Evidence map›Paper›PMID 35192207›Full record

ReviewJournal of neuroendocrinology2022

Oxytocin as a potential pharmacological tool to combat obesity.

Pawel K Olszewski, Emily E Noble, Luis Paiva, Yoichi Ueta, James E Blevins

Open access · greenAbstract readReview
In one paragraph

Review in Journal of neuroendocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.8field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 5 institutions in 4 countries.

Pawel K OlszewskiFaculty of Science and Engineering, University of Waikato, Waikato, New Zealand.ORCID 0000-0002-2846-0485
Emily E NobleDepartment of Nutritional Sciences, University of Georgia, Athens, Georgia, USA.ORCID 0000-0002-7483-031X
Luis PaivaInstituto de Ciencia Animal, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, Valdivia, Chile.ORCID 0000-0003-3037-2756
Yoichi UetaDepartment of Physiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka, Japan.ORCID 0000-0003-0702-9538
James E BlevinsDepartment of Veterans Affairs Medical Center, VA Puget Sound Health Care System, Office of Research and Development Medical Research Service, Seattle, Washington, USA.ORCID 0000-0002-7587-0380
Austral University of Chile · CLUniversity of Georgia · USUniversity of Minnesota · USUniversity of Occupational and Environmental Health Japan · JPUniversity of Washington · US

Funding

Role of Brown Adipose Tissue Thermogenesis in Oxytocin-Elicited Weight LossR01DK115976 · NIDDK · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI BLEVINS, JAMES ERNEST · 2018 to 2021
$1.4M
Melanin-concentrating hormone and the neural regulation of feedingK01DK118000 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI NOBLE, EMILY ELIZABETH · 2019 to 2023
$769k
Role of Brown Adipose Tissue Thermogenesis in Oxytocin-Elicited Weight Loss in Rodents and Nonhuman PrimatesI01BX004102 · VA · VA PUGET SOUND HEALTHCARE SYSTEM · PI James Ernest Blevins · 2018 to 2026
–
BLRD VA I01 BX004102NIDDK NIH HHS K01 DK118000NIDDK NIH HHS R01 DK115976
6 · The paper itself

Abstract

The neuropeptide oxytocin (OT) has emerged as an important anorexigen in the regulation of food intake and energy balance. It has been shown that the release of OT and activation of hypothalamic OT neurons coincide with food ingestion. Its effects on feeding have largely been attributed to limiting meal size through interactions in key regulatory brain regions governing the homeostatic control of food intake such as the hypothalamus and hindbrain in addition to key feeding reward areas such as the nucleus accumbens and ventral tegmental area. Furthermore, the magnitude of an anorexigenic response to OT and feeding-related activation of the brain OT circuit are modified by the composition and flavor of a diet, as well as by a social context in which a meal is consumed. OT is particularly effective in reducing consumption of carbohydrates and sweet tastants. Pharmacologic, genetic, and pair-feeding studies indicate that OT-elicited weight loss cannot be fully explained by reductions of food intake and that the overall impact of OT on energy balance is also partly a result of OT-elicited changes in lipolysis, energy expenditure, and glucose regulation. Peripheral administration of OT mimics many of its effects when it is given into the central nervous system, raising the questions of whether and to what extent circulating OT acts through peripheral OT receptors to regulate energy balance. Although OT has been found to elicit weight loss in female mice, recent studies have indicated that sex and estrous cycle may impact oxytocinergic modulation of food intake. Despite the overall promising basic research data, attempts to use OT in the clinical setting to combat obesity and overeating have generated somewhat mixed results. The focus of this mini-review is to briefly summarize the role of OT in feeding and metabolism, address gaps and inconsistencies in our knowledge, and discuss some of the limitations to the potential use of chronic OT that should help guide future research on OT as a tailor-made anti-obesity therapeutic.

Indexed as

EatingOxytocinAnimalsCarbohydratesFemaleGlucoseMiceObesityReceptors, OxytocinWeight LossCarbohydratesGlucoseOxytocinReceptors, Oxytocinenergy expenditurefood intakemeal sizeobesityoxytocin

Identifiers

PMID35192207
PMCPMC9372234
OpenAlexW4211193576

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.