Maternal N-acetylcysteine suppresses fetal inflammatory cytokine responses to maternal lipopolysaccharide

Am J Obstet Gynecol. 2006 Oct;195(4):1053-7. doi: 10.1016/j.ajog.2006.06.081.

Abstract

Objective: Evidence suggests that maternal infections may induce fetal inflammatory responses. Because cytokine actions may be mediated by oxidative stress, we determined whether N-acetylcysteine, an antioxidant, can blunt fetal inflammatory responses to maternal lipopolysaccharide.

Study design: Sprague Dawley near-term rats (n = 16) received intraperitoneal lipopolysaccharide (100 microg/kg) at 30 minutes and saline solution or N-acetylcysteine (300 mg/kg) at 150 minutes. An additional group received N-acetylcysteine before and after lipopolysaccharide administration. At 6 hours, rats were killed, and fetal and maternal blood cytokines were determined.

Results: After maternal lipopolysaccharide administration, fetal blood interleukin-6 markedly increased (3 +/- 2 to 1265 +/- 574 pg/mL); N-acetylcysteine that was given before or before and after lipopolysaccharide administration reduced fetal interleukin-6 response to control levels. A similar trend was observed for interleukin-1beta. No effect of N-acetylcysteine on fetal interleukin-10 levels was observed.

Conclusion: Maternal N-acetylcysteine inhibits fetal cytokine responses to maternal lipopolysaccharide, even when given 2 hours after lipopolysaccharide injection. These results suggest that N-acetylcysteine may protect the fetus from sequelae of maternal inflammation.

MeSH terms

  • Acetylcysteine / pharmacology*
  • Animals
  • Cytokines / biosynthesis*
  • Female
  • Fetal Diseases / prevention & control*
  • Inflammation / prevention & control*
  • Interleukin-1 / blood
  • Interleukin-10 / blood
  • Interleukin-6 / blood
  • Lipopolysaccharides / toxicity*
  • NF-kappa B / physiology
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Cytokines
  • Interleukin-1
  • Interleukin-6
  • Lipopolysaccharides
  • NF-kappa B
  • Interleukin-10
  • Acetylcysteine