Evidence map›Paper›PMID 26594198›Full record

ReviewFrontiers in endocrinology2015

Sexual Dimorphism of Adipose and Hepatic Aquaglyceroporins in Health and Metabolic Disorders.

Amaia Rodríguez, Raul A Marinelli, Angela Tesse, Gema Frühbeck, Giuseppe Calamita

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2015. 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
4.5field-weighted citation impact, top 5% 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, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. An Atherogenic Diet DisturbsBiomedicines · 2021
    Article
  14. Article
  15. Review
  16. Nuclear Receptor Regulation of Aquaglyceroporins in Metabolic Organs.International journal of molecular sciences · 2018
    Review
  17. Revisiting the metabolic syndrome: the emerging role of aquaglyceroporins.Cellular and molecular life sciences : CMLS · 2018
    Review
  18. Article
  19. Article
  20. Aquaporins as Targets of Dietary Bioactive Phytocompounds.Frontiers in molecular biosciences · 2018
    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

5 authors at 4 institutions in 3 countries.

Amaia RodríguezMetabolic Research Laboratory, CIBEROBN, IdiSNA, Clínica Universidad de Navarra , Pamplona , Spain.
Raul A MarinelliFacultad de Ciencias Bioquímicas y Farmacéuticas, Instituto de Fisiología Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional de Rosario , Rosario , Argentina.
Angela TesseINSERM UMR 1087/CNRS UMR 629, L'Institut du Thorax, IRS-UN , Nantes , France.
Gema FrühbeckMetabolic Research Laboratory, CIBEROBN, IdiSNA, Clínica Universidad de Navarra , Pamplona , Spain.
Giuseppe CalamitaDepartment of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari "Aldo Moro" , Bari , Italy.
Clinica Universidad de Navarra · ESInstitut du Thorax · FRInstituto de Fisiología Vegetal · ARSpanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gender differences in the relative risk of developing metabolic complications, such as insulin resistance or non-alcoholic fatty liver disease (NAFLD), have been reported. The deregulation of glycerol metabolism partly contributes to the onset of these metabolic diseases, since glycerol constitutes a key substrate for the synthesis of triacylglycerols (TAGs) as well as for hepatic gluconeogenesis. The present mini-review covers the sex--related differences in glycerol metabolism and aquaglyceroporins (AQPs) and its impact in the control of adipose and hepatic fat accumulation as well as in whole-body glucose homeostasis. Plasma glycerol concentrations are increased in women compared to men probably due to the higher lipolytic rate and larger AQP7 amounts in visceral fat as well as the well-known sexual dimorphism in fat mass with women showing higher adiposity. AQP9 represents the primary route for glycerol uptake in hepatocytes, where glycerol is converted by the glycerol-kinase enzyme into glycerol-3-phosphate, a key substrate for de novo synthesis of glucose and TAG. In spite of showing similar hepatic AQP9 protein, women exhibit lower hepatocyte glycerol permeability than men, which might contribute to their lower prevalence of insulin resistance and NAFLD.

Indexed as

aquaglyceroporinsfatty liver diseasegender dimorphismglycerolinsulin resistancemetabolismobesity

Identifiers

PMID26594198
PMCPMC4633488
OpenAlexW2168319071

What OpenQuestion holds

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LicenceCC BY
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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.