SK&F 96365 inhibits intracellular Ca2+ pumps and raises cytosolic Ca2+ concentration without production of nitric oxide and von Willebrand factor

Cell Calcium. 1996 Dec;20(6):501-8. doi: 10.1016/s0143-4160(96)90092-5.

Abstract

The effects of the imidazole compound SK&F 96365 on Ca2+ movements and production of nitric oxide (NO) and von Willebrand factor (vWF) have been investigated in human endothelial cells. Changes in cytosolic Ca2+ concentration ([Ca2+]i) were measured with Fura-2. Real-time production of NO was monitored with a porphyrinic microsensor and the release of vWF with an enzyme-linked immunosorbent assay. Irrespective of the transmembrane Ca2+ gradient, 30 microM SK&F 96365 doubled [Ca2+]i suggesting a Ca2+ release from intracellular stores. The SK&F 96365-induced [Ca2+]i rise was not accompanied by detectable NO and vWF production, while 1 microM thapsigargin enhanced [Ca2+]i 2.5 times, doubled the secretion of vWF and increased the NO production to 10 +/- 4 nM (n = 5). Pretreatment with SK&F 96365 prevented thapsigargin from increasing [Ca2+]i, NO production and vWF secretion. To investigate the mechanism by which SK&F 96365 released Ca2+ from internal pools, its effect and that of thapsigargin on the ATP-dependent 45Ca2+ uptake into platelet membrane vesicles were compared. SK&F 96365 as thapsigargin, dose-dependently reduced the initial rate of 45Ca2+ uptake. In conclusion, we demonstrate that, in the absence of Ca2+ entry from the extracellular space, the [Ca2+]i increase elicited by SK&F 96365 or thapsigargin is not sufficient to initiate NO synthesis and vWF secretion. This confirms the important role of Ca2+ influx in endothelial secretion processes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Biological Transport / drug effects
  • Biological Transport / physiology
  • Blood Platelets / enzymology
  • Blood Platelets / ultrastructure
  • Calcium / metabolism*
  • Calcium / pharmacokinetics
  • Calcium Channel Blockers / pharmacology*
  • Calcium Radioisotopes / pharmacokinetics
  • Calcium-Transporting ATPases / antagonists & inhibitors*
  • Calcium-Transporting ATPases / metabolism
  • Cells, Cultured / drug effects
  • Cells, Cultured / enzymology
  • Cells, Cultured / metabolism
  • Cytoplasm / metabolism
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Epithelial Cells
  • Epithelium / drug effects
  • Epithelium / enzymology
  • Humans
  • Imidazoles / pharmacology*
  • Intracellular Membranes / metabolism
  • Nitric Oxide / biosynthesis*
  • Thapsigargin / pharmacology
  • Umbilical Veins / cytology
  • von Willebrand Factor / biosynthesis*
  • von Willebrand Factor / metabolism

Substances

  • Calcium Channel Blockers
  • Calcium Radioisotopes
  • Enzyme Inhibitors
  • Imidazoles
  • von Willebrand Factor
  • Nitric Oxide
  • Thapsigargin
  • Adenosine Triphosphate
  • Calcium-Transporting ATPases
  • 1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1H-imidazole
  • Calcium