Articles producció científica> Medicina i Cirurgia

Fatty acid binding protein 4 (FABP4) as a potential biomarker reflecting myocardial lipid storage in type 2 diabetes

  • Identification data

    Identifier: imarina:5097897
    Authors:
    Rodriguez-Calvo, RicardoGirona, JosefaRodriguez, MarinaSamino, SaraBarroso, Emmade Gonzalo-Calvo, DavidGuaita-Esteruelas, SandraHeras, Mercedesvan der Meer, Rutger WLamb, Hildo JYanes, OscarCorreig, XavierLlorente-Cortes, VicentaVazquez-Carrera, ManuelMasana, Lluis
    Abstract:
    © 2019 Elsevier Inc. Objective: Fatty acid binding protein 4 (FABP4) is an intracellular lipid chaperone involved in the crosstalk between adipose and peripheral tissues, and it contributes to widespread insulin resistance in cells, including cardiac cells. However, the role of this adipokine in regulating cardiac metabolism and myocardial neutral lipid content in patients with type 2 diabetes has not been elucidated. Methods: The impact of circulating FABP4 on the cardiac neutral lipid content was measured by proton magnetic resonance spectroscopy ( 1 H-MRS) in patients with type 2 diabetes. Additionally, circulating FABP4 and the cardiac triglyceride content were analysed in high-fat diet (HFD)-fed mice, and the impact of the exogenous FABP4 was explored in HL-1 cardiac cells. Results: Serum FABP4 levels were higher in type 2 diabetic patients compared to healthy individuals. Circulating FABP4 levels were associated with myocardial neutral lipid content in type 2 diabetic patients. In HFD-fed mice, both serum FABP4 and myocardial triglyceride content were increased. In FABP4-challenged HL-1 cells, extracellular FABP4 increased intracellular lipid accumulation, which led to impairment of the insulin-signalling pathway and reduced insulin-stimulated glucose uptake. However, these effects were partially reversed by FABP4 inhibition with BMS309403, which attenuated the intracellular lipid content and improved insulin signalling and insulin-stimulated glucose uptake. Conclusions: Taken together, our results identify FABP4 as a molecule involved in diabetic/lipid-induced cardiomyopathy and indicate that this molecule may be an emerging biomarker for diabetic cardiomyopathy-related disturbances, such as myocardial neutral lipid accumulation. Additionally, FABP4 inhibition m
  • Others:

