Celecoxib activates PI-3K/Akt and mitochondrial redox signaling to enhance heme oxygenase-1-mediated anti-inflammatory activity in vascular endothelium

被引:73
作者
Hamdulay, Shahir S. [1 ]
Wang, Bufei [1 ]
Birdsey, Graeme M. [1 ]
Ali, Faisal [1 ]
Dumont, Odile [1 ]
Evans, Paul C. [1 ]
Haskard, Dorian O. [1 ]
Wheeler-Jones, Caroline P. [2 ]
Mason, Justin C. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Bywaters Ctr Vasc Inflammat, Natl Heart & Lung Inst, London W12 0NN, England
[2] Univ London Royal Vet Coll, Dept Vet Basic Sci, London, England
关键词
Heme oxygenase-1; Endothelial cells; Inflammation; Redox signaling; Reactive oxygen species; Celecoxib; Cytoprotection; Free radicals; CORONARY-ARTERY-DISEASE; COX-2; INHIBITORS; CARDIOVASCULAR RISK; CYCLOOXYGENASE-2; RHEUMATOID-ARTHRITIS; OXIDATIVE DAMAGE; PROTEIN-KINASE; CELLS; DRUGS; EXPRESSION;
D O I
10.1016/j.freeradbiomed.2010.01.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although nonsteroidal anti-inflammatory drugs (NSAIDs) provide important control of pain and inflammation, they have been overshadowed by concerns regarding atherothrombotic complications However, celecoxib seems to have a relatively good cardiovascular profile and may improve endothelial function in coronary heart disease This led us to the hypothesis that celecoxib induces the vasculoprotective enzyme home oxygenase-1 (HO-1) In human umbilical vein and aortic endothelial cells. 24-48 h treatment with celecoxib induced HO-1 mRNA and protein expression and increased HO-1 enzyme activity This effect was not seen with rofecoxib or indomethacin Supplementation of culture medium with iloprost or prostaglandin E-2 failed to reverse celecoxib-mediated HO-1 induction, indicating a cyclooxygenase-independent mechanism Rather, this action of celecoxib involved generation of mitochondria-derived reactive oxygen species. Akt phosphorylation. and nuclear translocation of the transcription factor Nrf2, with N-acetylcysteine. PI-3K antagonist LY290042. and dominant-negative Akt abrogating the effects Furthermore, celecoxib-induced HO-1 was inhibited by dominant-negative Nrf2 The functional significance of HO-1 induction was revealed by celecoxib-mediated inhibition of VCAM-I expression, a response reversed by the HO-1 antagonist zinc protoporphyrin HO-1 induction provides a molecular mechanism for clinical observations indicating relative freedom from atherothrombotic complications in patients taking celecoxib compared to other NSAIDs with comparable anti-inflammatory activity (C) 2010 Elsevier Inc All rights reserved
引用
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页码:1013 / 1023
页数:11
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