Receptor and metabolic insights on the ability of caffeine to prevent alcohol-induced stimulation of mesolimbic dopamine transmission

Bassareo V.

Member of the Collaboration Group

;Maccioni R.

Member of the Collaboration Group

;Talani G.

Member of the Collaboration Group

;Zuffa S.

Member of the Collaboration Group

;El Abiead Y.

Member of the Collaboration Group

;Lorrai I.

Member of the Collaboration Group

;Kawamura T.

Member of the Collaboration Group

;Pantis S.

Member of the Collaboration Group

;Puliga R.

Member of the Collaboration Group

;Vargiu R.

Member of the Collaboration Group

;Lecca D.;Enrico P.;Peana A.;Dazzi L.;Dorrestein P. C.

Member of the Collaboration Group

;Sanna P. P.

Member of the Collaboration Group

;Sanna E.

Member of the Collaboration Group

;Acquas E.

Member of the Collaboration Group

2024-01-01

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Abstract

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 A2A adenosine receptors (A2AR), prevents alcohol-dependent activation of mesolimbic DA function as assessed, in-vivo, by brain microdialysis of AcbSh DA and, in-vitro, by electrophysiological recordings of pVTA DA neuronal firing. Accordingly, while the A1R antagonist DPCPX fails to prevent the effects of alcohol on DA function, both caffeine and the A2AR antagonist SCH 58261 prevent alcohol-dependent pVTA generation of salsolinol and increase in AcbSh DA in-vivo, as well as alcohol-dependent excitation of pVTA DA neurons in-vitro. However, caffeine also prevents direct salsolinol- and morphine-stimulated DA function, suggesting that it can exert these inhibitory effects also independently from affecting alcohol-induced salsolinol formation or bioavailability. Finally, untargeted metabolomics of the pVTA showcases that caffeine antagonizes alcohol-mediated effects on molecules (e.g. phosphatidylcholines, fatty amides, carnitines) involved in lipid signaling and energy metabolism, which could represent an additional salsolinol-independent mechanism of caffeine in impairing alcohol-mediated stimulation of mesolimbic DA transmission. In conclusion, the outcomes of this study strengthen the potential of caffeine, as well as of A2AR antagonists, for future development of preventive/therapeutic strategies for alcohol use disorder.