Evidence map›Paper›PMID 23883680›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2013

High-protein diet selectively reduces fat mass and improves glucose tolerance in Western-type diet-induced obese rats.

Andreas Stengel, Miriam Goebel-Stengel, Lixin Wang, Eugenia Hu, Hiroshi Karasawa, Joseph R Pisegna, Yvette Taché

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% 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.

NCT01146704 nacompletednot on this map

Gastrointestinal Hormonal Regulation of Obesity

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2010 to 2019Enrolled31ConditionsObesityArmsProtein powder supplement, standard dosage based on 0.5 gram protein per pound of subject's lean body mass, Protein powder supplement, High Level Protein, based on 1 gram of protein per pound of lean body mass: 25% protein and 45% carbohydrate
NCT04812964 nacompletednot on this mapstarted 2018, after this paper: background citation

Modulation of the Intestinal Microbiome in Obesity by a High Protein Diet

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2018 to 2024Enrolled106ConditionsObesityArmsProtein powder supplement, standard dosage based on 0.5 gram protein per pound of subject's lean body mass, Protein powder supplement, High Level Protein, based on 1 gram of protein per pound of lean body mass: 25% protein and 45% carbohydrate
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. High-Protein Diet Combined WithFood science & nutrition · 2026
    Article
  2. Article
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  12. Fad diets and their effect on urinary stone formation.Translational andrology and urology · 2014
    Review
  13. Risk of postprandial insulin resistance: the liver/vagus rapport.Reviews in endocrine & metabolic disorders · 2014
    Review
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 at 2 institutions in 2 countries.

Andreas StengelCURE/Digestive Diseases Research Center, Center for Neurobiology of Stress, Department of Medicine, Digestive Diseases Division at the University of California Los Angeles, and VA Greater Los Angeles Health Care System, Los Angeles, California;
Miriam Goebel-Stengel
Lixin Wang
Eugenia Hu
Hiroshi Karasawa
Joseph R Pisegna
Yvette Taché
VA Greater Los Angeles Healthcare System · USUniversity of California, Los Angeles · US

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
Chronic stress mediates fat-related changes in insulin signaling and gut motilityRC1DK086150 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRADESI, SYLVIE, POTHOULAKIS, CHARALABOS · 2009 to 2010
$983k
NIDDK NIH HHS 5 RC1 DK086150-02NIDDK NIH HHS DK-41301
6 · The paper itself

Abstract

Obesity is an increasing health problem. Because drug treatments are limited, diets remain popular. High-protein diets (HPD) reduce body weight (BW), although the mechanisms are unclear. We investigated physiological mechanisms altered by switching diet induced obesity (DIO) rats from Western-type diet (WTD) to HPD. Male rats were fed standard (SD) or WTD (45% calories from fat). After developing DIO (50% of rats), they were switched to SD (15% calories from protein) or HPD (52% calories from protein) for up to 4 weeks. Food intake (FI), BW, body composition, glucose tolerance, insulin sensitivity, and intestinal hormone plasma levels were monitored. Rats fed WTD showed an increased FI and had a 25% greater BW gain after 9 wk compared with SD (P < 0.05). Diet-induced obese rats switched from WTD to HPD reduced daily FI by 30% on day 1, which lasted to day 9 (-9%) and decreased BW during the 2-wk period compared with SD/SD (P < 0.05). During these 2 wk, WTD/HPD rats lost 72% more fat mass than WTD/SD (P < 0.05), whereas lean mass was unaltered. WTD/HPD rats had lower blood glucose than WTD/SD at 30 min postglucose gavage (P < 0.05). The increase of pancreatic polypeptide and peptide YY during the 2-h dark-phase feeding was higher in WTD/HPD compared with WTD/SD (P < 0.05). These data indicate that HPD reduces BW in WTD rats, which may be related to decreased FI and the selective reduction of fat mass accompanied by improved glucose tolerance, suggesting relevant benefits of HPD in the treatment of obesity.

Indexed as

Glucose Tolerance TestAdiposityAnimalsBody WeightDietary ProteinsGlucoseMaleObesityRatsRats, Sprague-DawleyTreatment OutcomeDietary ProteinsGlucosediet-induced obesityfood intakegut hormoneshigh-protein diet

Identifiers

PMID23883680
PMCPMC3763043
OpenAlexW1976104403

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.