Evidence map›Paper›PMID 22179809›Full record

ArticleDiabetes2012

The L-α-lysophosphatidylinositol/GPR55 system and its potential role in human obesity.

José María Moreno-Navarrete, Victoria Catalán, Lauren Whyte, Adenis Díaz-Arteaga, Rafael Vázquez-Martínez, Fernando Rotellar, Rocío Guzmán, Javier Gómez-Ambrosi, Marina R Pulido, Wendy R Russell and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
8.7field-weighted citation impact, top 2% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 156 citations in OpenAlex.

  1. The Role of Cannabidiol in Liver Disease: A Systemic Review.International journal of molecular sciences · 2024
    Pooled it
  2. Article
  3. Astrocytic GPR55 receptors promote glycolysis.Journal of cannabis research · 2026
    Article
  4. Targeting the LPI/GPR55 Axis in MAFLD and MASH: Novel Insights, Therapeutic Strategies and Future Directions.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  5. Article
  6. Biology · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Cannabis Pharmacogenomics: A Path to Personalized Medicine.Current issues in molecular biology · 2023
    Review
  18. Review
  19. Article
  20. Article

16 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

17 authors at 7 institutions in 2 countries.

José María Moreno-NavarreteDepartment of Diabetes, Endocrinology, and Nutrition, Institut d’Investigació Biomédica de Girona Catalonia, Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y Nutrición, Girona, Spain.
Victoria Catalán
Lauren Whyte
Adenis Díaz-Arteaga
Rafael Vázquez-Martínez
Fernando Rotellar
Rocío Guzmán
Javier Gómez-Ambrosi
Marina R Pulido
Wendy R Russell
Mónica Imbernón
Ruth A Ross
María M Malagón
Carlos Dieguez
José Manuel Fernández-Real
Gema Frühbeck
Ruben Nogueiras
Centro de Investigación Biomédica en Red · ESUniversity of Aberdeen · GBClinica Universidad de Navarra · ESInstitut d'Investigació Biomèdica de Girona · ESUniversidad de Navarra · ESInstituto de Investigación Sanitaria de Santiago · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GPR55 is a putative cannabinoid receptor, and l-α-lysophosphatidylinositol (LPI) is its only known endogenous ligand. We investigated 1) whether GPR55 is expressed in fat and liver; 2) the correlation of both GPR55 and LPI with several metabolic parameters; and 3) the actions of LPI on human adipocytes. We analyzed CB1, CB2, and GPR55 gene expression and circulating LPI levels in two independent cohorts of obese and lean subjects, with both normal or impaired glucose tolerance and type 2 diabetes. Ex vivo experiments were used to measure intracellular calcium and lipid accumulation. GPR55 levels were augmented in the adipose tissue of obese subjects and further so in obese patients with type 2 diabetes when compared with nonobese subjects. Visceral adipose tissue GPR55 correlated positively with weight, BMI, and percent fat mass, particularly in women. Hepatic GPR55 gene expression was similar in obese and type 2 diabetic subjects. Circulating LPI levels were increased in obese patients and correlated with fat percentage and BMI in women. LPI increased the expression of lipogenic genes in visceral adipose tissue explants and intracellular calcium in differentiated visceral adipocytes. These findings indicate that the LPI/GPR55 system is positively associated with obesity in humans.

Indexed as

3T3-L1 CellsAdipocytesAdultAnimalsBody Mass IndexCalciumCell DifferentiationFemaleHumansIntra-Abdominal FatLinear ModelsLiverLysophospholipidsMaleMiceObesityCalciumGPR55 protein, humanlysophosphatidylinositolLysophospholipidsReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Receptors, CannabinoidReceptors, G-Protein-CoupledRNA, Messenger

Identifiers

PMID22179809
PMCPMC3266411
OpenAlexW2115824704

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.