Cyclooxygenase-1, not cyclooxygenase-2, is responsible for physiological production of prostacyclin in the cardiovascular system

被引:104
作者
Kirkby, Nicholas S. [1 ,2 ]
Lundberg, Martina H. [1 ,2 ]
Harrington, Louise S. [1 ]
Leadbeater, Philip D. M. [1 ]
Milne, Ginger L. [3 ,4 ]
Potter, Claire M. F. [1 ]
Al-Yamani, Malak [1 ,5 ]
Adeyemi, Oladipupo [1 ]
Warner, Timothy D. [2 ]
Mitchell, Jane A. [1 ,6 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, London SW3 6LY, England
[2] Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, London EC1M 6BQ, England
[3] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Med, Nashville, TN 37232 USA
[5] King Saud Univ, King Fahad Cardiac Ctr, Riyadh 11472, Saudi Arabia
[6] Inst Cardiovasc Med ICMS, London SW3 6NP, England
基金
英国惠康基金; 美国国家卫生研究院;
关键词
nonsteroidal anti-inflammatory drugs; thrombosis; COX-2 selective drugs; rofecoxib; NITRIC-OXIDE SYNTHASE; SHEAR-STRESS; PROSTAGLANDIN SYNTHASE; ANTIINFLAMMATORY DRUGS; VASCULAR ENDOTHELIUM; GENE-EXPRESSION; MESSENGER-RNA; COX ISOFORMS; INHIBITION; DISRUPTION;
D O I
10.1073/pnas.1209192109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prostacyclin is an antithrombotic hormone produced by the endothelium, whose production is dependent on cyclooxygenase (COX) enzymes of which two isoforms exist. It is widely believed that COX-2 drives prostacyclin production and that this explains the cardiovascular toxicity associated with COX-2 inhibition, yet the evidence for this relies on indirect evidence from urinary metabolites. Here we have used a range of experimental approaches to explore which isoform drives the production of prostacyclin in vitro and in vivo. Our data show unequivocally that under physiological conditions it is COX-1 and not COX-2 that drives prostacyclin production in the cardiovascular system, and that urinary metabolites do not reflect prostacyclin production in the systemic circulation. With the idea that COX-2 in endothelium drives prostacyclin production in healthy individuals removed, we must seek new answers to why COX-2 inhibitors increase the risk of cardiovascular events to move forward with drug discovery and to enable more informed prescribing advice.
引用
收藏
页码:17597 / 17602
页数:6
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