Gualdoni Gisela Soledad, Jacobo Patricia Verónica, Barril Camila, Ventureira Martín Ricardo, Cebral Elisa
Laboratorio de Reproducción y Fisiología Materno-Embrionaria, Instituto de Biodiversidad y Biología Experimental y Aplicada (IBBEA), Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET), Departamento de Biodiversidad y Biología Experimental (DBBE), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
Front Physiol. 2022 Feb 2;12:815760. doi: 10.3389/fphys.2021.815760. eCollection 2021.
Adequate placentation, placental tissue remodeling and vascularization is essential for the success of gestation and optimal fetal growth. Recently, it was suggested that abnormal placenta induced by maternal alcohol consumption may participate in fetal growth restriction and relevant clinical manifestations of the Fetal Alcohol Spectrum Disorders (FASD). Particularly, periconceptional alcohol consumption up to early gestation can alter placentation and angiogenesis that persists in pregnancy beyond the exposure period. Experimental evidence suggests that abnormal placenta following maternal alcohol intake is associated with insufficient vascularization and defective trophoblast development, growth and function in early gestation. Accumulated data indicate that impaired vascular endothelial growth factor (VEGF) system, including their downstream effectors, the nitric oxide (NO) and metalloproteinases (MMPs), is a pivotal spatio-temporal altered mechanism underlying the early placental vascular alterations induced by maternal alcohol consumption. In this review we propose that the periconceptional alcohol intake up to early organogenesis (first trimester) alters the VEGF-NO-MMPs system in trophoblastic-decidual tissues, generating imbalances in the trophoblastic proliferation/apoptosis, insufficient trophoblastic development, differentiation and migration, deficient labyrinthine vascularization, and uncompleted remodelation and transformation of decidual spiral arterioles. Consequently, abnormal placenta with insufficiency blood perfusion, vasoconstriction and reduced labyrinthine blood exchange can be generated. Herein, we review emerging knowledge of abnormal placenta linked to pregnancy complications and FASD produced by gestational alcohol ingestion and provide evidence of the early abnormal placental angiogenesis-vascularization and growth associated to decidual-trophoblastic dysregulation of VEGF system after periconceptional alcohol consumption up to mid-gestation, in a mouse model.
充足的胎盘形成、胎盘组织重塑和血管生成对于妊娠成功及胎儿最佳生长至关重要。最近有研究表明,母亲饮酒所致的胎盘异常可能参与胎儿生长受限及胎儿酒精谱系障碍(FASD)的相关临床表现。特别是,从受孕前到妊娠早期饮酒可改变胎盘形成和血管生成,这种改变在暴露期过后的孕期仍持续存在。实验证据表明,母亲饮酒后胎盘异常与血管生成不足以及妊娠早期滋养层细胞发育、生长和功能缺陷有关。积累的数据表明,血管内皮生长因子(VEGF)系统受损,包括其下游效应分子一氧化氮(NO)和金属蛋白酶(MMPs),是母亲饮酒所致早期胎盘血管改变的关键时空改变机制。在本综述中,我们提出,受孕前至器官形成早期(孕早期)饮酒会改变滋养层-蜕膜组织中的VEGF-NO-MMPs系统,导致滋养层细胞增殖/凋亡失衡、滋养层细胞发育、分化和迁移不足、迷路血管生成不足以及蜕膜螺旋小动脉重塑和转化不完全。因此,可产生血液灌注不足、血管收缩和迷路血液交换减少的异常胎盘。在此,我们综述了与妊娠并发症和孕期饮酒所致FASD相关的异常胎盘的新认识,并在小鼠模型中提供了受孕前至妊娠中期饮酒后与蜕膜-滋养层VEGF系统失调相关的早期胎盘异常血管生成-血管化和生长的证据。