Evidence map›Paper›PMID 25856396›Full record

ArticlePloS one2015

Opposing activity changes in AMP deaminase and AMP-activated protein kinase in the hibernating ground squirrel.

Miguel A Lanaspa, L Elaine Epperson, Nanxing Li, Christina Cicerchi, Gabriela E Garcia, Carlos A Roncal-Jimenez, Jessica Trostel, Swati Jain, Colin T Mant, Christopher J Rivard and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  6. The fructose survival hypothesis for obesity.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
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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 5 institutions in 3 countries.

Miguel A LanaspaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
L Elaine EppersonDepartment of Cell and Developmental Biology, Aurora, CO, 80045, United States of America.
Nanxing LiDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Christina CicerchiDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Gabriela E GarciaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Carlos A Roncal-JimenezDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Jessica TrostelDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Swati JainDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Colin T MantDepartment of Biochemistry and Molecular Genetics, Aurora, CO, 80045, United States of America.
Christopher J RivardDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Takuji IshimotoDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Michiko ShimadaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Laura Gabriela Sanchez-LozadaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America; Laboratory of Renal Physiopathology and Nephrology Dept, INC Ignacio Chavez, Mexico City, Mexico.
Takahiko NakagawaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Alkesh JaniDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America.
Peter StenvinkelDivision of Renal Medicine, Department of Clinical Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Sandra L MartinDepartment of Cell and Developmental Biology, Aurora, CO, 80045, United States of America.
Richard J JohnsonDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, 80045, United States of America; Division of Nephrology, Eastern Colorado Health System, Department of Veteran Affairs, Denver, CO, United States of America.
University of Colorado Denver · USThe Medical Center of Aurora · USInstituto Nacional de Cardiología · MXKarolinska Institutet · SEVA Eastern Colorado Health Care System · US

Funding

Role of Uric Acid in Hypertension and Renal DiseaseR01HL068607 · NHLBI · UNIVERSITY OF FLORIDA · PI JOHNSON, RICHARD JOSEPH · 2002 to 2011
$3.5M
Development of inhibitors of AMP Deaminase Isoform 2 as a Mechanism for TreatingRC4DK090859 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JOHNSON, RICHARD JOSEPH · 2010 to 2010
$2.3M
Biomarkers for the two phase switches of mammalian hibernationR01HL089049 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MARTIN, SANDRA L · 2008 to 2011
$1.5M
Reduction of kidney progressive fibrosis by A2A adenosine receptor activation: PR01DK082509 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI GARCIA, GABRIELA E · 2011 to 2015
$1.3M
NHLBI NIH HHS HL089049NHLBI NIH HHS HL68607NHLBI NIH HHS R01 HL068607NHLBI NIH HHS R01 HL089049NIDDK NIH HHS R01 DK082509NIDDK NIH HHS RC4 DK090859NIDDK NIH HHS RC4 DK90859
6 · The paper itself

Abstract

Hibernating animals develop fatty liver when active in summertime and undergo a switch to a fat oxidation state in the winter. We hypothesized that this switch might be determined by AMP and the dominance of opposing effects: metabolism through AMP deaminase (AMPD2) (summer) and activation of AMP-activated protein kinase (AMPK) (winter). Liver samples were obtained from 13-lined ground squirrels at different times during the year, including summer and multiples stages of winter hibernation, and fat synthesis and β-fatty acid oxidation were evaluated. Changes in fat metabolism were correlated with changes in AMPD2 activity and intrahepatic uric acid (downstream product of AMPD2), as well as changes in AMPK and intrahepatic β-hydroxybutyrate (a marker of fat oxidation). Hepatic fat accumulation occurred during the summer with relatively increased enzymes associated with fat synthesis (FAS, ACL and ACC) and decreased enoyl CoA hydratase (ECH1) and carnitine palmitoyltransferase 1A (CPT1A), rate limiting enzymes of fat oxidation. In summer, AMPD2 activity and intrahepatic uric acid levels were high and hepatic AMPK activity was low. In contrast, the active phosphorylated form of AMPK and β-hydroxybutyrate both increased during winter hibernation. Therefore, changes in AMPD2 and AMPK activity were paralleled with changes in fat synthesis and fat oxidation rates during the summer-winter cycle. These data illuminate the opposing forces of metabolism of AMP by AMPD2 and its availability to activate AMPK as a switch that governs fat metabolism in the liver of hibernating ground squirrel.

Indexed as

Adipose TissueAMP-Activated Protein KinasesAMP DeaminaseAnimalsFatty AcidsGlucoseHibernationLipid MetabolismLiverOxidation-ReductionSciuridaeSeasonsAMP-Activated Protein KinasesAMP DeaminaseFatty AcidsGlucose

Identifiers

PMID25856396
PMCPMC4391924
OpenAlexW2092061890

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.