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Differential seizure sensitivities to picrotoxinin in two inbred strains of mice (DBA/2J and BALB/c ByJ): parallel changes in GABA receptor-mediated chloride flux and receptor binding.

Abstract
Two strains of mice were shown to possess a differential sensitivity to picrotoxinin-induced convulsions; picrotoxinin elicited both tonic and clonic seizures at lower doses in the DBA/2J (DBA) strain compared to the BALB/c ByJ (BALB) strain. Less protection of picrotoxinin-induced tonic seizures was afforded by pentobarbital in the DBA strain. Biochemical studies revealed that picrotoxin inhibited 36Cl- efflux from forebrain synaptoneurosomes only in the DBA strain. In addition, picrotoxin inhibited pentobarbital-induced 36Cl- efflux to a greater extent in the DBA strain. No differences were observed in the binding of [3H]muscimol or [35S]t-butylbicyclophosphorothionate (TBPS) to forebrain homogenates, while pentobarbital was a less potent inhibitor of [35S]TBPS binding in the DBA strain. These findings suggest a genetic basis for the behavioral differences in convulsant sensitivity as well as for the neurochemical differences in allosteric coupling between convulsant and depressant/anticonvulsant sites associated with the GABA receptor-gated Cl- channel.
AuthorsR D Schwartz, T W Seale, P Skolnick, S M Paul
JournalBrain research (Brain Res) Vol. 481 Issue 1 Pg. 169-74 (Feb 27 1989) ISSN: 0006-8993 [Print] Netherlands
PMID2539878 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Bridged Bicyclo Compounds
  • Bridged Bicyclo Compounds, Heterocyclic
  • Chlorides
  • Receptors, GABA-A
  • Picrotoxin
  • Muscimol
  • tert-butylbicyclophosphorothionate
  • Pentobarbital
Topics
  • Animals
  • Bridged Bicyclo Compounds (metabolism)
  • Bridged Bicyclo Compounds, Heterocyclic
  • Chlorides (physiology)
  • Dose-Response Relationship, Drug
  • Frontal Lobe (physiopathology)
  • Male
  • Mice
  • Mice, Inbred BALB C (physiology)
  • Mice, Inbred DBA (physiology)
  • Muscimol (metabolism)
  • Pentobarbital (pharmacology)
  • Picrotoxin
  • Receptors, GABA-A (drug effects, physiology)
  • Seizures (chemically induced, physiopathology)
  • Species Specificity
  • Synaptosomes (physiology)

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