Washing out of lipophilic compounds induces a transient increase in the passive Ca(2+) leak in permeabilized A7r5 cells

Cell Calcium. 2002 May;31(5):229-33. doi: 10.1016/S0143-4160(02)00051-9.

Abstract

We have investigated how the immunosuppressant drug FK506 affected the basal Ca(2+) leak in permeabilized A7r5 cells. Non-mitochondrial Ca(2+) stores loaded to steady state with Ca(2+) slowly lost their accumulated Ca(2+) during incubation in a Ca(2+)-free efflux medium. FK506 up to 100 microM had no effect on the basal Ca(2+) leak. In contrast, the rate of Ca(2+) release proceeded much faster immediately after washing out FK506. The increase in rate of Ca(2+) release after washing out of this compound depended on both its initial concentration and on the time of pre-incubation. A similar effect was also observed after removing another immunosuppressant drug (rapamycin) and after removing the inositol 1,4,5-trisphosphate receptor inhibitor xestospongin C. Since all these substances have a high octanol/H(2)O partition coefficient and accumulate in the endoplasmic reticulum membrane, we suggest that the transient increase in the basal Ca(2+) leak is due to the sudden removal of these lipophilic substances from the membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta
  • Calcium / metabolism*
  • Cell Membrane Permeability / drug effects*
  • Cell Membrane Permeability / physiology
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Endoplasmic Reticulum / drug effects*
  • Endoplasmic Reticulum / metabolism
  • Immunosuppressive Agents / pharmacology*
  • Intracellular Membranes / drug effects*
  • Intracellular Membranes / metabolism
  • Macrocyclic Compounds
  • Membrane Lipids / metabolism*
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism
  • Oxazoles / pharmacology
  • Rats
  • Sirolimus / pharmacology
  • Tacrolimus / pharmacology*
  • Up-Regulation / drug effects
  • Up-Regulation / physiology

Substances

  • Immunosuppressive Agents
  • Macrocyclic Compounds
  • Membrane Lipids
  • Oxazoles
  • xestospongin A
  • Calcium
  • Sirolimus
  • Tacrolimus