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Prostaglandins in the pathogenesis of kidney diseases
Prostaglandins (PGs) are important lipid mediators produced from arachidonic acid via the sequential catalyzation of cyclooxygenases (COXs) and specific prostaglandin synthases. There are five subtypes of PGs, namely PGE2, PGI2, PGD2, PGF2α, and thromboxane A2 (TXA2). PGs exert distinct roles by com...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995175/ https://www.ncbi.nlm.nih.gov/pubmed/29899878 http://dx.doi.org/10.18632/oncotarget.25005 |
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author | Li, Yuanyuan Xia, Weiwei Zhao, Fei Wen, Zhaoying Zhang, Aihua Huang, Songming Jia, Zhanjun Zhang, Yue |
author_facet | Li, Yuanyuan Xia, Weiwei Zhao, Fei Wen, Zhaoying Zhang, Aihua Huang, Songming Jia, Zhanjun Zhang, Yue |
author_sort | Li, Yuanyuan |
collection | PubMed |
description | Prostaglandins (PGs) are important lipid mediators produced from arachidonic acid via the sequential catalyzation of cyclooxygenases (COXs) and specific prostaglandin synthases. There are five subtypes of PGs, namely PGE2, PGI2, PGD2, PGF2α, and thromboxane A2 (TXA2). PGs exert distinct roles by combining to a diverse family of membrane-spanning G protein-coupled prostanoid receptors. The distribution of these PGs, their specific synthases and receptors vary a lot in the kidney. This review summarized the recent findings of PGs together with the COXs and their specific synthases and receptors in regulating renal function and highlighted the insights into their roles in the pathogenesis of various kidney diseases. |
format | Online Article Text |
id | pubmed-5995175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-59951752018-06-13 Prostaglandins in the pathogenesis of kidney diseases Li, Yuanyuan Xia, Weiwei Zhao, Fei Wen, Zhaoying Zhang, Aihua Huang, Songming Jia, Zhanjun Zhang, Yue Oncotarget Review Prostaglandins (PGs) are important lipid mediators produced from arachidonic acid via the sequential catalyzation of cyclooxygenases (COXs) and specific prostaglandin synthases. There are five subtypes of PGs, namely PGE2, PGI2, PGD2, PGF2α, and thromboxane A2 (TXA2). PGs exert distinct roles by combining to a diverse family of membrane-spanning G protein-coupled prostanoid receptors. The distribution of these PGs, their specific synthases and receptors vary a lot in the kidney. This review summarized the recent findings of PGs together with the COXs and their specific synthases and receptors in regulating renal function and highlighted the insights into their roles in the pathogenesis of various kidney diseases. Impact Journals LLC 2018-05-29 /pmc/articles/PMC5995175/ /pubmed/29899878 http://dx.doi.org/10.18632/oncotarget.25005 Text en Copyright: © 2018 Li et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Li, Yuanyuan Xia, Weiwei Zhao, Fei Wen, Zhaoying Zhang, Aihua Huang, Songming Jia, Zhanjun Zhang, Yue Prostaglandins in the pathogenesis of kidney diseases |
title | Prostaglandins in the pathogenesis of kidney diseases |
title_full | Prostaglandins in the pathogenesis of kidney diseases |
title_fullStr | Prostaglandins in the pathogenesis of kidney diseases |
title_full_unstemmed | Prostaglandins in the pathogenesis of kidney diseases |
title_short | Prostaglandins in the pathogenesis of kidney diseases |
title_sort | prostaglandins in the pathogenesis of kidney diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995175/ https://www.ncbi.nlm.nih.gov/pubmed/29899878 http://dx.doi.org/10.18632/oncotarget.25005 |
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