Hsu Henry H, Rubin Lewis J
CoTherix, Inc., 5000 Shoreline Court, San Francisco, CA 94080, USA.
Expert Opin Pharmacother. 2005 Sep;6(11):1921-30. doi: 10.1517/14656566.6.11.1921.
Pulmonary arterial hypertension (PAH) is a condition that is characterised by increased pulmonary arterial pressure and vascular resistance that can lead to right ventricular failure and death. A variety of disturbances in pulmonary vascular endothelial and smooth muscle function are present in PAH, including reduced production of vasodilator and antiproliferative substances, such as nitric oxide and prostacyclin, and an overproduction of mitogens, such as endothelin. As a result of these observations, therapies have been developed for PAH that specifically target these pathogenic processes, including prostacyclin analogues and endothelin receptor antagonists. This article reviews iloprost inhalation solution, the most recently approved form of prostacyclin therapy that is delivered directly to the lungs by inhalation.
肺动脉高压(PAH)是一种以肺动脉压力升高和血管阻力增加为特征的疾病,可导致右心室衰竭和死亡。PAH存在多种肺血管内皮和平滑肌功能紊乱,包括血管舒张剂和抗增殖物质(如一氧化氮和前列环素)生成减少,以及有丝分裂原(如内皮素)生成过多。基于这些观察结果,已开发出针对PAH的疗法,这些疗法专门针对这些致病过程,包括前列环素类似物和内皮素受体拮抗剂。本文综述了吸入用伊洛前列素溶液,这是最近获批的通过吸入直接送达肺部的前列环素治疗药物。