Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 May 1:167:108005.
doi: 10.1016/j.neuropharm.2020.108005. Epub 2020 Feb 11.

Neurotensin in reward processes

Affiliations
Review

Neurotensin in reward processes

María Luisa Torruella-Suárez et al. Neuropharmacology. .

Abstract

Neurotensin (NTS) is a neuropeptide neurotransmitter expressed in the central and peripheral nervous systems. Many studies over the years have revealed a number of roles for this neuropeptide in body temperature regulation, feeding, analgesia, ethanol sensitivity, psychosis, substance use, and pain. This review provides a general survey of the role of neurotensin with a focus on modalities that we believe to be particularly relevant to the study of reward. We focus on NTS signaling in the ventral tegmental area, nucleus accumbens, lateral hypothalamus, bed nucleus of the stria terminalis, and central amygdala. Studies on the role of NTS outside of the ventral tegmental area are still in their relative infancy, yet they reveal a complex role for neurotensinergic signaling in reward-related behaviors that merits further study. This article is part of the special issue on 'Neuropeptides'.

Keywords: Alcohol; Dopamine; Feeding; NTSR1; NTSR2; Neurotensin; Reward; Substance use disorder.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Circuit diagram outlining regions where NTS and NTSR1 are expressed, physiological ramifications of NTS signaling, and behaviors mediated by these circuits. Lateral hypothalamus (LH), medial preoptic area (mPOA), central nucleus of the amgydala (CeA), ventral tegmental area (VTA), bed nucleus of the stria terminalis (BNST), parabrachial nucleus (PBN), nucleus accumbens (NA). Light blue = NTS neurons and projections, dark blue = NTSR1 expressing neurons, green = dopamine neurons and projections.

References

    1. Amano T, Wada E, Yamada D, Zushida K, Maeno H, Noda M, Wada K, Sekiguchi M, 2008. Heightened Amygdala Long-Term Potentiation in Neurotensin Receptor Type-1 Knockout Mice. Neuropsychopharmacology 33, 3135–3145. 10.1038/npp.2008.38 - DOI - PubMed
    1. Arluison M, Brochier G, Vankova M, Leviel V, Villalobos J, Tramu G, 1994. Demonstration of peptidergic afferents to the bed nucleus of the stria terminalis using local injections of colchicine. A combined immunohistochemical and retrograde tracing study. Brain Res. Bull 34, 319–337. 10.1016/0361-9230(94)90026-4 - DOI - PubMed
    1. Bédard A-M, Maheux J, Lévesque D, Samaha A-N, 2011. Continuous, but not Intermittent, Antipsychotic Drug Delivery Intensifies the Pursuit of Reward Cues. Neuropsychopharmacology 36, 1248–1259. 10.1038/npp.2011.10 - DOI - PMC - PubMed
    1. Besserer-Offroy É, Brouillette RL, Lavenus S, Froehlich U, Brumwell A, Murza A, Longpré J-M, Marsault É, Grandbois M, Sarret P, Leduc R, 2017. The signaling signature of the neurotensin type 1 receptor with endogenous ligands. Eur. J. Pharmacol 805, 1–13. 10.1016/j.ejphar.2017.03.046 - DOI - PubMed
    1. Betancur C, 2001. Neurotensin Gene Expression and Behavioral Responses Following Administration of Psychostimulants and Antipsychotic Drugs in Dopamine D3 Receptor Deficient Mice. Neuropsychopharmacology 24, 170–182. 10.1016/S0893133X(00)00179-2 - DOI - PMC - PubMed

Publication types