Potentiation of amphetamine-mediated responses in caffeine-sensitized rats involves modifications in A2A receptors and zif-268 mRNAs in striatal neurons

J Neurochem. 2006 Aug;98(4):1078-89. doi: 10.1111/j.1471-4159.2006.03943.x. Epub 2006 Jun 12.

Abstract

Subchronic intermittent administration of caffeine induces sensitization of motor behaviour and promotes cross-sensitization to amphetamine motor activity. In order to evaluate the possible mechanisms at the basis of these effects, modifications in A(2A) receptor and zif-268 mRNAs were evaluated in rats subchronically treated with caffeine (15 mg/kg i.p.) and challenged with caffeine (15 mg/kg i.p.) or amphetamine (0.5, 1 mg/kg s.c.) 3 days after discontinuation of treatment. Results showed that the sensitized motor response to caffeine was associated with a decrease of adenosine A(2A) receptor and zif-268 mRNA levels in the striatum and nucleus accumbens, whereas cross-sensitization to amphetamine was linked to a more pronounced increase of zif-268 mRNA levels in the striatum, but not in the nucleus accumbens. Single-cell analysis showed that zif-268 mRNA modifications occurred in Enk(+) striatopallidal neurons after acute or subchronic treatment with caffeine and in Enk(-) striatonigral neurons after acute amphetamine administration. Potentiation of amphetamine effects was not associated with modifications of amphetamine-induced dopamine release in nucleus accumbens in caffeine-pretreated rats compared with vehicle-pretreated rats. Results demonstrate that sensitization to caffeine and cross-sensitization to amphetamine are associated with post-synaptic neuroadaptive changes in selective neuronal populations of the striatum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamine / pharmacology*
  • Animals
  • Autoradiography
  • Caffeine / pharmacology*
  • Central Nervous System Stimulants / pharmacology*
  • Dopamine / metabolism
  • Drug Synergism
  • In Situ Hybridization
  • Male
  • Microdialysis
  • Motor Activity / drug effects
  • Neostriatum / cytology
  • Neostriatum / drug effects
  • Neostriatum / metabolism*
  • Neurons / drug effects
  • Neurons / metabolism*
  • Nucleus Accumbens / metabolism
  • RNA, Messenger / biosynthesis*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Adenosine A2A / drug effects*
  • Receptors, Dopamine D2 / biosynthesis
  • Synapses / metabolism

Substances

  • Central Nervous System Stimulants
  • RNA, Messenger
  • Receptor, Adenosine A2A
  • Receptors, Dopamine D2
  • Caffeine
  • Amphetamine
  • Dopamine