No modifications of GABAA and benzodiazepine receptors following experimental dysthyroidism in rats

Pharmacol Res. 1993 Jul-Aug;28(1):47-52. doi: 10.1006/phrs.1993.1108.

Abstract

The effect of a treatment with L-triiodothyronine (T3) or propylthiouracil (PTU) on the characteristics of benzodiazepine and chloride ion channel binding sites in rat hippocampus and cerebral cortex was studied using a radiolabelled technique. In our experimental conditions, neither hyper- nor hypothyroidism modified number and affinity of [3H]flunitrazepam or [3H]butylbicycloorthobenzoate (TBOB) binding sites. These data indicate that neither benzodiazepine nor chloride ionophore sites of the GABA complex are modified in an experimental condition of dysthyroidism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cerebral Cortex / drug effects
  • Chloride Channels / metabolism
  • Disease Models, Animal
  • Hippocampus / drug effects
  • Hyperthyroidism / chemically induced
  • Hyperthyroidism / metabolism*
  • Hypothyroidism / chemically induced
  • Hypothyroidism / metabolism*
  • Male
  • Propylthiouracil
  • Rats
  • Rats, Wistar
  • Receptors, GABA-A / metabolism*
  • Triiodothyronine
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • Chloride Channels
  • Receptors, GABA-A
  • Triiodothyronine
  • gamma-Aminobutyric Acid
  • Propylthiouracil