High affinity ryanodine binding sites in rat liver endoplasmic reticulum

FEBS Lett. 1990 Apr 24;263(2):317-20. doi: 10.1016/0014-5793(90)81403-b.

Abstract

The binding of [3H]ryanodine to liver microsomal subfractions was investigated. The smooth microsomal membranes were enriched with ryanodine binding sites and also with a polypeptide of 360 kDa. Caffeine completely inhibited [3H]ryanodine binding. Ryanodine also affected the membrane Ca2+ permeability. At low concentrations (less than 10 microM) ryanodine stimulated Ca2+ efflux and at higher concentrations (greater than 50 microM) it blocked Ca2+ efflux. These results suggest that hepatic microsomes contain ryanodine binding sites which can modify the membrane permeability for Ca2+.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alkaloids / metabolism*
  • Animals
  • Caffeine / pharmacology
  • Calcium / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Endoplasmic Reticulum / metabolism*
  • Male
  • Microsomes, Liver / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Cholinergic / drug effects
  • Receptors, Cholinergic / metabolism*
  • Ryanodine / metabolism*
  • Ryanodine Receptor Calcium Release Channel

Substances

  • Alkaloids
  • Receptors, Cholinergic
  • Ryanodine Receptor Calcium Release Channel
  • Ryanodine
  • Caffeine
  • Calcium