Eicosanoids, prostacyclin and cyclooxygenase in the cardiovascular system.


Journal

British journal of pharmacology
ISSN: 1476-5381
Titre abrégé: Br J Pharmacol
Pays: England
ID NLM: 7502536

Informations de publication

Date de publication:
04 2019
Historique:
received: 08 12 2017
revised: 19 01 2018
accepted: 29 01 2018
pubmed: 23 2 2018
medline: 4 7 2020
entrez: 23 2 2018
Statut: ppublish

Résumé

Eicosanoids represent a diverse family of lipid mediators with fundamental roles in physiology and disease. Within the eicosanoid superfamily are prostanoids, which are specifically derived from arachidonic acid by the enzyme cyclooxygenase (COX). COX has two isoforms; COX-1 and COX-2. COX-2 is the therapeutic target for the nonsteroidal anti-inflammatory drug (NSAID) class of pain medications. Of the prostanoids, prostacyclin, first discovered by Sir John Vane in 1976, remains amongst the best studied and retains an impressive pedigree as one of the fundamental cardiovascular protective pathways. Since this time, we have learnt much about how eicosanoids, COX enzymes and prostacyclin function in the cardiovascular system, knowledge that has allowed us, for example, to harness the power of prostacyclin as therapy to treat pulmonary arterial hypertension and peripheral vascular disease. However, there remain many unanswered questions in our basic understanding of the pathways, and how they can be used to improve human health. Perhaps, the most important and controversial outstanding question in the field remains; 'how do NSAIDs produce their much publicized cardiovascular side-effects?' This review summarizes the history, biology and cardiovascular function of key eicosanoids with particular focus on prostacyclin and other COX products and discusses how our knowledge of these pathways can applied in future drug discovery and be used to explain the cardiovascular side-effects of NSAIDs. LINKED ARTICLES: This article is part of a themed section on Eicosanoids 35 years from the 1982 Nobel: where are we now? To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.8/issuetoc.

Identifiants

pubmed: 29468666
doi: 10.1111/bph.14167
pmc: PMC6451069
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Eicosanoids 0
Epoprostenol DCR9Z582X0
Cyclooxygenase 1 EC 1.14.99.1
Cyclooxygenase 2 EC 1.14.99.1
PTGS1 protein, human EC 1.14.99.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1038-1050

Subventions

Organisme : British Heart Foundation
ID : FS/16/1/31699
Pays : United Kingdom

Informations de copyright

© 2018 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

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Auteurs

Jane A Mitchell (JA)

Cardiothoracic Pharmacology, National Heart and Lung Institute, London, UK.

Nicholas S Kirkby (NS)

Cardiothoracic Pharmacology, National Heart and Lung Institute, London, UK.

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Classifications MeSH