Preston Ioana R
Pulmonary, Critical Care and Sleep Division, Tufts-New England Medical Center, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Antioxid Redox Signal. 2007 Jun;9(6):711-21. doi: 10.1089/ars.2007.1587.
Pulmonary hypertension is a condition associated with a variety of pulmonary disorders whose common denominator is alveolar hypoxia. Such disorders include chronic obstructive pulmonary disease, pulmonary fibrosis, sleep-disordered breathing, and exposure to high altitude. Acute hypoxia is characterized by vasoconstriction of small pulmonary arteries, a phenomenon called hypoxic pulmonary vasoconstriction. With prolonged hypoxia, thickening of the smooth vascular layer of the small pulmonary arteries occurs, a phenomenon described as pulmonary vascular remodeling. Although the core mechanisms of both vasoconstriction and remodeling are thought to reside in the smooth muscle cell layer, the endothelium modulates these two processes. The purpose of this review is briefly to (a) discuss the mechanisms of hypoxic pulmonary hypertension as it pertains to certain disease states, and (b) examine the pathways that have potential therapeutic applications for this condition.
肺动脉高压是一种与多种肺部疾病相关的病症,其共同特征是肺泡缺氧。这些疾病包括慢性阻塞性肺疾病、肺纤维化、睡眠呼吸障碍以及高原暴露。急性缺氧的特征是肺小动脉血管收缩,这一现象称为缺氧性肺血管收缩。随着缺氧时间延长,肺小动脉血管平滑肌层会增厚,这一现象被描述为肺血管重塑。尽管血管收缩和重塑的核心机制被认为存在于平滑肌细胞层,但内皮细胞会调节这两个过程。本综述的目的是简要地(a)讨论与某些疾病状态相关的缺氧性肺动脉高压的机制,以及(b)研究对这种病症具有潜在治疗应用价值的途径。