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Arousal effect of caffeine depends on adenosine A2A receptors in the shell of the nucleus accumbens
- Source :
- The Journal of neuroscience : the official journal of the Society for Neuroscience. 31(27)
- Publication Year :
- 2011
-
Abstract
- Caffeine, the most widely used psychoactive compound, is an adenosine receptor antagonist. It promotes wakefulness by blocking adenosine A(2A) receptors (A(2A)Rs) in the brain, but the specific neurons on which caffeine acts to produce arousal have not been identified. Using selective gene deletion strategies based on the Cre/loxP technology in mice and focal RNA interference to silence the expression of A(2A)Rs in rats by local infection with adeno-associated virus carrying short-hairpin RNA, we report that the A(2A)Rs in the shell region of the nucleus accumbens (NAc) are responsible for the effect of caffeine on wakefulness. Caffeine-induced arousal was not affected in rats when A(2A)Rs were focally removed from the NAc core or other A(2A)R-positive areas of the basal ganglia. Our observations suggest that caffeine promotes arousal by activating pathways that traditionally have been associated with motivational and motor responses in the brain.
- Subjects :
- Receptor, Adenosine A2A
Green Fluorescent Proteins
Poison control
Adenosine A2A receptor
Mice, Transgenic
Nucleus accumbens
Pharmacology
Adenosine receptor antagonist
Transfection
Basal Ganglia
Nucleus Accumbens
Article
Choline O-Acetyltransferase
Rats, Sprague-Dawley
chemistry.chemical_compound
Mice
Caffeine
Basal ganglia
Animals
Humans
RNA, Small Interfering
Receptor
Cell Line, Transformed
Mice, Knockout
Analysis of Variance
Dose-Response Relationship, Drug
Electromyography
Receptors, Dopamine D2
General Neuroscience
Electroencephalography
Rats
Mice, Inbred C57BL
chemistry
Mutagenesis
Phosphopyruvate Hydratase
Mutation
Wakefulness
Central Nervous System Stimulants
Arousal
Locomotion
Subjects
Details
- ISSN :
- 15292401
- Volume :
- 31
- Issue :
- 27
- Database :
- OpenAIRE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Accession number :
- edsair.doi.dedup.....6b8d1a0e79cd951508a22445a4225d67