Maternal protein restriction during perinatal life affects lung mechanics and the surfactant system during early

Reza Khazaee1,2, Lynda A McCaig3, Cory Yamashita1,3,4

  • 1Department of Physiology & Pharmacology, The University of Western Ontario, London, Ontario, Canada.

Plos One
|April 20, 2019
PubMed

Insights

Fetal growth retardation (FGR) impacts female neonates' lung function and surfactant levels differently than males. Female offspring showed reduced lung compliance and altered surfactant, unlike males, indicating sex-specific pulmonary effects.

Area of Science:

  • Neonatal physiology
  • Pulmonary development
  • Reproductive biology

Background:

  • Fetal growth retardation (FGR) is a condition with limited understanding of its sex-specific effects on neonatal lungs.
  • Investigating FGR's impact on lung mechanics and the surfactant system is crucial for neonatal health outcomes.

Purpose of the Study:

  • To test the hypothesis that FGR alters lung mechanics and the surfactant system in a sex-specific manner during the neonatal period.
  • To analyze the effects of a maternal low protein diet during gestation and lactation on offspring pulmonary function.

Main Methods:

  • A rat model of FGR was established using a low protein diet in dams.
  • Lung mechanics were assessed using a FlexiVent ventilator in male and female pups at postnatal days 7 and 21.
  • Surfactant pool size, subfractions, and surface tension-reducing ability were analyzed from lung lavage samples.

Main Results:

  • Female FGR offspring exhibited significantly lower lung compliance and higher tissue elastance at postnatal day 21 compared to controls.
  • Female offspring from the low protein diet showed reduced surfactant pool sizes at postnatal day 1.
  • These pulmonary and surfactant alterations were not observed in male offspring.

Conclusions:

  • Fetal growth retardation has a differential impact on pulmonary function and surfactant composition in female versus male neonates.
  • The findings highlight sex-specific vulnerabilities in lung development following FGR.
  • Further research is warranted to understand the long-term implications of these sex-based differences.

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