Characterization of thromboxane A2 receptors in the human fetal placental vessels and umbilical vein

Clin Exp Pharmacol Physiol. 1986 Jan;13(1):83-6. doi: 10.1111/j.1440-1681.1986.tb00319.x.

Abstract

An in vitro examination has been made of the thromboxane A2 receptors in human fetal placental villous vessels and umbilical veins utilizing the TxA2 agonist U46619 and its competitive antagonist AH22921. U46619 was a potent constrictor of both preparations. The EC50 were 25.3 nmol/l (s.e.m. = 2.5, n = 8) for causing constriction of perfused villous vessels and 22 nmol/l (s.e.m. = 5, n = 17) for contraction of the venous longitudinal strip. AH22921 competitively antagonized responses to U46619 in both preparations. The pA2 values were not significantly different and their 95% confidence limits, obtained for its ability to antagonize responses to U46619 in villous vessels and the umbilical vein, were 8.0 (7.3-8.8) and 7.1 (6.3-7.9) respectively. It is concluded that TxA2 receptors in both the human fetal placental villous vessels and umbilical vein may be similar. They also may be similar to those in human platelets and pulmonary blood vessels.

MeSH terms

  • Biphenyl Compounds / pharmacology
  • Chorionic Villi / analysis
  • Female
  • Humans
  • Placenta / blood supply*
  • Pregnancy
  • Prostaglandin Endoperoxides, Synthetic / metabolism
  • Receptors, Cell Surface / metabolism*
  • Receptors, Prostaglandin / metabolism*
  • Receptors, Thromboxane
  • Umbilical Veins / metabolism*

Substances

  • Biphenyl Compounds
  • Prostaglandin Endoperoxides, Synthetic
  • Receptors, Cell Surface
  • Receptors, Prostaglandin
  • Receptors, Thromboxane
  • AH 22921