Airway expression of the epithelial sodium channel α-subunit correlates with cortisol in term newborns

Pediatrics. 2011 Aug;128(2):e414-21. doi: 10.1542/peds.2011-0167. Epub 2011 Jul 18.

Abstract

Background: Glucocorticoids have profound effects on lung maturation and function. In in vitro and animal models, they induce epithelial sodium channels (ENaCs) in the airway epithelium, a process that is important to perinatal lung fluid clearance.

Objective: The objective of this study was to determine whether, in newborn infants, airway ENaC expression is associated with cortisol concentrations.

Methods: Cord blood, saliva, and cells from nasal epithelium were obtained from 69 infants delivered at term. Epithelial and saliva sampling was repeated 3 times: <3, 22 to 29, and 40 to 54 hours postnatally. Cortisol, thyrotropin, and free triiodothyronine concentrations were measured with immunoassays, and expression of α-ENaC and β-ENaC was quantified with real-time reverse-transcriptase polymerase chain reaction.

Results: Expression of α-ENaC <30 minutes postnatally correlated with cord plasma cortisol in infants delivered by elective cesarean delivery. In addition, in the total study population <2 hours postnatally, α-ENaC expression correlated with salivary cortisol concentrations. β-ENaC expression, in contrast, showed no association with cortisol concentrations. A significant decrease in β-ENaC expression during the first postnatal day was revealed, whereas timing of the peak in α-ENaC expression seemed to depend on mode of delivery.

Conclusions: These results support a role in humans for endogenous glucocorticoids in the regulation of airway ion transport. This finding may be a physiologic mechanism mediating pulmonary adaptation in the newborn infant.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • Epithelial Sodium Channels / biosynthesis*
  • Female
  • Fetal Blood / metabolism
  • Gene Expression Regulation, Developmental*
  • Humans
  • Hydrocortisone / blood*
  • Hydrocortisone / metabolism
  • Infant, Newborn
  • Male
  • Nasal Mucosa / metabolism*
  • Pregnancy
  • Saliva / metabolism

Substances

  • Biomarkers
  • Epithelial Sodium Channels
  • SCNN1A protein, human
  • Hydrocortisone