Evidence map›Paper›PMID 25027224›Full record

ArticleInternational journal of obesity (2005)2015

Transition from metabolic adaptation to maladaptation of the heart in obesity: role of apelin.

C Alfarano, C Foussal, O Lairez, D Calise, C Attané, R Anesia, D Daviaud, E Wanecq, A Parini, P Valet and 1 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in International journal of obesity (2005), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05202938 (Energy MEtabolism of Septic Heart.), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.6field-weighted citation impact, top 6% 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.

NCT05202938 unknown statusnot on this mapstarted 2022, after this paper: background citation

Energy MEtabolism of Septic Heart.

TypeobservationalSponsorCentre de recherche du Centre hospitalier universitaire de SherbrookeRan2022 to 2024Enrolled32ConditionsSeptic Shock, Chronic Heart FailureArmsultrasound cardiography, FDG PET scan, Palmitate PET scan, Acetate PET scan, Blood sampling
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 46 citations in OpenAlex.

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  19. Apelin and energy metabolism.Frontiers in physiology · 2015
    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

11 authors at 3 institutions in 1 country.

C Alfarano1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
C Foussal1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
O LairezNational Institute of Health and Medical Research (INSERM) U1048, Toulouse, France.
D Calise1] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France [2] US006, Microsurgery Services, Toulouse, France.
C Attané1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
R Anesia1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
D Daviaud1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
E Wanecq1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
A Parini1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
P Valet1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
O Kunduzova1] National Institute of Health and Medical Research (INSERM) U1048, Toulouse, France [2] University of Toulouse, UPS, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
Inserm · FRInstitut des Maladies Métaboliques et Cardiovasculaires · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesImpaired energy metabolism is the defining characteristic of obesity-related heart failure. The adipocyte-derived peptide apelin has a role in the regulation of cardiovascular and metabolic homeostasis and may contribute to the link between obesity, energy metabolism and cardiac function. Here we investigate the role of apelin in the transition from metabolic adaptation to maladaptation of the heart in obese state.

methodsAdult male C57BL/6J, apelin knock-out (KO) or wild-type mice were fed a high-fat diet (HFD) for 18 weeks. To induce heart failure, mice were subjected to pressure overload after 18 weeks of HFD. Long-term effects of apelin on fatty acid (FA) oxidation, glucose metabolism, cardiac function and mitochondrial changes were evaluated in HFD-fed mice after 4 weeks of pressure overload. Cardiomyocytes from HFD-fed mice were isolated for analysis of metabolic responses.

resultsIn HFD-fed mice, pressure overload-induced transition from hypertrophy to heart failure is associated with reduced FA utilization (P<0.05), accelerated glucose oxidation (P<0.05) and mitochondrial damage. Treatment of HFD-fed mice with apelin for 4 weeks prevented pressure overload-induced decline in FA metabolism (P<0.05) and mitochondrial defects. Furthermore, apelin treatment lowered fasting plasma glucose (P<0.01), improved glucose tolerance (P<0.05) and preserved cardiac function (P<0.05) in HFD-fed mice subjected to pressure overload. In apelin KO HFD-fed mice, spontaneous cardiac dysfunction is associated with reduced FA oxidation (P<0.001) and increased glucose oxidation (P<0.05). In isolated cardiomyocytes, apelin stimulated FA oxidation in a dose-dependent manner and this effect was prevented by small interfering RNA sirtuin 3 knockdown.

conclusionsThese data suggest that obesity-related decline in cardiac function is associated with defective myocardial energy metabolism and mitochondrial abnormalities. Furthermore, our work points for therapeutic potential of apelin to prevent myocardial metabolic abnormalities in heart failure paired with obesity.

Indexed as

AdipokinesAnimalsApelinDiet, High-FatDisease Models, AnimalHeart FailureIntercellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMyocardiumMyocytes, CardiacObesityOxidation-ReductionAdipokinesApelinApln protein, mouseIntercellular Signaling Peptides and Proteins

Identifiers

PMID25027224
PMCPMC4326962
OpenAlexW2030296258

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.