Locomotor activity in mice during chronic treatment with caffeine and withdrawal

Pharmacol Biochem Behav. 1993 Jan;44(1):199-216. doi: 10.1016/0091-3057(93)90299-9.

Abstract

Chronic ingestion of caffeine by mice caused a marked reduction in locomotor exploratory activity. At least 4 days of withdrawal were required to restore activity to normal levels. Stimulatory effects of injected caffeine were lower in chronically treated mice and the biphasic dose-response (stimulatory followed by depressant) curve for injected caffeine was left shifted. Seven days of withdrawal were required before the dose-response curve to caffeine was identical to that of control mice. The depressant effects of a potent xanthine phosphodiesterase inhibitor, 1,3-dipropyl-7-methylxanthine, were blunted in caffeine-treated mice. The depressant effects of A1- and A2-selective adenosine analogs were enhanced after chronic caffeine. There was little or no effect of chronic caffeine on the stimulatory effects of dopaminergic agents (amphetamine, caffeine), while both depressant and stimulatory effects of cholinergic agents (nicotine, oxotremorine, scopolamine) were reduced. The results indicate that chronic caffeine affects functions of adenosine and cholinergic receptors related to regulation of locomotor exploratory activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • Adenosine / pharmacology
  • Animals
  • Caffeine / pharmacology*
  • Dopamine Agents / pharmacology
  • Dose-Response Relationship, Drug
  • Male
  • Mice
  • Motor Activity / drug effects*
  • Parasympathomimetics / pharmacology
  • Substance Withdrawal Syndrome / physiopathology*
  • Xanthines / pharmacology

Substances

  • Dopamine Agents
  • Parasympathomimetics
  • Xanthines
  • 1,3-dipropyl-7-methylxanthine
  • Caffeine
  • Adenosine
  • 1-Methyl-3-isobutylxanthine