molecular Targeted Therapy
NF-E2-Related Factor 2 - agonists
NF-E2-Related Factor 2 - genetics
NF-E2-Related Factor 2 - metabolism
Oxidative Stress - drug effects
Renal Insufficiency, Chronic - drug therapy
Renal Insufficiency, Chronic - genetics
Renal Insufficiency, Chronic - metabolism
Renal Insufficiency, Chronic - pathology
Signal Transduction - drug effects
Title Targeting Nrf2 in Protection Against Renal Disease
URI https://www.ncbi.nlm.nih.gov/pubmed/28494744
Volume 24
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