Holme Ane M, Holm Maia B, Roland Marie C P, Horne Hildegunn, Michelsen Trond M, Haugen Guttorm, Henriksen Tore
Department of Obstetrics, Oslo University Hospital; Institute of Clinical Medicine, University of Oslo;
Department of Obstetrics, Oslo University Hospital; Institute of Clinical Medicine, University of Oslo.
J Vis Exp. 2017 Aug 2(126):55847. doi: 10.3791/55847.
The human placenta is highly inaccessible for research while still in utero. The current understanding of human placental physiology in vivo is therefore largely based on animal studies, despite the high diversity among species in placental anatomy, hemodynamics and duration of the pregnancy. The vast majority of human placenta studies are ex vivo perfusion studies or in vitro trophoblast studies. Although in vitro studies and animal models are essential, extrapolation of the results from such studies to the human placenta in vivo is uncertain. We aimed to study human placenta physiology in vivo at term, and present a detailed protocol of the method. Exploiting the intraabdominal access to the uterine vein just before the uterine incision during planned cesarean section, we collect blood samples from the incoming and outgoing vessels on the maternal and fetal sides of the placenta. When combining concentration measurements from blood samples with volume blood flow measurements, we are able to quantify placental and fetal uptake and release of any compound. Furthermore, placental tissue samples from the same mother-fetus pairs can provide measurements of transporter density and activity and other aspects of placental functions in vivo. Through this integrative use of the 4-vessel sampling method we are able to test some of the current concepts of placental nutrient transfer and metabolism in vivo, both in normal and pathological pregnancies. Furthermore, this method enables the identification of substances secreted by the placenta to the maternal circulation, which could be an important contribution to the search for biomarkers of placenta dysfunction.
人类胎盘在子宫内时极难用于研究。因此,目前对人类胎盘体内生理学的理解很大程度上基于动物研究,尽管胎盘解剖结构、血流动力学和孕期时长在物种间存在高度差异。绝大多数人类胎盘研究是体外灌注研究或体外滋养层细胞研究。虽然体外研究和动物模型至关重要,但将此类研究结果外推至人类胎盘体内情况仍不确定。我们旨在研究足月时人类胎盘的体内生理学,并给出该方法的详细方案。利用计划性剖宫产术中子宫切开前经腹进入子宫静脉的途径,我们从胎盘母胎侧的流入和流出血管采集血样。将血样浓度测量与血流量测量相结合时,我们能够量化胎盘和胎儿对任何化合物的摄取和释放。此外,来自同一母婴对的胎盘组织样本可提供转运体密度和活性以及胎盘体内功能其他方面的测量数据。通过综合运用四血管采样方法,我们能够在正常和病理妊娠中检验当前一些关于胎盘营养物质转运和代谢的体内概念。此外,该方法能够识别胎盘分泌至母体循环中的物质,这可能对寻找胎盘功能障碍的生物标志物有重要贡献。