Department of Cellular Biology, University of Calabria, Arcavacata di Rende (CS), Italy.
Basic Clin Pharmacol Toxicol. 2012 Jan;110(1):12-8. doi: 10.1111/j.1742-7843.2011.00793.x. Epub 2011 Oct 21.
Sufficient uteroplacental blood flow is essential for normal pregnancy outcome and is accomplished by the coordinated growth and remodelling of the entire maternal uterine vasculature. The main focus of this MiniReview is to provide information on upstream (pre-placental) maternal uterine vascular remodelling that facilitates gestational increases in uterine blood flow. Consideration of the three-dimensional pattern of remodelling (circumferential enlargement versus axial elongation), changes in vessel biomechanical properties, and underlying mechanisms [shear stress, nitric oxide, vascular endothelial growth factor (VEGF)/placental growth factor (PlGF), the renin-angiotensin system] and pathways (local versus systemic; venoarterial exchange) are provided using the rat as the principal animal model, although findings from other species are incorporated wherever possible to provide a comparative perspective. The process of maternal gestational uterine vascular remodelling involves a number of cellular processes and mechanisms, including trophoblast invasion, hyperplasia and hypertrophy, and changes in extracellular matrix composition. In addition, changes in cellular function, e.g. the secretory and contractile properties of smooth muscle and an up-regulation of endothelial vasodilatory influences may contribute to uteroplacental blood flow increases through changes in tone as well as in structure. Future studies aimed at better understanding the inter-relationship between changes in vessel structure (remodelling) and function (reactivity) would likely generate new mechanistic insights into the fascinating process of maternal gestational uterine vascular adaptation and provide a more physiological perspective of the underlying cellular processes involved in its regulation.
足够的胎盘血流对于正常的妊娠结局至关重要,这是通过整个母体子宫血管系统的协调生长和重塑来实现的。本 MiniReview 的主要重点是提供关于前置(胎盘前)母体子宫血管重塑的信息,这有助于妊娠期间子宫血流量的增加。考虑到重塑的三维模式(周向扩大与轴向伸长)、血管生物力学特性的变化以及潜在机制[切应力、一氧化氮、血管内皮生长因子(VEGF)/胎盘生长因子(PlGF)、肾素-血管紧张素系统]和途径(局部与全身;静脉动脉交换),主要使用大鼠作为动物模型提供信息,尽管尽可能纳入了其他物种的发现,以提供比较视角。母体妊娠子宫血管重塑的过程涉及许多细胞过程和机制,包括滋养细胞浸润、增生和肥大,以及细胞外基质组成的变化。此外,细胞功能的变化,例如平滑肌的分泌和收缩特性以及内皮血管舒张影响的上调,可能通过改变张力以及结构来促进胎盘血流增加。未来旨在更好地理解血管结构(重塑)和功能(反应性)变化之间相互关系的研究,可能会为母体妊娠子宫血管适应的迷人过程提供新的机制见解,并为其调节所涉及的潜在细胞过程提供更生理的视角。