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Berland, C. ; Montalban, E.* ; Perrin, E.* ; Di Miceli, M.* ; Nakamura, Y.* ; Martinat, M.* ; Sullivan, M.* ; Davis, X.S.* ; Shenasa, M.A.* ; Martin, C.* ; Tolu, S.* ; Marti, F.* ; Caille, S.* ; Castel, J.* ; Perez, S.* ; Salinas, C.G.* ; Morel, C.* ; Hecksher-Sørensen, J.* ; Cador, M.* ; Fioramonti, X.* ; Tschöp, M.H. ; Layé, S.* ; Venance, L.* ; Faure, P.* ; Hnasko, T.S.* ; Small, D.M.* ; Gangarossa, G.* ; Luquet, S.H.*

Circulating triglycerides gate dopamine-associated behaviors through DRD2-expressing neurons.

Cell Metab. 31, 773-790 (2020)
Postprint Forschungsdaten DOI PMC
Open Access Green
Energy-dense food alters dopaminergic (DA) transmission in the mesocorticolimbic (MCL) system and can promote reward dysfunctions, compulsive feeding, and weight gain. Yet the mechanisms by which nutrients influence the MCL circuitry remain elusive. Here, we show that nutritional triglycerides (TGs), a conserved post-prandial metabolic signature among mammals, can be metabolized within the MCL system and modulate DA-associated behaviors by gating the activity of dopamine receptor subtype 2 (DRD2)-expressing neurons through a mechanism that involves the action of the lipoprotein lipase (LPL). Further, we show that in humans, postprandial TG excursions modulate brain responses to food cues in individuals carrying a genetic risk for reduced DRD2 signaling. Collectively, these findings unveil a novel mechanism by which dietary TGs directly alter signaling in the reward circuit to regulate behavior, thereby providing a new mechanistic basis by which energy-rich diets may lead to (mal)adaptations in DA signaling that underlie reward deficit and compulsive behavior.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Dopamine ; Dopamine Receptor D2 ; Fmri ; Food-reward ; Lipoprotein Lipase ; Nucleus Accumbens ; Striatum ; Triglycerides ; Ventral Tegmental Area; High-fat Diet; Lipoprotein-lipase; Nucleus-accumbens; Receptor Gene; D2 Receptors; Energy-balance; Weight-gain; Food-intake; Long-term; Brain
Sprache englisch
Veröffentlichungsjahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 1550-4131
e-ISSN 1932-7420
Zeitschrift Cell Metabolism
Quellenangaben Band: 31, Heft: 4, Seiten: 773-790 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort 50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Obesity (IDO)
POF Topic(s) 30201 - Metabolic Health
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502200-001
DOI 10.1016/j.cmet.2020.02.010
WOS ID WOS:000524972800014
Scopus ID 85082749377
PubMed ID 32142669
Erfassungsdatum 2020-04-29
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