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Cansell, C.* ; Castel, J.* ; Denis, R.G.* ; Rouch, C.* ; Delbes, A.S.* ; Martinez, S.* ; Mestivier, D.* ; Finan, B. ; Maldonado-Aviles, J.G.* ; Rijnsburger, M.* ; Tschöp, M.H. ; Dileone, R.J.* ; Eckel, R.H.* ; la Fleur, S.E.* ; Magnan, C.* ; Hnasko, T.S.* ; Luquet, S.*

Dietary triglycerides act on mesolimbic structures to regulate the rewarding and motivational aspects of feeding.

Mol. Psychiatry 19, 1095-1105 (2014)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Circulating triglycerides (TGs) normally increase after a meal but are altered in pathophysiological conditions, such as obesity. Although TG metabolism in the brain remains poorly understood, several brain structures express enzymes that process TG-enriched particles, including mesolimbic structures. For this reason, and because consumption of high-fat diet alters dopamine signaling, we tested the hypothesis that TG might directly target mesolimbic reward circuits to control reward-seeking behaviors. We found that the delivery of small amounts of TG to the brain through the carotid artery rapidly reduced both spontaneous and amphetamine-induced locomotion, abolished preference for palatable food and reduced the motivation to engage in food-seeking behavior. Conversely, targeted disruption of the TG-hydrolyzing enzyme lipoprotein lipase specifically in the nucleus accumbens increased palatable food preference and food-seeking behavior. Finally, prolonged TG perfusion resulted in a return to normal palatable food preference despite continued locomotor suppression, suggesting that adaptive mechanisms occur. These findings reveal new mechanisms by which dietary fat may alter mesolimbic circuit function and reward seeking.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Nervous-system Control; Fatty-acid-metabolism; Food-intake; Lipoprotein-lipase; Energy-balance; Insulin-secretion; Dorsal Striatum; Brain Dopamine; Obesity; Expression
Sprache
Veröffentlichungsjahr 2014
HGF-Berichtsjahr 2014
ISSN (print) / ISBN 1359-4184
e-ISSN 1476-5578
Zeitschrift Molecular Psychiatry
Quellenangaben Band: 19, Heft: 10, Seiten: 1095-1105 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Obesity (IDO)
German Center for Diabetes Reseach (DZD)
POF Topic(s) 30201 - Metabolic Health
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502200-001
Scopus ID 84897967203
PubMed ID 24732670
Erfassungsdatum 2014-04-17