Changes of prostacyclin and thromboxane synthesis in the course of mouse liver perfusion. Stimulated thromboxane A2 synthesis of freshly prepared isolated mouse hepatocytes

Prostaglandins Leukot Essent Fatty Acids. 1989 May;36(2):107-12. doi: 10.1016/0952-3278(89)90027-6.

Abstract

The formation of prostacyclin and thromboxane A2 (measured as 6-keto PGF1 alpha and TXB2 by radioimmunoassay) was investigated during a 30 min perfusion of mouse liver in a recirculation system. After cannulation of the portal vein an immediate increase of de novo synthesis and secretion of PGI2 occurred followed by a sharp decrease. Increased PGI2 synthesis was also followed by a continuous increase of TXA2 synthesis and secretion reaching a maximum at the end of the 30 min perfusion. Elevated TXA2 synthesis was also shown in freshly isolated hepatocytes investigated in the course of a 20 min incubation period immediately after the perfusion. However, the elevated TXA2 formation was not observed when it was measured after a 120 min preincubation of the cells. Both PGI2 and TXA2 production could be provoked to a similar extent by the addition of arachidonate and A 23187 immediately after the perfusion or after a 120 min preincubation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / biosynthesis
  • Animals
  • Arachidonic Acid
  • Arachidonic Acids / pharmacology
  • Calcimycin / pharmacology
  • Epoprostenol / biosynthesis*
  • Indomethacin / pharmacology
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism*
  • Mice
  • Perfusion
  • Radioimmunoassay
  • Thromboxane A2 / biosynthesis*
  • Thromboxane B2 / biosynthesis

Substances

  • Arachidonic Acids
  • Arachidonic Acid
  • Calcimycin
  • Thromboxane B2
  • Thromboxane A2
  • 6-Ketoprostaglandin F1 alpha
  • Epoprostenol
  • Indomethacin