Department of Physiology and Pathophysiology, Peking University, Health Science Center, Beijing, China.
Physiol Rev. 2010 Oct;90(4):1291-335. doi: 10.1152/physrev.00032.2009.
During the development of the pulmonary vasculature in the fetus, many structural and functional changes occur to prepare the lung for the transition to air breathing. The development of the pulmonary circulation is genetically controlled by an array of mitogenic factors in a temporo-spatial order. With advancing gestation, pulmonary vessels acquire increased vasoreactivity. The fetal pulmonary vasculature is exposed to a low oxygen tension environment that promotes high intrinsic myogenic tone and high vasocontractility. At birth, a dramatic reduction in pulmonary arterial pressure and resistance occurs with an increase in oxygen tension and blood flow. The striking hemodynamic differences in the pulmonary circulation of the fetus and newborn are regulated by various factors and vasoactive agents. Among them, nitric oxide, endothelin-1, and prostaglandin I(2) are mainly derived from endothelial cells and exert their effects via cGMP, cAMP, and Rho kinase signaling pathways. Alterations in these signaling pathways may lead to vascular remodeling, high vasocontractility, and persistent pulmonary hypertension of the newborn.
在胎儿肺部血管发育过程中,会发生许多结构和功能上的变化,为肺部向空气呼吸过渡做准备。肺循环的发育受遗传控制,受一系列有丝分裂原因子以时空顺序调控。随着胎龄的增加,肺血管的血管反应性增加。胎儿肺部血管暴露于低氧张力环境中,促进了高内在肌源性张力和高血管收缩性。出生时,随着氧分压和血流量的增加,肺动脉压和阻力显著降低。胎儿和新生儿肺部循环的显著血流动力学差异受多种因素和血管活性物质的调节。其中,一氧化氮、内皮素-1 和前列环素 I(2)主要来源于内皮细胞,通过 cGMP、cAMP 和 Rho 激酶信号通路发挥作用。这些信号通路的改变可能导致血管重塑、高血管收缩性和新生儿持续性肺动脉高压。