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利奥西呱、西地那非和吸入一氧化氮可降低急性肺栓塞猪模型的肺血管阻力并改善右心室功能。

Riociguat, sildenafil and inhaled nitric oxide reduces pulmonary vascular resistance and improves right ventricular function in a porcine model of acute pulmonary embolism.

机构信息

Department of Cardiology, Aarhus University Hospital, Denmark.

Department of Clinical Medicine, Faculty of Health, Aarhus University, Denmark.

出版信息

Eur Heart J Acute Cardiovasc Care. 2020 Jun;9(4):293-301. doi: 10.1177/2048872619840772. Epub 2019 Apr 26.

Abstract

BACKGROUND

Pulmonary vasodilators as add-on to current treatment strategies in acute pulmonary embolism may improve right ventricular unloading and hence improve patient outcome. We aimed to investigate whether stimulation of the nitric oxide (NO)-soluble guanylate cyclase (sGC)-cyclic guanosine monophosphate (cGMP) pathway with riociguat, sildenafil or inhaled NO causes pulmonary vasodilation and improves right ventricular function in a porcine model of acute intermediate risk pulmonary embolism.

METHODS

Two large autologous blood clots were administered to the pulmonary circulation of 28 pigs (60 kg). Animals were randomized to four increasing, clinically equivalent doses of riociguat (=6), sildenafil (=6), inhaled NO (=6) or vehicle (=6). Sham animals (=4) did not receive pulmonary embolism or treatment. Haemodynamic responses were evaluated at baseline, after pulmonary embolism and after each dose using invasive pressure measurements, transoesophageal echocardiography, respiratory parameters and blood analysis.

RESULTS

Pulmonary embolism caused a three-fold increase in pulmonary vascular resistance compared with baseline (pulmonary embolism: 352±29 . baseline: 107±6 dynes, <0.0001). All treatments lowered pulmonary vascular resistance compared with vehicle (riociguat: -158±35, sildenafil: -224±35, inhaled NO: -156±35 dynes, <0.0001). Sildenafil, but neither inhaled NO nor riociguat, caused a decrease in systemic vascular resistance (sildenafil 678±41 . vehicle 1081±93 dynes, =0.02) and increased cardiac output (sildenafil 8.8±0.8 . vehicle: 5.9±0.2 L/min, <0.001). Systemic blood pressure was unaltered in all treatment groups.

CONCLUSION

Stimulation of the NO-sGC-cGMP pathway by riociguat, sildenafil and inhaled NO reduces pulmonary vascular resistance in a porcine model of acute pulmonary embolism without lowering systemic blood pressure.

摘要

背景

在急性肺栓塞中,将肺动脉扩张剂作为现有治疗策略的附加手段,可以改善右心室的卸载,从而改善患者的预后。我们旨在研究在急性中度风险肺栓塞的猪模型中,使用利奥西呱、西地那非或吸入一氧化氮(NO)刺激一氧化氮(NO)-可溶性鸟苷酸环化酶(sGC)-环鸟苷单磷酸(cGMP)途径是否会引起肺血管舒张并改善右心室功能。

方法

将 28 头(60 公斤)猪的 2 个大自体血凝块注入肺循环。动物随机分为 4 组,分别接受递增的、临床等效剂量的利奥西呱(=6)、西地那非(=6)、吸入的 NO(=6)或载体(=6)。假手术组(=4)未接受肺栓塞或治疗。使用有创压力测量、经食管超声心动图、呼吸参数和血液分析,在基线、肺栓塞后和每次剂量后评估血流动力学反应。

结果

与基线相比,肺栓塞使肺血管阻力增加了三倍(肺栓塞:352±29 dynes,基线:107±6 dynes,<0.0001)。与载体相比,所有治疗方法均降低了肺血管阻力(利奥西呱:-158±35,西地那非:-224±35,吸入的 NO:-156±35 dynes,<0.0001)。西地那非,而不是吸入的 NO 或利奥西呱,降低了全身血管阻力(西地那非 678±41 dynes,载体 1081±93 dynes,=0.02)并增加了心输出量(西地那非 8.8±0.8 L/min,载体:5.9±0.2 L/min,<0.001)。所有治疗组的全身血压均未改变。

结论

在急性肺栓塞的猪模型中,NO-sGC-cGMP 途径的刺激通过利奥西呱、西地那非和吸入的 NO 降低肺血管阻力,而不降低全身血压。

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