Hypothalamic neurotensin projections promote reward by enhancing glutamate transmission in the VTA

The lateral hypothalamus (LH) sends a dense glutamatergic and peptidergic projection to dopamine neurons in the ventral tegmental area (VTA), a cell group known to promote reinforcement and aspects of reward. The role of the LH to VTA projection in reward-seeking behavior can be informed by using op...

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Published inThe Journal of neuroscience Vol. 33; no. 18; pp. 7618 - 7626
Main Authors Kempadoo, Kimberly A, Tourino, Clara, Cho, Saemi L, Magnani, Francesco, Leinninger, Gina-Marie, Stuber, Garret D, Zhang, Feng, Myers, Martin G, Deisseroth, Karl, de Lecea, Luis, Bonci, Antonello
Format Journal Article
LanguageEnglish
Published United States Society for Neuroscience 01.05.2013
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Summary:The lateral hypothalamus (LH) sends a dense glutamatergic and peptidergic projection to dopamine neurons in the ventral tegmental area (VTA), a cell group known to promote reinforcement and aspects of reward. The role of the LH to VTA projection in reward-seeking behavior can be informed by using optogenetic techniques to dissociate the actions of LH neurons from those of other descending forebrain inputs to the VTA. In the present study, we identify the effect of neurotensin (NT), one of the most abundant peptides in the LH to VTA projection, on excitatory synaptic transmission in the VTA and reward-seeking behavior. Mice displayed robust intracranial self-stimulation of LH to VTA fibers, an operant behavior mediated by NT 1 receptors (Nts1) and NMDA receptors. Whole-cell patch-clamp recordings of VTA dopamine neurons demonstrated that NT (10 nm) potentiated NMDA-mediated EPSCs via Nts1. Results suggest that NT release from the LH into the VTA activates Nts1, thereby potentiating NMDA-mediated EPSCs and promoting reward. The striking behavioral and electrophysiological effects of NT and glutamate highlight the LH to VTA pathway as an important component of reward.
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K.A. Kempadoo's present address: Columbia University, 1051 Riverside Drive, Kolb Annex Unit 87, New York, NY 10032.
Author contributions: K.A.K., C.T., and A.B. designed research; K.A.K., C.T., S.L.C., and F.M. performed research; G.-M.L., G.D.S., F.Z., M.G.M., K.D., and L.d.L. contributed unpublished reagents/analytic tools; K.A.K. analyzed data; K.A.K. wrote the paper.
A. Bonci's present address: Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892.
ISSN:0270-6474
1529-2401
1529-2401
DOI:10.1523/JNEUROSCI.2588-12.2013