The 5-HT3 antagonist MDL-72222 exacerbates ethanol withdrawal seizures in mice

Alcohol Clin Exp Res. 1994 Apr;18(2):410-4. doi: 10.1111/j.1530-0277.1994.tb00034.x.

Abstract

Ethanol-dependent mice were treated with the 5-HT3 antagonist MDL 72222 after withdrawal from ethanol. Treatment with unit doses (0, 5.6, 10, and 17.0 mg/kg) of MDL 72222 at 0, 4, and 7 hr after withdrawal dose-dependently exacerbated the severity of ethanol withdrawal seizures. Treatment with a single dose (17 mg/kg) of MDL 72222 at 5 hr after withdrawal also exacerbated the severity of ethanol withdrawal seizures. Ethanol naive mice treated with MDL 72222 (56 mg/kg) did not display any seizures. Treatment with another 5-HT3 antagonist, ICS 205-930 (23 and 46 mg/kg), or the 5-HT2 receptor antagonist ketanserin, did not affect ethanol withdrawal seizures. The findings suggest MDL 72222 selectively enhances sensitivity to withdrawal seizures following chronic ethanol exposure.

Publication types

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

MeSH terms

  • Alcohol Withdrawal Delirium / physiopathology*
  • Animals
  • Dose-Response Relationship, Drug
  • Electroencephalography / drug effects*
  • Evoked Potentials / drug effects
  • Evoked Potentials / physiology
  • Ketanserin / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Postural Balance / drug effects
  • Postural Balance / physiology
  • Receptors, Serotonin / classification
  • Receptors, Serotonin / drug effects*
  • Receptors, Serotonin / physiology
  • Seizures / physiopathology*
  • Serotonin Antagonists / pharmacology*
  • Stimulation, Chemical
  • Tropanes / pharmacology*

Substances

  • Receptors, Serotonin
  • Serotonin Antagonists
  • Tropanes
  • Ketanserin
  • bemesetron