Maternal and fetal circulating sKL and ET-1 levels as function of normal labor at term

J Matern Fetal Neonatal Med. 2011 Feb;24(2):324-9. doi: 10.3109/14767058.2010.496502. Epub 2010 Jul 7.

Abstract

Objectives: To determine whether labor is associated with alterations of the levels of soluble c-kit ligand (sKL) and endothelin-1 (ET-1) in maternal plasma and umbilical cord blood.

Methods: The sKL and ET-1 levels were investigated in umbilical cord and maternal plasma on the day of delivery in 18 pregnant women with vaginal delivery during labor, 18 non-pregnant women and 9 pregnant women before cesarean delivery, using an ELISA assay.

Results: Umbilical cord plasma sKL levels were significantly higher than the maternal plasma in both types of delivery (p = 0.0001, p < 0.0001, respectively). However, maternal plasma ET-1 levels in the presence of labor were significantly higher than the cesarean delivery group (p < 0.0001). No difference was noted for sKL and ET-1 in umbilical cord vessels of both groups. Furthermore, a highly significant inverse correlation was documented between the individual levels of cord plasma ET-1 and the levels of cord plasma sKL (r = -0.6269, p = 0.0054).

Conclusions: The sKL levels found in umbilical cord plasma are consistent with the pleiotropic effects of sKL in facilitating the transition of the fetus to the neonatal stage. The reduced ET-1 maternal plasma levels, compared to non-pregnant women, probably are indicative of a putative mechanism for embryo protection from vasoconstriction sequelae. This assumption is strengthened by the corresponding ET-1 levels in umbilical cord plasma.

MeSH terms

  • Adult
  • Case-Control Studies
  • Endothelin-1 / analysis
  • Endothelin-1 / blood*
  • Endothelin-1 / metabolism
  • Female
  • Fetal Blood / chemistry
  • Fetal Blood / metabolism*
  • Fetus / metabolism
  • Health
  • Humans
  • Labor, Obstetric / blood*
  • Labor, Obstetric / metabolism
  • Mothers*
  • Placental Circulation / physiology
  • Pregnancy
  • Solubility
  • Stem Cell Factor / analysis
  • Stem Cell Factor / blood*
  • Stem Cell Factor / metabolism
  • Term Birth / blood*
  • Term Birth / metabolism
  • Young Adult

Substances

  • Endothelin-1
  • Stem Cell Factor