Prenatal development is linked to bronchial reactivity: epidemiological and animal model evidence

Katharine C Pike1, Shelley A Davis2, Samuel A Collins3

  • 11] Clinical and Experimental Sciences Academic Unit, University of Southampton Faculty of Medicine, Southampton, UK [2] NIHR Southampton Respiratory Biomedical Research Unit [3].

Scientific Reports
|April 18, 2014
PubMed

Insights

Maternal nutrition during pregnancy impacts offspring respiratory health. Poor prenatal nutrition in rats and humans is linked to increased bronchial hyperreactivity, suggesting developmental programming influences lung function.

Area of Science:

  • Developmental biology
  • Respiratory medicine
  • Perinatal nutrition

Background:

  • Chronic cardiorespiratory disease is linked to low birthweight, highlighting the significance of the prenatal environment.
  • While prenatal factors influencing fetal growth are recognized, the specific mechanisms remain unclear.

Purpose of the Study:

  • To investigate the influence of developmental programming on bronchial hyperreactivity using an animal model.
  • To seek evidence for comparable associations between prenatal development and bronchial hyperreactivity in humans.

Main Methods:

  • Pregnant Wistar rats received control or protein-restricted diets; offspring bronchoconstrictor responses and lung morphometrics were analyzed.
  • A human mother-child cohort study correlated ultrasound-measured fetal growth with bronchial hyperreactivity (methacholine challenge) at age six.

Main Results:

  • Offspring of protein-restricted rats exhibited enhanced bronchoconstriction compared to controls, without structural airway alterations.
  • Human children with reduced abdominal circumference growth during early gestation showed greater bronchial hyperreactivity.

Conclusions:

  • Imbalanced maternal nutrition during pregnancy leads to bronchial hyperreactivity in offspring.
  • Prenatal environmental influences, including nutrition, may play a significant role in human respiratory health and disease development.

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