Imperial College London

ProfessorJaneMitchell

Faculty of MedicineNational Heart & Lung Institute

Professor of Pharmacology in Critical Care Medicine
 
 
 
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Contact

 

+44 (0)20 7351 8137j.a.mitchell

 
 
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Assistant

 

Ms Lisa Quinn +44 (0)20 7594 1345

 
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Location

 

Sir Alexander Fleming BuildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Mitchell:2019:10.1111/bph.14167,
author = {Mitchell, J and Kirkby, NS},
doi = {10.1111/bph.14167},
journal = {British Journal of Pharmacology},
pages = {1038--1050},
title = {Eicosanoids, prostacyclin and cyclooxygenase in the cardiovascular system},
url = {http://dx.doi.org/10.1111/bph.14167},
volume = {176},
year = {2019}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Eicosanoids represent a diverse family of lipid mediators with fundamental roles in controlling physiology and disease. Within the eicosanoid super family 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 Professor John Vane in 1976,remains amongst the best studied and retains an impressive pedigree as onethe bodies fundamental cardiovascular protective pathways. Since this time, we have learnt much about how eicosanoids, COXenzymes and prostacyclin function in the cardiovascular system which has allowed us to, for example, 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 usedto improve human health. Perhaps the most importantand controversial outstanding question in the field remains;‘how do NSAIDsproduce their much publicized cardiovascular side effects?’This review summarises the history, biology and cardiovascular function of key eicosanoids with particular focus on prostacyclin and other COXproducts 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.
AU - Mitchell,J
AU - Kirkby,NS
DO - 10.1111/bph.14167
EP - 1050
PY - 2019///
SN - 1476-5381
SP - 1038
TI - Eicosanoids, prostacyclin and cyclooxygenase in the cardiovascular system
T2 - British Journal of Pharmacology
UR - http://dx.doi.org/10.1111/bph.14167
UR - http://hdl.handle.net/10044/1/57233
VL - 176
ER -