Soluble Guanylate Cyclase as an Emerging Therapeutic Target in Cardiopulmonary Disease

被引:458
|
作者
Stasch, Johannes-Peter [2 ,3 ]
Pacher, Pal [4 ]
Evgenov, Oleg V. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Anesthesia Crit Care & Pain Med, Boston, MA 02114 USA
[2] Univ Halle Wittenberg, Inst Pharm, Halle, Germany
[3] Bayer HealthCare, Cardiol Res, Wuppertal, Germany
[4] NIAAA, Lab Physiol Studies, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
cardiovascular diseases; hypertension; pulmonary; nitric oxide; riociguat; soluble guanylate cyclase; PULMONARY ARTERIAL-HYPERTENSION; SYSTEMIC VASODILATOR RESPONSES; NO-INDEPENDENT STIMULATORS; MUSCLE-CELL-PROLIFERATION; NITRIC-OXIDE RECEPTOR; CYCLIC-GMP; BAY; 41-2272; SGC STIMULATOR; HEART-FAILURE; ENDOTHELIAL DYSFUNCTION;
D O I
10.1161/CIRCULATIONAHA.110.981738
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The concept of sGC stimulation as a treatment for cardiopulmonary disease has developed rapidly since its inception in the mid-1990s, and preclinical studies continue to shed new light on the properties of this drug class in a wide range of cardiopulmonary diseases (Figure 3). Riociguat, the first sGC stimulator to enter clinical development, has shown promising phase II results in CTEPH, PAH, and PH associated with interstitial lung disease and chronic obstructive pulmonary disease, whereas a phase II study of BAY 60-4552 has suggested that sGC stimulation may also have potential as a treatment for PH associated with biventricular heart failure. The ongoing phase III randomized controlled trials of riociguat in CTEPH and PAH are the first of many clinical studies of sGC stimulators. If successful, these studies will herald a new generation of treatments for cardiopulmonary disease. © 2011 American Heart Association, Inc.
引用
收藏
页码:2263 / 2273
页数:11
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