Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum

GOMEZ G; CADET JL; GONZALEZ B; BISAGNO V; GARCIA-RILL E; GONZALEZ B; MUÑIZ JA; GARCIA-RILL E; RIVERO ECHETO MC; URBANO FJ; MUÑIZ JA; RIVERO ECHETO MC; URBANO FJ; GOMEZ G; CADET JL; BISAGNO V

NEUROTOXICITY RESEARCH

SPRINGER

Lugar: Berlin; Año: 2016 vol. 29 p. 525 - 538

1029-8428

Caffeine is the world´s most popular psychoactive drug and is also an active adulterant found in many drugs of abuse, including seized cocaine samples. Despite several studies which examine the effects of caffeine or cocaine administered as single agents, little data are available for these agents when given in combination. The purpose of the present study was to determine if combined intake of both psychostimulants can lead to maladaptive changes in striatal function. Mice were injected with a binge regimen (intermittent treatment for 13 days) of caffeine (3 × 5 mg/kg), cocaine (3 × 10 mg/kg), or combined administration. We found that chronic caffeine potentiated locomotion induced by cocaine and that both caffeine-treated groups showed sensitization. Striatal tissue was obtained 24 h and 7 days after last injection (withdrawal) for immunohistochemistry and mRNA expression. Our results show that combined intake of both psychostimulants can increase GFAP immunoreactivity in the striatum at both times post treatment. Gene expression analysis, targeted at dopamine, adenosine, and glutamate receptor subunit genes, revealed significant transcript down-regulation in the dorsal striatum of AMPA, NMDA, D1 and D2 receptor subunit mRNA expression in the group that received combined treatment, but not after individual administration. At withdrawal, we found increased D1 receptor mRNA expression along with increased A1, AMPA, NMDA, and metabotropic subunit expression. A2A mRNA showed decreased expression after both times in all experimental groups. Our study provides evidence that there are striatal alterations mediated by combined caffeine and cocaine administration, and highlights negative outcomes of chronic intake of both psychostimulants.