Evidence map›Paper›PMID 23700406›Full record

Trial reportPloS one2013

Treatment of obesity and diabetes using oxytocin or analogs in patients and mouse models.

Hai Zhang, Chenguang Wu, Qiaofen Chen, Xiaoluo Chen, Zhigang Xu, Jing Wu, Dongsheng Cai

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

121 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Effects of Intranasal Oxytocin on the Blood Oxygenation Level-Dependent Signal in Food Motivation and Cognitive Control Pathways in Overweight and Obese Men.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Trial
  12. Trial
  13. Oxytocin reduces caloric intake in men.Obesity (Silver Spring, Md.) · 2015
    Trial
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. The serum oxytocin correlated with serum leptin and body mass index in Japanese adolescents.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2026
    Article
  20. Review

61 more citing papers are in PubMed but not listed here.

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

7 authors.

Hai ZhangDepartment of Molecular Pharmacology, Diabetes Research Center, Institute of Aging, Albert Einstein College of Medicine, Bronx, New York, USA.
Chenguang Wu
Qiaofen Chen
Xiaoluo Chen
Zhigang Xu
Jing Wu
Dongsheng Cai

Funding

The Hypothalamic Basis of AgingR01AG031774 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Dongsheng Cai · 2010 to 2026
$6.3M
Role of IKK-Beta/NF-KappaB in Hypothalamic Dysregulation of Energy BalanceR01DK078750 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI CAI, DONGSHENG · 2008 to 2017
$3.8M
NIA NIH HHS R01 AG031774NIDDK NIH HHS R01 DK078750
6 · The paper itself

Abstract

Obesity is important for the development of type-2 diabetes as a result of obesity-induced insulin resistance accompanied by impaired compensation of insulin secretion from pancreatic beta cells. Here, based on a randomized pilot clinical trial, we report that intranasal oxytocin administration over an 8-week period led to effective reduction of obesity and reversal of related prediabetic changes in patients. Using mouse models, we further systematically evaluated whether oxytocin and its analogs yield therapeutic effects against prediabetic or diabetic disorders regardless of obesity. Our results showed that oxytocin and two analogs including [Ser4, Ile8]-oxytocin or [Asu1,6]-oxytocin worked in mice to reverse insulin resistance and glucose intolerance prior to reduction of obesity. In parallel, using streptozotocin-induced diabetic mouse model, we found that treatment with oxytocin or its analogs reduced the magnitude of glucose intolerance through improving insulin secretion. The anti-diabetic effects of oxytocin and its analogs in these animal models can be produced similarly whether central or peripheral administration was used. In conclusion, oxytocin and its analogs have multi-level effects in improving weight control, insulin sensitivity and insulin secretion, and bear potentials for being developed as therapeutic peptides for obesity and diabetes.

Indexed as

Administration, IntranasalAdultAnimalsBlood GlucoseDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2FemaleGlucose IntoleranceHumansHypoglycemic AgentsInsulinInsulin ResistanceInsulin SecretionLipid MetabolismMaleMiceBlood GlucoseHypoglycemic AgentsInsulinisotocinOxytocinoxytocin, 1,6-alpha-Asu-

Identifiers

PMID23700406
PMCPMC3658979

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.