The Role of Central Neurotensin in Regulating Feeding and Body Weight.


Journal

Endocrinology
ISSN: 1945-7170
Titre abrégé: Endocrinology
Pays: United States
ID NLM: 0375040

Informations de publication

Date de publication:
01 05 2021
Historique:
received: 22 10 2020
pubmed: 19 2 2021
medline: 21 10 2021
entrez: 18 2 2021
Statut: ppublish

Résumé

The small peptide neurotensin (Nts) is implicated in myriad processes including analgesia, thermoregulation, reward, arousal, blood pressure, and modulation of feeding and body weight. Alterations in Nts have recently been described in individuals with obesity or eating disorders, suggesting that disrupted Nts signaling may contribute to body weight disturbance. Curiously, Nts mediates seemingly opposing regulation of body weight via different tissues. Peripherally acting Nts promotes fat absorption and weight gain, whereas central Nts signaling suppresses feeding and weight gain. Thus, because Nts is pleiotropic, a location-based approach must be used to understand its contributions to disordered body weight and whether the Nts system might be leveraged to improve metabolic health. Here we review the role of Nts signaling in the brain to understand the sites, receptors, and mechanisms by which Nts can promote behaviors that modify body weight. New techniques permitting site-specific modulation of Nts and Nts receptor-expressing cells suggest that, even in the brain, not all Nts circuitry exerts the same function. Intriguingly, there may be dedicated brain regions and circuits via which Nts specifically suppresses feeding behavior and weight gain vs other Nts-attributed physiology. Defining the central mechanisms by which Nts signaling modifies body weight may suggest strategies to correct disrupted energy balance, as needed to address overweight, obesity, and eating disorders.

Identifiants

pubmed: 33599716
pii: 6144574
doi: 10.1210/endocr/bqab038
pmc: PMC7951050
pii:
doi:

Substances chimiques

Receptors, Neurotensin 0
Neurotensin 39379-15-2

Types de publication

Journal Article Research Support, N.I.H., Extramural Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK020572
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK103808
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM092715
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM142521
Pays : United States

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society.

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Auteurs

Jariel Ramirez-Virella (J)

Neuroscience Program, Michigan State University, East Lansing, Michigan, USA.
Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, USA.

Gina M Leinninger (GM)

Neuroscience Program, Michigan State University, East Lansing, Michigan, USA.
Department of Physiology, Michigan State University, East Lansing, Michigan, USA.

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Classifications MeSH