Maternal infection regulates BDNF and NGF expression in fetal and neonatal brain and maternal-fetal unit of the rat

J Neuroimmunol. 2003 May;138(1-2):49-55. doi: 10.1016/s0165-5728(03)00095-x.

Abstract

Maternal infection during pregnancy is associated with increased risk for neurodevelopmental disorders. Lipopolysaccharide (LPS) or saline was administered to rats to model maternal infection, and levels of brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) in maternal plasma, placenta, amniotic fluid, fetal liver/spleen, fetal brain, and cerebral cortex after birth were determined by ELISA or semiquantitative Western blot analysis. BDNF expression was significantly increased in the fetal brain (p=0.039); NGF expression was significantly increased in neonatal cortex (p=0.0009). Neurotrophic factor expression was also altered in other tissues of the maternal-fetal unit. Abnormal expression of neurotrophic factors represents a potential mechanism through which maternal infection increases risk for neurodevelopmental disorders.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Newborn
  • Brain / embryology
  • Brain / immunology
  • Brain / metabolism*
  • Brain-Derived Neurotrophic Factor / antagonists & inhibitors
  • Brain-Derived Neurotrophic Factor / biosynthesis*
  • Brain-Derived Neurotrophic Factor / blood
  • Escherichia coli Infections / blood
  • Escherichia coli Infections / immunology
  • Escherichia coli Infections / metabolism*
  • Female
  • Fetus
  • Injections, Intraperitoneal
  • Lipopolysaccharides / toxicity
  • Liver / embryology
  • Liver / immunology
  • Liver / metabolism
  • Male
  • Maternal-Fetal Exchange / immunology*
  • Nerve Growth Factor / biosynthesis*
  • Placenta / immunology
  • Placenta / metabolism
  • Pregnancy
  • Pregnancy Complications, Infectious / blood
  • Pregnancy Complications, Infectious / immunology
  • Pregnancy Complications, Infectious / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Spleen / embryology
  • Spleen / immunology
  • Spleen / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Up-Regulation / immunology

Substances

  • Brain-Derived Neurotrophic Factor
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Nerve Growth Factor