Modulation of [3H]muscimol binding in rat cerebellar and cerebral cortical membranes by picrotoxin, pentobarbitone, and etomidate

J Neurochem. 1983 Aug;41(2):418-25. doi: 10.1111/j.1471-4159.1983.tb04758.x.


Modulation of [3H]muscimol binding by picrotoxin, pentobarbitone, and etomidate was investigated in rat cerebellar and cerebral cortical membranes. In cerebellum, at 37 degrees C in the presence of chloride ions (150 mM), picrotoxin and picrotoxinin decreased specific [3H]muscimol binding to 43 +/- 3% of control, with an EC50 of 1.2 +/- 0.1 microM. [3H]Muscimol saturation experiments in the presence and absence of picrotoxin indicated that the picrotoxin effect was primarily due to a loss of high-affinity muscimol sites with KD approximately equal to 10 nM. Pentobarbitone enhanced specific [3H]muscimol binding to 259 +/- 3% of control, with EC50 = 292 +/- 37 microM, and etomidate increased binding to 298 +/- 18%, with EC50 = 7.1 +/- 1.0 microM. The influence of temperature and chloride ion concentration on these effects was investigated by comparing experiments at 37 and 0 degrees C in the presence or absence of chloride at constant ionic strength. The results indicate that studies at 0 degrees C underestimate the coupling between GABA receptors and barbiturate sites and that they greatly overestimate the importance of chloride ions in this phenomenon. In cerebral cortical membranes (37 degrees C, 150 mM Cl-), the effect of picrotoxin was similar to that observed in cerebellum, whereas the effects of pentobarbitone and etomidate were greater, but occurred at higher concentrations.

MeSH terms

  • Animals
  • Cell Membrane / metabolism
  • Cerebellar Cortex / metabolism*
  • Cerebral Cortex / metabolism*
  • Etomidate / pharmacology*
  • Imidazoles / pharmacology*
  • Kinetics
  • Male
  • Muscimol / metabolism*
  • Organ Specificity
  • Oxazoles / metabolism*
  • Pentobarbital / pharmacology*
  • Picrotoxin / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Cell Surface / drug effects
  • Receptors, Cell Surface / metabolism*
  • Receptors, GABA-A


  • Imidazoles
  • Oxazoles
  • Receptors, Cell Surface
  • Receptors, GABA-A
  • Picrotoxin
  • Muscimol
  • Pentobarbital
  • Etomidate