McCartney Jarret, Richards Elaine M, Wood Charles E, Keller-Wood Maureen
Department of Pharmacodynamics, University of Florida, Gainesville, Florida, USA Department of Physiology and Functional Genomics, University of Florida, Gainesville, Florida, USA.
Department of Pharmacodynamics, University of Florida, Gainesville, Florida, USA.
Physiol Rep. 2014 Jul 16;2(7):e12066. doi: 10.14814/phy2.12066.
This study was designed to determine the effects of corticosteroids at MR in the late-gestation fetal lung. Since both the mineralocorticoid receptor (MR) and the glucocorticoid receptor (GR) are expressed at relatively high levels in the fetal lung, endogenous corticosteroids may act at MR as well as GR in the preterm fetal lung. The GR agonist, betamethasone, the MR agonist, aldosterone, or both were infused intravenously for 48 h in ovine fetuses of approximately 130 days gestation. Effects on airway pressures during stepwise inflation of the in situ lung, expression of ENaC alpha (SCNN1A), ENaC beta (SCNN1B), and Na,K ATPase (ATP1A1), and elastin and collagen content were determined after the infusions. We found that aldosterone significantly reduced the airway pressure measured during the initial step in inflation of the lung, although aldosterone had no overall effect on lung compliance, nor did aldosterone induce expression of ENaCα, ENaCβ or Na,K ATPaseα1. Betamethasone significantly increased expression of the epithelial sodium channel (ENaC) subunit mRNAs, and collagen and elastin content in the lungs, although this dose of betamethasone also had no effect on lung compliance. There was no synergy between effects of the MR and GR agonists. Transcriptomic analysis suggested that although aldosterone did not alter genes in pathways related to epithelial sodium transport, aldosterone did alter genes in pathways involved in cell proliferation in the lungs. The results are consistent with corticosteroid-induced fluid reabsorption at birth through GR rather than MR, but suggest that MR facilitates lung maturation, and may contribute to inflation with the first breaths via mechanisms distinct from known aldosterone effects in other epithelia.
本研究旨在确定皮质类固醇在妊娠晚期胎儿肺脏中作用于盐皮质激素受体(MR)的效果。由于盐皮质激素受体(MR)和糖皮质激素受体(GR)在胎儿肺脏中均有较高水平的表达,内源性皮质类固醇可能在早产胎儿肺脏中同时作用于MR和GR。将GR激动剂倍他米松、MR激动剂醛固酮或两者静脉输注给妊娠约130天的绵羊胎儿,持续48小时。输注后,测定原位肺脏逐步充气过程中的气道压力、ENaCα(SCNN1A)、ENaCβ(SCNN1B)和钠钾ATP酶(ATP1A1)的表达以及弹性蛋白和胶原蛋白含量。我们发现,醛固酮显著降低了肺脏充气初始阶段测得的气道压力,尽管醛固酮对肺顺应性没有总体影响,也未诱导ENaCα、ENaCβ或钠钾ATP酶α1的表达。倍他米松显著增加了肺脏中上皮钠通道(ENaC)亚基mRNA以及胶原蛋白和弹性蛋白的含量,尽管该剂量的倍他米松对肺顺应性也没有影响。MR和GR激动剂的作用之间没有协同作用。转录组分析表明,尽管醛固酮未改变与上皮钠转运相关途径中的基因,但醛固酮确实改变了肺脏中参与细胞增殖途径中的基因。这些结果与皮质类固醇通过GR而非MR在出生时诱导液体重吸收一致,但表明MR促进肺成熟,并可能通过与已知醛固酮在其他上皮细胞中的作用不同的机制,有助于首次呼吸时的充气。