    Author, as appears in the article.: Rodriguez-Calvo, Ricardo; Girona, Josefa; Rodriguez, Marina; Samino, Sara; Barroso, Emma; de Gonzalo-Calvo, David; Guaita-Esteruelas, Sandra; Heras, Mercedes; van der Meer, Rutger W; Lamb, Hildo J; Yanes, Oscar; Correig, Xavier; Llorente-Cortes, Vicenta; Vazquez-Carrera, Manuel; Masana, Lluis
    Department: Medicina i Cirurgia Ciències Mèdiques Bàsiques
    URV's Author/s: Correig Blanchar, Francesc Xavier / Girona Tell, Josefa / GUAITA ESTERUELAS, SANDRA / HERAS IBAÑEZ, MERCEDES / Masana Marín, Luis / Rodríguez Calvo, Ricardo / Rodríguez Chacón, Matilde / SAMINO GENÉ, SARA / Yanes Torrado, Óscar
    Keywords: Waist circumference Upregulation Unclassified drug Triglycerides Triglyceride content Triacylglycerol blood level Triacylglycerol Suppressor of cytokine signaling 3 Subcutaneous fat Steatosis Stat3 protein Signal transduction Resistin Pyruvate dehydrogenase kinase 4 Pyrazoles Pyrazole derivative Proton nuclear magnetic resonance Protein phosphorylation Protein inhibitor Protein expression level Protein blood level Phospholipid Non insulin dependent diabetes mellitus Myocardium Myocardial neutral lipid content Middle aged Mice, inbred c57bl Mice Metabolism Metabolic syndrome Messenger rna Male Low density lipoprotein cholesterol Lipid metabolism Leptin Left-ventricular mass Insulin-resistance Insulin resistance Insulin Humans High density lipoprotein cholesterol Hemoglobin a1c Heart-failure Glucose transporter 4 Glucose Female Fatty acid-binding proteins Fatty acid binding protein 4 Fatty acid binding protein Fatty acid Fabp4 protein, mouse Fabp4 protein, human Fabp4 Diet, high-fat Diabetic patient Diabetic cardiomyopathy Diabetic cardiomyopathies Diabetes mellitus, type 2 Coronary-artery-disease Controlled study Colecalciferol Cholesterol derivative Cell line Cardiac-function Cardiac muscle cell Cardiac muscle Cardiac lipotoxicity C57bl mouse Bms309403 Bms 309403 Blood biochemistry Blood Biphenyl derivative Biphenyl compounds Biomarkers Biological marker Article Animals Animal model Animal experiment Animal cell Animal Adipose-tissue Adiponectin Accumulation 2-(2'-(5-ethyl-3,4-diphenyl-1h-pyrazol-1-yl)biphenyl-3-yloxy)acetic acid insulin resistance fabp4 cardiac lipotoxicity bms309403
    Abstract: © 2019 Elsevier Inc. Objective: Fatty acid binding protein 4 (FABP4) is an intracellular lipid chaperone involved in the crosstalk between adipose and peripheral tissues, and it contributes to widespread insulin resistance in cells, including cardiac cells. However, the role of this adipokine in regulating cardiac metabolism and myocardial neutral lipid content in patients with type 2 diabetes has not been elucidated. Methods: The impact of circulating FABP4 on the cardiac neutral lipid content was measured by proton magnetic resonance spectroscopy ( 1 H-MRS) in patients with type 2 diabetes. Additionally, circulating FABP4 and the cardiac triglyceride content were analysed in high-fat diet (HFD)-fed mice, and the impact of the exogenous FABP4 was explored in HL-1 cardiac cells. Results: Serum FABP4 levels were higher in type 2 diabetic patients compared to healthy individuals. Circulating FABP4 levels were associated with myocardial neutral lipid content in type 2 diabetic patients. In HFD-fed mice, both serum FABP4 and myocardial triglyceride content were increased. In FABP4-challenged HL-1 cells, extracellular FABP4 increased intracellular lipid accumulation, which led to impairment of the insulin-signalling pathway and reduced insulin-stimulated glucose uptake. However, these effects were partially reversed by FABP4 inhibition with BMS309403, which attenuated the intracellular lipid content and improved insulin signalling and insulin-stimulated glucose uptake. Conclusions: Taken together, our results identify FABP4 as a molecule involved in diabetic/lipid-induced cardiomyopathy and indicate that this molecule may be an emerging biomarker for diabetic cardiomyopathy-related disturbances, such as myocardial neutral lipid accumulation. Additionally, FABP4 inhibition may be a potential therapeutic target for metabolic-related cardiac dysfunctions.
    Thematic Areas: Saúde coletiva Odontología Nutrição Medicina iii Medicina ii Medicina i Interdisciplinar General medicine Farmacia Engenharias ii Enfermagem Endocrinology, diabetes and metabolism Endocrinology & metabolism Endocrinology Educação física Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciência de alimentos Biotecnología Antropologia / arqueologia
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 00260495
    Author's mail: josefa.girona@urv.cat ricardo.rodriguez@urv.cat oscar.yanes@urv.cat matilde.rodriguez@urv.cat josefa.girona@urv.cat xavier.correig@urv.cat luis.masana@urv.cat
    Author identifier: 0000-0002-6267-8779 0000-0003-3695-7157 0000-0002-6267-8779 0000-0002-6902-3054 0000-0002-0789-4954
    Record's date: 2024-10-12
    Papper version: info:eu-repo/semantics/acceptedVersion
    Link to the original source: https://www.metabolismjournal.com/article/S0026-0495(19)30073-3/abstract
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Papper original source: Metabolism-Clinical And Experimental. 96 12-21
    APA: Rodriguez-Calvo, Ricardo; Girona, Josefa; Rodriguez, Marina; Samino, Sara; Barroso, Emma; de Gonzalo-Calvo, David; Guaita-Esteruelas, