Cardioprotection with phosphodiesterase-5 inhibition - a novel preconditioning strategy

被引:125
作者
Kukreja, RC [1 ]
Ockaili, R [1 ]
Salloum, F [1 ]
Yin, C [1 ]
Hawkins, J [1 ]
Das, A [1 ]
Xi, L [1 ]
机构
[1] Virginia Commonwealth Univ, Ctr Med, Div Cardiol, Dept Internal Med, Richmond, VA 23298 USA
关键词
phosphodiesterase inhibitors; myocardial preconditioning; ischemia-reperfusion injury; vasodilatation; pulmonary hypertension; endothelial dysfunction; nitric oxide; cGMP; potassium channel; protein kinase;
D O I
10.1016/j.yjmcc.2003.11.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Phosphodiesterase type-5 (PDE-5) inhibitors including sildenafil, vardenafil and tadalafil are a new class of vasoactive drugs that have been developed for treatment of erectile dysfunction in patients. A growing number of studies in recent years suggest that sildenafil may be used clinically for treatment of pulmonary hypertension and endothelial dysfunction. In addition, recent studies primarily from our laboratory suggested that sildenafil has preconditioning-like powerful cardioprotective effect in the animal models of ischemia-reperfusion injury. Sildenafil has been found to exert cardioprotection through nitric oxide generated from endothelial and/or inducible nitric oxide synthases and opening of mitochondrial ATP-sensitive potassium channels. Future demonstration of the cardioprotective effect in patients with the relatively safe and effective FDA-approved PDE-5 inhibitors, such as sildenafil, could have an enormous impact on bringing the long-studied phenomena of ischemic and pharmacologic preconditioning to the clinical forefront. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:165 / 173
页数:9
相关论文
共 75 条
[41]   Role of p38 mitogen-activated protein kinases in preconditioning - A detrimental factor or a protective kinase? [J].
Ping, PP ;
Murphy, E .
CIRCULATION RESEARCH, 2000, 86 (09) :921-922
[42]   Ischemic preconditioning induces selective translocation of protein kinase C isoforms epsilon and eta in the heart of conscious rabbits without subcellular redistribution of total protein kinase C activity [J].
Ping, PP ;
Zhang, J ;
Qiu, YM ;
Tang, XL ;
Manchikalapudi, S ;
Cao, XN ;
Bolli, R .
CIRCULATION RESEARCH, 1997, 81 (03) :404-414
[43]   The efficacy and tolerability of vardenafil, a new, oral, selective phosphodiesterase type 5 inhibitor, in patients with erectile dysfunction: the first at-home clinical trial [J].
Porst, H ;
Rosen, R ;
Padma-Nathan, H ;
Goldstein, I ;
Giuliano, F ;
Ulbrich, E ;
Bandel, T .
INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2001, 13 (04) :192-199
[44]   Sustained activation of p42/p44 mitogen-activated protein kinase during recovery from simulated ischaemia mediates adaptive cytoprotection in cardiomyocytes [J].
Punn, A ;
Mockridge, JW ;
Farooqui, S ;
Marber, MS ;
Heads, RJ .
BIOCHEMICAL JOURNAL, 2000, 350 :891-899
[45]   Effects of sildenafil on myocardial infarct size, microvascular function, and acute ischemic left ventricular dilation [J].
Reffelmann, T ;
Kloner, RA .
CARDIOVASCULAR RESEARCH, 2003, 59 (02) :441-449
[46]   Phosphodiesterase 5 inhibitors: Current status and potential applications [J].
Rotella, DP .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (09) :674-682
[47]  
Salloum F, 2002, CIRCULATION, V106, P378
[48]   Sildenafil induces delayed preconditioning through inducible nitric oxide synthase-dependent pathway in mouse heart [J].
Salloum, F ;
Yin, C ;
Xi, L ;
Kukreja, RC .
CIRCULATION RESEARCH, 2003, 92 (06) :595-597
[49]   Activation of mitochondrial ATP-dependent potassium channels by nitric oxide [J].
Sasaki, N ;
Sato, T ;
Ohler, A ;
O'Rourke, B ;
Marbán, E .
CIRCULATION, 2000, 101 (04) :439-445
[50]   Ischemic preconditioning in the intact rat heart is mediated by δ1- but not μ- or κ-opioid receptors [J].
Schultz, JE ;
Hsu, AK ;
Gross, GJ .
CIRCULATION, 1998, 97 (13) :1282-1289