Evidence map›Paper›PMID 30460617›Full record

ArticleMolecular neurobiology2019

Differential Role of Hypothalamic AMPKα Isoforms in Fish: an Evolutive Perspective.

Marta Conde-Sieira, Valentina Capelli, Rosa Álvarez-Otero, Sara Comesaña, Laura Liñares-Pose, Cristina Velasco, Miguel López, José L Soengas

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
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

8 authors at 2 institutions in 1 country.

Marta Conde-SieiraLaboratorio de Fisioloxía Animal, Departamento de Bioloxía Funcional e Ciencias da Saúde, Facultade de Bioloxía and Centro de Investigación Mariña, Edificio de Ciencias Experimentais, Universidade de Vigo, 36310, Vigo, Spain.
Valentina CapelliDepartamento de Fisiología, Grupo NeurObesity, CIMUS, Universidade de Santiago de Compostela-Instituto de Investigación Sanitaria and CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), 15706, Santiago de Compostela, Spain.
Rosa Álvarez-OteroLaboratorio de Fisioloxía Animal, Departamento de Bioloxía Funcional e Ciencias da Saúde, Facultade de Bioloxía and Centro de Investigación Mariña, Edificio de Ciencias Experimentais, Universidade de Vigo, 36310, Vigo, Spain.
Sara ComesañaLaboratorio de Fisioloxía Animal, Departamento de Bioloxía Funcional e Ciencias da Saúde, Facultade de Bioloxía and Centro de Investigación Mariña, Edificio de Ciencias Experimentais, Universidade de Vigo, 36310, Vigo, Spain.
Laura Liñares-PoseDepartamento de Fisiología, Grupo NeurObesity, CIMUS, Universidade de Santiago de Compostela-Instituto de Investigación Sanitaria and CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), 15706, Santiago de Compostela, Spain.
Cristina VelascoLaboratorio de Fisioloxía Animal, Departamento de Bioloxía Funcional e Ciencias da Saúde, Facultade de Bioloxía and Centro de Investigación Mariña, Edificio de Ciencias Experimentais, Universidade de Vigo, 36310, Vigo, Spain.
Miguel LópezDepartamento de Fisiología, Grupo NeurObesity, CIMUS, Universidade de Santiago de Compostela-Instituto de Investigación Sanitaria and CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), 15706, Santiago de Compostela, Spain.
José L SoengasLaboratorio de Fisioloxía Animal, Departamento de Bioloxía Funcional e Ciencias da Saúde, Facultade de Bioloxía and Centro de Investigación Mariña, Edificio de Ciencias Experimentais, Universidade de Vigo, 36310, Vigo, Spain. jsoengas@uvigo.es.ORCID http://orcid.org/0000-0002-6847-3993
Universidade de Vigo · ESUniversidade de Santiago de Compostela · ES

Funding

Ministerio de Economía, Industria y Competitividad, Gobierno de España AGL2016-74857-C3-1-RMinisterio de Economía, Industria y Competitividad, Gobierno de España IJCI-2016-30499Ministerio de Economía, Industria y Competitividad, Gobierno de España SAF2015-71026-RMinisterio de Educación, Cultura y Deporte FPU16/00045
6 · The paper itself

Abstract

In mammals, hypothalamic AMP-activated protein kinase (AMPK) α1 and α2 isoforms mainly relate to regulation of thermogenesis/liver metabolism and food intake, respectively. Since both isoforms are present in fish, which do not thermoregulate, we assessed their role(s) in hypothalamus regarding control of food intake and energy homeostasis. Since many fish species are carnivorous and mostly mammals are omnivorous, assessing if the role of hypothalamic AMPK is different is also an open question. Using the rainbow trout as a fish model, we first observed that food deprivation for 5 days did not significantly increase phosphorylation status of AMPKα in hypothalamus. Then, we administered adenoviral vectors that express dominant negative (DN) AMPKα1 or AMPKα2 isoforms. The inhibition of AMPKα2 (but not AMPKα1) led to decreased food intake. The central inhibition of AMPKα2 resulted in liver with decreased capacity of use and synthesis of glucose, lipids, and amino acids suggesting that a signal of nutrient abundance flows from hypothalamus to the liver, thus suggesting a role for central AMPKα2 in the regulation of peripheral metabolism in fishes. The central inhibition of AMPKα1 induced comparable changes in liver metabolism though at a lower extent. From an evolutionary point of view, it is of interest that the function of central AMPKα2 remained similar throughout the vertebrate lineage. In contrast, the function of central AMPKα1 in fish relates to modulation of liver metabolism whereas in mammals modulates not only liver metabolism but also brown adipose tissue and thermogenesis.

Indexed as

Evolution, MolecularAMP-Activated Protein KinasesAnimalsHypothalamusIsoenzymesOncorhynchus mykissAMP-Activated Protein KinasesIsoenzymesAMPK isoformsFood intakeHepatic metabolismHypothalamusTrout

Identifiers

PMID30460617
OpenAlexW2901171777

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.