Lorquet S, Pequeux C, Munaut C, Foidart J M
Department Universitaire de Gynécologie Obstétrique, Hôpital de La Citadelle, Liège, Belgique.
Acta Clin Belg. 2010 Jul-Aug;65(4):237-41. doi: 10.1179/acb.2010.051.
Preeclampsia, a pregnancy-specific syndrome characterized by hypertension, proteinuria and oedema, resolves on placental delivery. Its pathogenesis is thought to be associated to a hypoxic placenta. Placental hypoxia is responsible for the maternal vascular dysfunction via the increased placental release of anti-angiogenic factors such as soluble flt1 and endoglin. These soluble receptors bind VEGF, PLGF and TGFbeta1 and 3 in the maternal circulation, causing endothelial dysfunction in many maternal tissues. Despite these recent and important new molecular findings, it is important to consider that normal pregnancy is also characterized by systemic inflammation, oxidative stress and alterations in levels of angiogenic factors and vascular reactivity. Both the placenta and maternal vasculatures are major sources of reactive oxygen and nitrogen species which can produce powerful pro-oxidants that covalently modify proteins and alter vascular function in preeclampsia. Finally, the recent demonstration of activating auto-antibodies to the Angiotensin 1 receptor that experimentally play a major pathogenic role in preeclampsia further indicates the pleiotropism of aetiologies of this condition.
子痫前期是一种特定于妊娠的综合征,其特征为高血压、蛋白尿和水肿,在胎盘娩出后症状会消失。其发病机制被认为与胎盘缺氧有关。胎盘缺氧通过增加抗血管生成因子(如可溶性flt1和内皮糖蛋白)的胎盘释放,导致母体血管功能障碍。这些可溶性受体在母体循环中与VEGF、PLGF和TGFbeta1及3结合,导致许多母体组织中的内皮功能障碍。尽管有这些最新且重要的分子学新发现,但必须考虑到正常妊娠也具有全身炎症、氧化应激以及血管生成因子水平和血管反应性改变的特征。胎盘和母体血管都是活性氧和氮物质的主要来源,这些物质可产生强大的促氧化剂,共价修饰蛋白质并改变子痫前期的血管功能。最后,最近发现的针对血管紧张素1受体的激活自身抗体在子痫前期实验中起主要致病作用,这进一步表明了该病症病因的多效性。