Steinhorn R H, Morin F C, Fineman J R
Department of Pediatrics and Physiology, State University of New York at Buffalo, USA.
Semin Perinatol. 1997 Oct;21(5):393-408. doi: 10.1016/s0146-0005(97)80005-5.
At birth, a marked decrease in pulmonary vascular resistance allows the lung to establish gas exchange. Persistent pulmonary hypertension of the newborn (PPHN) occurs when this normal adaptation of gas exchange does not occur. We review animal models used to study the pathogenesis and treatment of PPHN. Both acute models, such as acute hypoxia and infusion of vasoconstrictors, and chronic models of PPHN created both before and immediately after birth are described. Inhaled nitric oxide is an important emerging therapy for PPHN. We review nitric oxide receptor mechanisms, including soluble guanylate cyclase, which produces cGMP when stimulated by nitric oxide, and phosphodiesterases, which control the intensity and duration of cGMP signal transduction. A better understanding of these mechanisms of regulation of vascular tone may lead to safer use of nitric oxide and improved clinical outcomes.
出生时,肺血管阻力显著降低,使肺能够建立气体交换。当这种正常的气体交换适应过程未发生时,就会出现新生儿持续性肺动脉高压(PPHN)。我们回顾了用于研究PPHN发病机制和治疗方法的动物模型。文中描述了急性模型,如急性缺氧和血管收缩剂输注,以及在出生前和出生后立即建立的PPHN慢性模型。吸入一氧化氮是一种重要的新兴PPHN治疗方法。我们回顾了一氧化氮受体机制,包括可溶性鸟苷酸环化酶,它在受到一氧化氮刺激时产生环磷酸鸟苷(cGMP),以及磷酸二酯酶,它控制着cGMP信号转导的强度和持续时间。更好地理解这些血管张力调节机制可能会使一氧化氮的使用更安全,并改善临床结果。