Alterations of physostigmine-induced yawning by chronic lithium administration in rats

Pharmacol Toxicol. 1997 Oct;81(4):159-63. doi: 10.1111/j.1600-0773.1997.tb02062.x.

Abstract

The effect of chronic lithium pretreatment on physostigmine-induced yawning was investigated in male rats. Intraperitoneal administration of physostigmine to rats induced yawning in a biphasic manner. However the maximum response was obtained by 0.2 mg/kg of the drug. Intracerebroventricular administrations of a putative M1 and M2 muscarinic receptor antagonists, pirenzepine and methoctramine decreased physostigmine-induced yawning. Intraperitoneal administration of a non-selective muscarinic receptor antagonist, atropine, also decreased the physostigmine-induced yawning significantly. Chronic lithium pretreatment (30 days) reduced yawning induced by physostigmine. The inhibitory effect of pirenzepine, methoctramine and atropine on physostigmine-induced yawning increased in rats pretreated with chronic lithium. These findings indicate that yawning is induced by a central cholinergic mechanism and that chronic pretreatment of lithium may interact with the cholinergic-induced behaviour.

MeSH terms

  • Animals
  • Antimanic Agents / pharmacology*
  • Atropine / pharmacology
  • Diamines / administration & dosage
  • Diamines / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Injections, Intraperitoneal
  • Injections, Intraventricular
  • Lithium Chloride / administration & dosage
  • Lithium Chloride / pharmacology*
  • Male
  • Muscarinic Antagonists / pharmacology*
  • Parasympatholytics / pharmacology
  • Physostigmine / administration & dosage*
  • Pirenzepine / administration & dosage
  • Pirenzepine / pharmacology
  • Rats
  • Yawning / drug effects*

Substances

  • Antimanic Agents
  • Diamines
  • Muscarinic Antagonists
  • Parasympatholytics
  • Pirenzepine
  • Atropine
  • Physostigmine
  • Lithium Chloride
  • methoctramine