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Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney

The cyclooxygenase (COX) enzyme system is the major pathway catalyzing the conversion of arachidonic acid into prostaglandins (PGs). PGs are lipid mediators implicated in a variety of physiological and pathophysiological processes in the kidney, including renal hemodynamics, body water and sodium ba...

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Detalles Bibliográficos
Autores principales: Nørregaard, Rikke, Kwon, Tae-Hwan, Frøkiær, Jørgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688592/
https://www.ncbi.nlm.nih.gov/pubmed/26779421
http://dx.doi.org/10.1016/j.krcp.2015.10.004
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author Nørregaard, Rikke
Kwon, Tae-Hwan
Frøkiær, Jørgen
author_facet Nørregaard, Rikke
Kwon, Tae-Hwan
Frøkiær, Jørgen
author_sort Nørregaard, Rikke
collection PubMed
description The cyclooxygenase (COX) enzyme system is the major pathway catalyzing the conversion of arachidonic acid into prostaglandins (PGs). PGs are lipid mediators implicated in a variety of physiological and pathophysiological processes in the kidney, including renal hemodynamics, body water and sodium balance, and the inflammatory injury characteristic in multiple renal diseases. Since the beginning of 1990s, it has been confirmed that COX exists in 2 isoforms, referred to as COX-1 and COX-2. Even though the 2 enzymes are similar in size and structure, COX-1 and COX-2 are regulated by different systems and have different functional roles. This review summarizes the current data on renal expression of the 2 COX isoforms and highlights mainly the role of COX-2 and PGE2 in several physiological and pathophysiological processes in the kidney.
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spelling pubmed-46885922016-01-15 Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney Nørregaard, Rikke Kwon, Tae-Hwan Frøkiær, Jørgen Kidney Res Clin Pract Review Article The cyclooxygenase (COX) enzyme system is the major pathway catalyzing the conversion of arachidonic acid into prostaglandins (PGs). PGs are lipid mediators implicated in a variety of physiological and pathophysiological processes in the kidney, including renal hemodynamics, body water and sodium balance, and the inflammatory injury characteristic in multiple renal diseases. Since the beginning of 1990s, it has been confirmed that COX exists in 2 isoforms, referred to as COX-1 and COX-2. Even though the 2 enzymes are similar in size and structure, COX-1 and COX-2 are regulated by different systems and have different functional roles. This review summarizes the current data on renal expression of the 2 COX isoforms and highlights mainly the role of COX-2 and PGE2 in several physiological and pathophysiological processes in the kidney. Elsevier 2015-12 2015-11-12 /pmc/articles/PMC4688592/ /pubmed/26779421 http://dx.doi.org/10.1016/j.krcp.2015.10.004 Text en Copyright © 2015. The Korean Society of Nephrology. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Nørregaard, Rikke
Kwon, Tae-Hwan
Frøkiær, Jørgen
Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney
title Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney
title_full Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney
title_fullStr Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney
title_full_unstemmed Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney
title_short Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney
title_sort physiology and pathophysiology of cyclooxygenase-2 and prostaglandin e2 in the kidney
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688592/
https://www.ncbi.nlm.nih.gov/pubmed/26779421
http://dx.doi.org/10.1016/j.krcp.2015.10.004
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