University of Giessen and Marburg Lung Center, Giessen, Germany.
PLoS One. 2012;7(8):e43433. doi: 10.1371/journal.pone.0043433. Epub 2012 Aug 17.
The nitric oxide (NO)-soluble guanylate cyclase (sGC)-cyclic guanosine monophosphate (cGMP) signal-transduction pathway is impaired in many cardiovascular diseases, including pulmonary arterial hypertension (PAH). Riociguat (BAY 63-2521) is a stimulator of sGC that works both in synergy with and independently of NO to increase levels of cGMP. The aims of this study were to investigate the role of NO-sGC-cGMP signaling in a model of severe PAH and to evaluate the effects of sGC stimulation by riociguat and PDE5 inhibition by sildenafil on pulmonary hemodynamics and vascular remodeling in severe experimental PAH.
Severe angioproliferative PAH was induced in rats by combined exposure to the vascular endothelial growth factor receptor antagonist SU5416 and hypoxia (SUHx). Twenty-one days thereafter rats were randomized to receive either riociguat (10 mg/kg/day), sildenafil (50 mg/kg/day) or vehicle by oral gavage, for 14 days until the day of the terminal hemodynamic measurements. Administration of riociguat or sildenafil significantly decreased right ventricular systolic pressure (RVSP). Riociguat significantly decreased RV hypertrophy (RVH) (0.55 ± 0.02, p<0.05), increased cardiac output (60.8 ± .8 mL/minute, p<0.05) and decreased total pulmonary resistance (4.03 ± 0.3 mmHg min(-1) ml(-1) 100 g BW, p<0.05), compared with sildenafil and vehicle. Both compounds significantly decreased the RV collagen content and improved RV function, but the effects of riociguat on tricuspid annular plane systolic excursion and RV myocardial performance were significantly better than those of sildenafil (p<0.05). The proportion of occluded arteries was significantly lower in animals receiving riociguat than in those receiving vehicle (p<0.05); furthermore, the neointima/media ratio was significantly lower in those receiving riociguat than in those receiving sildenafil or vehicle (p<0.05).
Riociguat and sildenafil significantly reduced RVSP and RVH, and improved RV function compared with vehicle. Riociguat had a greater effect on hemodynamics and RVH than sildenafil.
一氧化氮(NO)-可溶性鸟苷酸环化酶(sGC)-环鸟苷酸(cGMP)信号转导通路在许多心血管疾病中受损,包括肺动脉高压(PAH)。利奥西呱(BAY 63-2521)是 sGC 的激动剂,它与 NO 协同作用并独立于 NO 发挥作用,增加 cGMP 的水平。本研究旨在探讨 NO-sGC-cGMP 信号在严重 PAH 模型中的作用,并评估 sGC 刺激利奥西呱和 PDE5 抑制西地那非对严重实验性 PAH 的肺血流动力学和血管重塑的影响。
通过联合暴露于血管内皮生长因子受体拮抗剂 SU5416 和缺氧(SUHx)在大鼠中诱导严重的血管增殖性 PAH。21 天后,大鼠随机接受利奥西呱(10 mg/kg/天)、西地那非(50 mg/kg/天)或载体口服灌胃,持续 14 天,直至进行终末血流动力学测量的那一天。利奥西呱或西地那非的给药显著降低右心室收缩压(RVSP)。利奥西呱显著降低 RV 肥厚(RVH)(0.55 ± 0.02,p<0.05),增加心输出量(60.8 ±.8 毫升/分钟,p<0.05)并降低总肺阻力(4.03 ± 0.3 mmHg min(-1) ml(-1) 100 g BW,p<0.05),与西地那非和载体相比。两种化合物均显著降低 RV 胶原含量并改善 RV 功能,但利奥西呱对三尖瓣环平面收缩期位移和 RV 心肌性能的影响明显优于西地那非(p<0.05)。接受利奥西呱治疗的动物中闭塞动脉的比例明显低于接受载体治疗的动物(p<0.05);此外,接受利奥西呱治疗的动物的新生内膜/中膜比值明显低于接受西地那非或载体治疗的动物(p<0.05)。
与载体相比,利奥西呱和西地那非显著降低 RVSP 和 RVH,并改善 RV 功能。与西地那非相比,利奥西呱对血流动力学和 RVH 的影响更大。