Netsanet Adom, Seedorf Gregory J, Abman Steven H, Taglauer Elizabeth S
Department of Pediatrics, Pediatric Heart Lung Center, University of Colorado School of Medicine, Aurora, Colorado, United States.
Department of Pediatrics, Boston Medical Center, Boston University Chobanian and Avedisian School of Medicine, Boston, Massachusetts, United States.
Am J Physiol Lung Cell Mol Physiol. 2025 Jan 1;328(1):L197-L205. doi: 10.1152/ajplung.00204.2024. Epub 2024 Dec 19.
Intrauterine inflammation from chorioamnionitis (CA) is associated with placental dysfunction and increased risk of bronchopulmonary dysplasia (BPD), the chronic lung disease of prematurity. Antenatal steroid (ANS) treatment improves early respiratory outcomes for premature infants. However, it remains unclear whether ANS improves long-term respiratory outcomes, and whether these effects are mediated through the improvement of placental dysfunction and/or direct impact on the fetal lung. We hypothesized that maternal ANS therapy preserves long-term lung development and impacts placental structural changes and gene expression in experimental CA with features of BPD. Pregnant rat dams were administered either saline (CTL), intra-amniotic (IA) endotoxin (ETX), ETX plus intramuscular (IM) betamethasone (ETX + BETA), or IM BM alone (BETA) on (E20). We collected placental tissue at delivery (E22) and infant lung tissue on the (DOL) . In comparison with controls, IA ETX had impaired infant lung growth and function. Maternal BM treatment of ETX-exposed pregnant dams reduced infant total lung resistance by 15.3% ( < 0.05), improved infant lung compliance by 9.5% ( < 0.05), preserved alveolar and vascular growth ( < 0.05), and improved right ventricular hypertrophy (RVH) by 42.4% ( < 0.05). ETX + BETA pregnancies were also associated with normalization of placental spiral artery modification and altered placental gene expression. These included the upregulation of placental prolactin, which has regulatory effects on pregnancy homeostasis and has been clinically associated with decreased BPD risk. The current study identifies parallel lung and placental changes associated with ANS treatment, providing a foundation for future studies to identify alternate antenatal therapies with more specific efficacy for BPD prevention. We performed parallel neonatal lung and placental analyses in a preclinical model to characterize the impact of antenatal betamethasone in experimental chorioamnionitis. Antenatal steroids improved long-term respiratory outcomes and were associated with concurrent structural and molecular changes in the placenta. This study establishes an important model system for future analyses to evaluate mechanistic links determining whether the long-term impact of antenatal steroids on lung development may be through alteration of placental function.
绒毛膜羊膜炎(CA)引起的宫内炎症与胎盘功能障碍以及支气管肺发育不良(BPD,即早产儿慢性肺部疾病)风险增加相关。产前类固醇(ANS)治疗可改善早产儿的早期呼吸结局。然而,目前尚不清楚ANS是否能改善长期呼吸结局,以及这些作用是否通过改善胎盘功能障碍和/或对胎儿肺的直接影响来介导。我们假设母体ANS治疗可保护长期肺发育,并影响具有BPD特征的实验性CA中的胎盘结构变化和基因表达。在妊娠第20天(E20),给怀孕的大鼠母鼠分别注射生理盐水(CTL)、羊膜内(IA)注射内毒素(ETX)、ETX加肌肉注射(IM)倍他米松(ETX + BETA)或单独肌肉注射倍他米松(BETA)。在分娩时(E22)收集胎盘组织,并在出生后第14天(DOL 14)收集幼鼠肺组织。与对照组相比,IA ETX导致幼鼠肺生长和功能受损。对暴露于ETX的怀孕母鼠进行母体倍他米松治疗可使幼鼠总肺阻力降低15.3%(P < 0.05),幼鼠肺顺应性提高9.5%(P < 0.05),保留肺泡和血管生长(P < 0.05),并使右心室肥厚(RVH)改善42.4%(P < 0.05)。ETX + BETA妊娠还与胎盘螺旋动脉重塑正常化和胎盘基因表达改变有关。这些变化包括胎盘催乳素上调,其对妊娠稳态具有调节作用,并且在临床上与BPD风险降低相关。本研究确定了与ANS治疗相关的肺和胎盘的平行变化,为未来研究确定对预防BPD具有更特异性疗效的替代产前治疗方法奠定了基础。我们在一个临床前模型中对新生儿肺和胎盘进行了平行分析,以表征产前倍他米松在实验性绒毛膜羊膜炎中的影响。产前类固醇改善了长期呼吸结局,并与胎盘的结构和分子变化同时出现。本研究建立了一个重要的模型系统,用于未来的分析,以评估确定产前类固醇对肺发育的长期影响是否可能通过改变胎盘功能的机制联系。