Evidence map›Paper›PMID 28895586›Full record

ArticleInternational journal of obesity (2005)2018

Maresin 1 mitigates liver steatosis in ob/ob and diet-induced obese mice.

L M Laiglesia, S Lorente-Cebrián, L Martínez-Fernández, N Sáinz, P L Prieto-Hontoria, M A Burrell, C M Rodríguez-Ortigosa, J A Martínez, M J Moreno-Aliaga

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 3 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

45 citing papers in PubMed, 3 syntheses or guidelines pooled it, 165 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Maresins.Biomolecules · 2026
    Review
  7. Article
  8. Review
  9. Brown Adipose Tissue Activation in Humans Increases Plasma Levels of Lipid Mediators.The Journal of clinical endocrinology and metabolism · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Maresin-1 and Inflammatory Disease.International journal of molecular sciences · 2022
    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

9 authors at 4 institutions in 1 country.

L M LaiglesiaUniversity of Navarra, Department of Nutrition, Food Science and Physiology, Pamplona, Spain.
S Lorente-CebriánUniversity of Navarra, Department of Nutrition, Food Science and Physiology, Pamplona, Spain.
L Martínez-FernándezUniversity of Navarra, Department of Nutrition, Food Science and Physiology, Pamplona, Spain.
N SáinzUniversity of Navarra, Centre for Nutrition Research, Pamplona, Spain.
P L Prieto-HontoriaUniversity of Navarra, Department of Nutrition, Food Science and Physiology, Pamplona, Spain.
M A BurrellUniversity of Navarra, Department of Histology and Pathology, Pamplona, Spain.
C M Rodríguez-OrtigosaHepatology Program, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
J A MartínezUniversity of Navarra, Department of Nutrition, Food Science and Physiology, Pamplona, Spain.
M J Moreno-AliagaUniversity of Navarra, Department of Nutrition, Food Science and Physiology, Pamplona, Spain.
Universidad de Navarra · ESInstituto de Salud Carlos III · ESNavarre Institute of Health Research · ESSpanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesThe aim of this study was to characterize the effects of Maresin 1 (MaR1) in obesity-related liver steatosis and the mechanisms involved.

methodsMaR1 effects on fatty liver disease were tested in ob/ob (2-10 μg kg

resultsIn ob/ob mice, MaR1 reduced liver triglycerides (TG) content, fatty acid synthase (FAS) and stearoyl-CoA desaturase-1 protein expression, while increased acetyl-CoA carboxylase (ACC) phosphorylation and LC3II protein expression, in parallel with a drop in p62 levels. Similar effects on hepatic TG, ACC phosphorylation, p62 and LC3II were observed in DIO mice after MaR1 i.p. injection. Interestingly, oral gavage of MaR1 also decreased serum transaminases, reduced liver weight and TG content. MaR1-treated mice exhibited reduced hepatic lipogenic enzymes content (FAS) or activation (by phosphorylation of ACC), accompanied by upregulation of carnitine palmitoyltransferase (Cpt1a), acyl-coenzyme A oxidase (Acox1) and autophagy-related proteins 5 and 7 (Atg5-7) gene expression, along with increased number of autophagic vacuoles and reduced p62 protein levels. MaR1 also induced AMP-activated protein kinase (AMPK) phosphorylation in DIO mice and in primary hepatocytes, and AMPK inhibition completely blocked MaR1 effects on Cpt1a, Acox1, Atg5 and Atg7 expression.

conclusionsMaR1 ameliorates liver steatosis by decreasing lipogenic enzymes, while inducing fatty acid oxidation genes and autophagy, which could be related to AMPK activation. Thus, MaR1 may be a new therapeutic candidate for reducing fatty liver in obesity.

Indexed as

LiverAnimalsBody WeightCells, CulturedDiet, High-FatDocosahexaenoic AcidsFatty LiverHepatocytesLipid MetabolismMaleMiceMice, Inbred C57BLMice, ObeseObesity7,14-dihydroxydocosa-4,8,10,12,16,19-hexaenoic acidDocosahexaenoic Acids

Identifiers

PMID28895586
OpenAlexW2756340976

What OpenQuestion holds

Textmetadata
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.