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Caffeine intake exerts dual genome-wide effects on hippocampal metabolism and learning-dependent transcription

Caffeine is the most widely consumed psychoactive substance in the world. Strikingly, the molecular pathways engaged by its regular consumption remain unclear. We herein addressed the mechanisms associated with habitual (chronic) caffeine consumption in the mouse hippocampus using untargeted orthogo...

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Bibliographic Details
Published in:The Journal of clinical investigation 2022-06, Vol.132 (12), p.1-16
Main Authors: Paiva, Isabel, Cellai, Lucrezia, Meriaux, Céline, Poncelet, Lauranne, Nebie, Ouada, Saliou, Jean-Michel, Lacoste, Anne-Sophie, Papegaey, Anthony, Drobecq, Hervé, Le Gras, Stéphanie, Schneider, Marion, Malik, Enas M, Müller, Christa E, Faivre, Emilie, Carvalho, Kevin, Gomez-Murcia, Victoria, Vieau, Didier, Thiroux, Bryan, Eddarkaoui, Sabiha, Lebouvier, Thibaud, Schueller, Estelle, Tzeplaeff, Laura, Grgurina, Iris, Seguin, Jonathan, Stauber, Jonathan, Lopes, Luisa V, Buée, Luc, Buée-Scherrer, Valérie, Cunha, Rodrigo A, Ait-Belkacem, Rima, Sergeant, Nicolas, Annicotte, Jean-Sébastien, Boutillier, Anne-Laurence, Blum, David
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Language:English
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Summary:Caffeine is the most widely consumed psychoactive substance in the world. Strikingly, the molecular pathways engaged by its regular consumption remain unclear. We herein addressed the mechanisms associated with habitual (chronic) caffeine consumption in the mouse hippocampus using untargeted orthogonal omics techniques. Our results revealed that chronic caffeine exerts concerted pleiotropic effects in the hippocampus at the epigenomic, proteomic, and metabolomic levels. Caffeine lowered metabolism-related processes (e.g., at the level of metabolomics and gene expression) in bulk tissue, while it induced neuron-specific epigenetic changes at synaptic transmission/plasticity-related genes and increased experience-driven transcriptional activity. Altogether, these findings suggest that regular caffeine intake improves the signal-to-noise ratio during information encoding, in part through fine-tuning of metabolic genes, while boosting the salience of information processing during learning in neuronal circuits.
ISSN:1558-8238
0021-9738
1558-8238
DOI:10.1172/JCI149371