Phorbol ester contracts rabbit thoracic aorta by increasing intracellular calcium and by activating calcium influx

Biochem Biophys Res Commun. 1986 Aug 14;138(3):1362-9. doi: 10.1016/s0006-291x(86)80433-8.

Abstract

The ability of the phorbol ester tumor promoter, PDB, to activate contraction and stimulate calcium influx was investigated in rabbit thoracic aorta. PDB caused a strong, slowly-developing sustained contraction in physiological salt solution which was concentration-related (0.01 to 10.0 microM). PDB-induced contractions (0.1 microM) in calcium-free medium were attenuated but not prevented. PDB (1.0 microM) maximally stimulated Ca influx above basal control, vehicle = 39.2 +/- 2.2; PDB 1.0 microM = 70.7 +/- 6.7 mumoles Ca/kg tissue; N = 16, p less than 0.01). These data suggest that PDB activates rabbit thoracic aorta by a combination of intracellular and extracellular calcium dependent mechanisms.

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Calcium / physiology*
  • Colforsin / pharmacology
  • Cytoplasm / physiology
  • Extracellular Space / physiology
  • Male
  • Muscle Contraction / drug effects
  • Muscle, Smooth, Vascular / physiology*
  • Nifedipine / pharmacology
  • Phorbol 12,13-Dibutyrate
  • Phorbol Esters / pharmacology*
  • Prazosin / pharmacology
  • Protein Kinase C / physiology
  • Rabbits
  • Time Factors

Substances

  • Phorbol Esters
  • Colforsin
  • Phorbol 12,13-Dibutyrate
  • Protein Kinase C
  • Nifedipine
  • Calcium
  • Prazosin