Evidence map›Paper›PMID 32738301›Full record

ArticleBiochimica et biophysica acta. Molecular and cell biology of lipids2020

Palmitoleic acid reduces high fat diet-induced liver inflammation by promoting PPAR-γ-independent M2a polarization of myeloid cells.

Camila O Souza, Alexandre A S Teixeira, Luana Amorim Biondo, Loreana Sanches Silveira, Cristiane N de Souza Breda, Tarcio T Braga, Niels O S Camara, Thiago Belchior, William T Festuccia, Tiego A Diniz and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular and cell biology of lipids, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.4field-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

30 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Palmitoleic acid loss links pulmonary dysbiosis to lung injury after single-lung ventilation.American journal of respiratory cell and molecular biology · 2026
    Article
  5. Article
  6. Article
  7. Article
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  9. Article
  10. Article
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  12. Article
  13. Review
  14. Article
  15. Adipose tissue-derived lipokines in metabolism.Current opinion in genetics & development · 2023
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

18 authors at 1 institution in 1 country.

Camila O SouzaDepartment of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Alexandre A S TeixeiraDepartment of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Luana Amorim BiondoDepartment of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Loreana Sanches SilveiraDepartment of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Cristiane N de Souza BredaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Tarcio T BragaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Niels O S CamaraDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Thiago BelchiorDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
William T FestucciaDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Tiego A DinizDepartment of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Glaucio Monteiro FerreiraLaboratory of Molecular Biology applied to Diagnosis (LBMAD), Department of Pharmacy, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Mario Hiroyuki HirataLaboratory of Molecular Biology applied to Diagnosis (LBMAD), Department of Pharmacy, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Adriano B Chaves-FilhoDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Marcos Y YoshinagaDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, SP, Brazil.
Sayuri MiyamotoDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, SP, Brazil.
Philip C CalderHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK; National Institute for Health Research Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton National Health Service (NHS) Foundation Trust, Southampton, UK; Institute for Life Sciences, University of Southampton, Southampton, UK.
Jaswinder K SethiHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK; National Institute for Health Research Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton National Health Service (NHS) Foundation Trust, Southampton, UK; Institute for Life Sciences, University of Southampton, Southampton, UK.
José C Rosa NetoDepartment of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil. Electronic address: josecesar23@hotmail.com.
Universidade de São Paulo · BR

Funding

Wellcome Trust 206453/Z/17/Z
6 · The paper itself

Abstract

Palmitoleic acid (POA, 16:1n-7) is a lipokine that has potential nutraceutical use to treat non-alcoholic fatty liver disease. We tested the effects of POA supplementation (daily oral gavage, 300 mg/Kg, 15 days) on murine liver inflammation induced by a high fat diet (HFD, 59% fat, 12 weeks). In HFD-fed mice, POA supplementation reduced serum insulin and improved insulin tolerance compared with oleic acid (OA, 300 mg/Kg). The livers of POA-treated mice exhibited less steatosis and inflammation than those of OA-treated mice with lower inflammatory cytokine levels and reduced toll-like receptor 4 protein content. The anti-inflammatory effects of POA in the liver were accompanied by a reduction in liver macrophages (LM, CD11c

Indexed as

AMP-Activated Protein Kinase KinasesAnimalsB7-2 AntigenCD11c AntigenDiet, High-FatFatty Acids, MonounsaturatedHumansInflammationInsulin ResistanceLectins, C-TypeLiverMannose-Binding LectinsMannose ReceptorMiceMyeloid CellsNon-alcoholic Fatty Liver DiseaseAMP-Activated Protein Kinase KinasesB7-2 AntigenCD11c AntigenFatty Acids, MonounsaturatedLectins, C-TypeMannose-Binding LectinsMannose ReceptorOleic Acidpalmitoleic acidPPAR gammaPparg protein, mouseProtein KinasesReceptors, Cell SurfaceHepatic macrophagesInflammationNon-alcoholic fatty liver diseaseObesityPalmitoleic acid

Identifiers

PMID32738301
PMCPMC7487782
OpenAlexW3046149665

What OpenQuestion holds

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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.