Soluble guanylate cyclase stimulator riociguat and phosphodiesterase 5 inhibitor sildenafil ameliorate pulmonary hypertension due to left heart disease in mice

被引:25
作者
Pradhan, Kabita [1 ]
Sydykov, Akylbek [1 ]
Tian, Xia [1 ]
Mamazhakypov, Argen [1 ]
Neupane, Balram [1 ]
Luitel, Himal [1 ]
Weissmann, Norbert [1 ]
Seeger, Werner [1 ,2 ]
Grimminger, Friedrich [1 ]
Kretschmer, Axel [3 ]
Stasch, Johannes-Peter [3 ]
Ghofrani, Hossein Ardeschir [1 ]
Schermuly, Ralph Theo [1 ]
机构
[1] Univ Giessen, Univ Giessen & Marburg Lung Ctr, Excellence Cluster Cardiopulm Syst, D-35390 Giessen, Germany
[2] Max Planck Inst Heart & Lung Res, Pk Str 1, D-61231 Bad Nauheim, Germany
[3] Bayer HealthCare, Aprather Weg 18a, D-42096 Wuppertal, Germany
关键词
Transverse aortic constriction; Riociguat; Sildenafil; Pulmonary hypertension; Heart failure; DIASTOLIC FUNCTION; CARDIAC FIBROSIS; PRESSURE; FAILURE; HYPERTROPHY; ACTIVATION;
D O I
10.1016/j.ijcard.2016.04.098
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Presence of pulmonary hypertension (PH) and right ventricular dysfunction worsens prognosis in patients with chronic heart failure (CHF). Preclinical and clinical studies suggest a role for the impaired nitric oxide (NO)-soluble guanylate cyclase (sGC)-cyclic guanosine monophosphate (cGMP) signaling pathway in both PH and CHF. Hence, we examined the effects of the NO-sGC-cGMP pathway modulation by the PDE5 inhibitor sildenafil or sGC stimulator riociguat on pulmonary hemodynamics and heart function in a murine model of secondary PH induced by transverse aortic constriction. Methods: C57Bl/6N mice were subjected to transverse aortic constriction (TAC) for 6 weeks to induce left heart failure and secondary PH and were subsequently treated with either sildenafil (100 mg/kg/day) or riociguat (10 mg/kg/day) or placebo for 2 weeks. Results: Six weeks after surgery, TAC induced significant left ventricular hypertrophy and dysfunction associated with development of PH. Treatment with riociguat and sildenafil neither reduced left ventricular hypertrophy nor improved its function. However, both sildenafil and riociguat ameliorated PH, reduced pulmonary vascular remodeling and improved right ventricular function. Conclusions: Thus, modulation of the NO-sGC-cGMP pathway by the PDE5 inhibitor sildenafil or sGC stimulator riociguat exerts direct beneficial effects on pulmonary hemodynamics and right ventricular function in the experimental model of secondary PH due to left heart disease and these drugs may offer a new therapeutic option for therapy of this condition. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:85 / 91
页数:7
相关论文
共 39 条
[1]   Protein Kinase G Iα Inhibits Pressure Overload-Induced Cardiac Remodeling and Is Required for the Cardioprotective Effect of Sildenafil In Vivo [J].
Blanton, Robert M. ;
Takimoto, Eiki ;
Lane, Angela M. ;
Aronovitz, Mark ;
Piotrowski, Robert ;
Karas, Richard H. ;
Kass, David A. ;
Mendelsohn, Michael E. .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2012, 1 (05) :e003731
[2]   Cardiorenal and humoral properties of a novel direct soluble guanylate cyclase stimulator BAY 41-2272 in experimental congestive heart failure [J].
Boerrigter, G ;
Costello-Boerrigter, LC ;
Cataliotti, A ;
Tsuruda, T ;
Harty, GJ ;
Lapp, H ;
Stasch, JP ;
Burnett, JC .
CIRCULATION, 2003, 107 (05) :686-689
[3]   Sildenafil treatment in established right ventricular dysfunction improves diastolic function and attenuates interstitial fibrosis independent from afterload [J].
Borgdorff, Marinus A. ;
Bartelds, Beatrijs ;
Dickinson, Michael G. ;
van Wiechen, Maarten P. H. ;
Steendijk, Paul ;
de Vroomen, Maartje ;
Berger, Rolf M. F. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2014, 307 (03) :H361-H369
[4]   Left Ventricular Failure Produces Profound Lung Remodeling and Pulmonary Hypertension in Mice Heart Failure Causes Severe Lung Disease [J].
Chen, Yingjie ;
Guo, Haipeng ;
Xu, Dachun ;
Xu, Xin ;
Wang, Huan ;
Hu, Xinli ;
Lu, Zhongbing ;
Kwak, Dongmin ;
Xu, Yawei ;
Gunther, Roland ;
Huo, Yuqing ;
Weir, E. Kenneth .
HYPERTENSION, 2012, 59 (06) :1170-U239
[5]   Reduction of cardiac fibrosis decreases systolic performance without affecting diastolic function in hypertensive rats [J].
Cingolani, OH ;
Yang, XP ;
Liu, YH ;
Villanueva, M ;
Rhaleb, NE ;
Carretero, OA .
HYPERTENSION, 2004, 43 (05) :1067-1073
[6]   Pulmonary hypertension in left heart disease: A review [J].
Corte, Tamera J. ;
McDonagh, Theresa A. ;
Wort, Stephen J. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2012, 156 (03) :253-258
[7]  
de Almeida A.C., 2010, J VIS EXP
[8]   Activation of soluble guanylate cyclase reverses experimental pulmonary hypertension and vascular remodeling [J].
Dumitrascu, R ;
Weissmann, N ;
Ghofrani, HA ;
Dony, E ;
Beuerlein, K ;
Schmidt, H ;
Stasch, JP ;
Gnoth, MJ ;
Seeger, W ;
Grimminger, F ;
Schermuly, RT .
CIRCULATION, 2006, 113 (02) :286-295
[9]   Soluble guanylyl cyclase activation improves progressive cardiac remodeling and failure after myocardial infarction. Cardioprotection over ACE inhibition [J].
Fraccarollo, Daniela ;
Galuppo, Paolo ;
Motschenbacher, Stephanie ;
Ruetten, Hartmut ;
Schaefer, Andreas ;
Bauersachs, Johann .
BASIC RESEARCH IN CARDIOLOGY, 2014, 109 (04)
[10]   Soluble Guanylate Cyclase Stimulation Prevents Fibrotic Tissue Remodeling and Improves Survival in Salt-Sensitive Dahl Rats [J].
Geschka, Sandra ;
Kretschmer, Axel ;
Sharkovska, Yuliya ;
Evgenov, Oleg V. ;
Lawrenz, Bettina ;
Hucke, Andreas ;
Hocher, Berthold ;
Stasch, Johannes-Peter .
PLOS ONE, 2011, 6 (07)