Antagonism of isoniazid-induced convulsions by abecarnil in mice tolerant to diazepam

Pharmacol Biochem Behav. 1995 Oct;52(2):249-54. doi: 10.1016/0091-3057(94)00422-f.

Abstract

The ability of the benzodiazepine receptor full agonist diazepam, the selective agonist abecarnil, and the partial agonist imidazenil to antagonize convulsions induced by isoniazid (200 mg/kg, S.C.) was studied in mice chronically treated with diazepam (3 mg/kg, i.p., three times daily) or abecarnil (0.1 or 1 mg/kg, i.p., three times daily or 6 mg/kg, S.C., daily). Diazepam induced tolerance to its own anticonvulsant effect. In contrast, chronic treatment with abecarnil failed to induce tolerance to its own anticonvulsant activity. Animals treated with abecarnil at 0.1 mg/kg developed cross-tolerance to imidazenil, whereas those treated with 1 mg/kg became less sensitive to diazepam. Mice chronically treated with abecarnil at 6 mg/kg showed almost complete tolerance to diazepam. Abecarnil was able to antagonize the convulsions elicited by isoniazid in diazepam-tolerant mice. These data indicate that chronic administration of abecarnil, unlike that of classical benzodiazepines, does not induce tolerance to its anticonvulsant effect, and that abecarnil overcomes tolerance induced by long-term treatment with the full agonist diazepam.

MeSH terms

  • Animals
  • Anticonvulsants / pharmacology*
  • Benzodiazepines / pharmacology
  • Carbolines / pharmacology*
  • Convulsants / antagonists & inhibitors*
  • Convulsants / pharmacology
  • Diazepam / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Tolerance
  • GABA Modulators / pharmacology
  • Imidazoles / pharmacology
  • Isoniazid / antagonists & inhibitors*
  • Isoniazid / pharmacology
  • Male
  • Mice
  • Seizures / chemically induced
  • Seizures / prevention & control*

Substances

  • Anticonvulsants
  • Carbolines
  • Convulsants
  • GABA Modulators
  • Imidazoles
  • Benzodiazepines
  • imidazenil
  • abecarnil
  • Diazepam
  • Isoniazid