Evidence map›Paper›PMID 30832230›Full record

Trial reportNutrients2019

Oral Glutamine Supplementation Reduces Obesity, Pro-Inflammatory Markers, and Improves Insulin Sensitivity in DIO Wistar Rats and Reduces Waist Circumference in Overweight and Obese Humans.

Kahlile Youssef Abboud, Sabrina Karen Reis, Maria Eduarda Martelli, Olivia Pizetta Zordão, Fabiana Tannihão, Alessandra Zanin Zambom de Souza, Heloisa Balan Assalin, Dioze Guadagnini, Guilherme Zweig Rocha, Mario Jose Abdalla Saad and 1 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Glutamine metabolism in health and disease.Signal transduction and targeted therapy · 2026
    Review
  5. Article
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  9. Metabolomics: Uncovering Insights into Obesity and Diabetes.International journal of molecular sciences · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
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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

11 authors at 1 institution in 1 country.

Kahlile Youssef AbboudSchool of Applied Sciences, State University of Campinas (UNICAMP), Limeira 13484-350 SP, Brazil. kahlilebbd@gmail.com.ORCID 0000-0002-9132-7409
Sabrina Karen ReisSchool of Applied Sciences, State University of Campinas (UNICAMP), Limeira 13484-350 SP, Brazil. reis.sabrinakaren@gmail.com.ORCID 0000-0003-3967-0792
Maria Eduarda MartelliSchool of Applied Sciences, State University of Campinas (UNICAMP), Limeira 13484-350 SP, Brazil. mariaeduardamartelli@hotmail.com.
Olivia Pizetta ZordãoDepartment of Internal Medicine, State University of Campinas (UNICAMP), Campinas 13083-887 SP, Brazil. oliviapizetta@hotmail.com.ORCID 0000-0003-0596-1954
Fabiana TannihãoSchool of Applied Sciences, State University of Campinas (UNICAMP), Limeira 13484-350 SP, Brazil. ftannihao@yahoo.com.br.
Alessandra Zanin Zambom de SouzaSchool of Applied Sciences, State University of Campinas (UNICAMP), Limeira 13484-350 SP, Brazil. alessandrazz@hotmail.com.
Heloisa Balan AssalinDepartment of Internal Medicine, State University of Campinas (UNICAMP), Campinas 13083-887 SP, Brazil. helo_assalin@yahoo.com.br.
Dioze GuadagniniDepartment of Internal Medicine, State University of Campinas (UNICAMP), Campinas 13083-887 SP, Brazil. diozeg@gmail.com.
Guilherme Zweig RochaDepartment of Internal Medicine, State University of Campinas (UNICAMP), Campinas 13083-887 SP, Brazil. gzrocha@gmail.com.ORCID 0000-0002-7403-3230
Mario Jose Abdalla SaadDepartment of Internal Medicine, State University of Campinas (UNICAMP), Campinas 13083-887 SP, Brazil. msaad@fcm.unicamp.br.
Patricia Oliveira PradaSchool of Applied Sciences, State University of Campinas (UNICAMP), Limeira 13484-350 SP, Brazil. pprada.fca@gmail.com.
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/18498-6
6 · The paper itself

Abstract

In the present study, we aimed to investigate whether chronic oral glutamine (Gln) supplementation may alter metabolic parameters and the inflammatory profile in overweight and obese humans as well as whether Gln may modulate molecular pathways in key tissues linked to the insulin action in rats. Thirty-nine overweight/obese volunteers received 30 g of Gln or alanine (Ala-control) for 14 days. Body weight (BW), waist circumference (WC), hormones, and pro-inflammatory markers were evaluated. To investigate molecular mechanisms, Gln or Ala was given to Wistar rats on a high-fat diet (HFD), and metabolic parameters, euglycemic hyperinsulinemic clamp with tracers, and Western blot were done. Gln reduced WC and serum lipopolysaccharide (LPS) in overweight volunteers. In the obese group, Gln diminished WC and serum insulin. There was a positive correlation between the reduction on WC and LPS. In rats on HFD, Gln reduced adiposity, improved insulin action and signaling, and reversed both defects in glucose metabolism in the liver and muscle. Gln supplementation increased muscle glucose uptake and reversed the increased hepatic glucose production, in parallel with a reduced glucose uptake in adipose tissue. This insulin resistance in AT was accompanied by enhanced IRS1 O-linked-glycosamine association in this tissue, but not in the liver and muscle. These data suggest that Gln supplementation leads to insulin resistance specifically in adipose tissue via the hexosamine pathway and reduces adipose mass, which is associated with improvement in the systemic insulin action. Thus, further investigation with Gln supplementation should be performed for longer periods in humans before prescribing as a beneficial therapeutic approach for individuals who are overweight and obese.

Indexed as

Dietary SupplementsAdultAnimalsBiomarkersBody WeightDiet, High-FatDouble-Blind MethodFemaleGlucose Clamp TechniqueGlutamineHumansInflammation MediatorsInsulin ResistanceLiverMaleMuscle, SkeletalBiomarkersGlutamineInflammation Mediatorsclampcytokinesglutamine supplementationhexosamineinflammationinsulin sensitivityLPSobesity

Identifiers

PMID30832230
PMCPMC6471297
OpenAlexW2915111749

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.