Receptor and metabolic insights on the ability of caffeine to prevent alcohol-induced stimulation of mesolimbic dopamine transmission.
Animals
Caffeine
/ pharmacology
Dopamine
/ metabolism
Ethanol
/ pharmacology
Male
Ventral Tegmental Area
/ drug effects
Nucleus Accumbens
/ drug effects
Dopaminergic Neurons
/ drug effects
Rats
Receptor, Adenosine A2A
/ metabolism
Synaptic Transmission
/ drug effects
Adenosine A2 Receptor Antagonists
/ pharmacology
Isoquinolines
Journal
Translational psychiatry
ISSN: 2158-3188
Titre abrégé: Transl Psychiatry
Pays: United States
ID NLM: 101562664
Informations de publication
Date de publication:
28 Sep 2024
28 Sep 2024
Historique:
received:
13
08
2024
accepted:
23
09
2024
revised:
19
09
2024
medline:
29
9
2024
pubmed:
29
9
2024
entrez:
28
9
2024
Statut:
epublish
Résumé
The consumption of alcohol and caffeine affects the lives of billions of individuals worldwide. Although recent evidence indicates that caffeine impairs the reinforcing properties of alcohol, a characterization of its effects on alcohol-stimulated mesolimbic dopamine (DA) function was lacking. Acting as the pro-drug of salsolinol, alcohol excites DA neurons in the posterior ventral tegmental area (pVTA) and increases DA release in the nucleus accumbens shell (AcbSh). Here we show that caffeine, via antagonistic activity on A
Identifiants
pubmed: 39341817
doi: 10.1038/s41398-024-03112-6
pii: 10.1038/s41398-024-03112-6
doi:
Substances chimiques
Caffeine
3G6A5W338E
Dopamine
VTD58H1Z2X
Ethanol
3K9958V90M
salsolinol
9ILS801M65
Receptor, Adenosine A2A
0
Adenosine A2 Receptor Antagonists
0
Isoquinolines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
391Subventions
Organisme : U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA)
ID : T32AA007456
Organisme : U.S. Department of Health & Human Services | National Institutes of Health (NIH)
ID : AA028982
Organisme : U.S. Department of Health & Human Services | National Institutes of Health (NIH)
ID : AA021667
Organisme : Regione Autonoma della Sardegna (Sardinia Region)
ID : RAS, CRP2_537-CUP F71J090006200002
Organisme : Fondazione Banco di Sardegna (Bank of Sardinia Foundation)
ID : Project ID F74I19000970007 (2018)
Informations de copyright
© 2024. The Author(s).
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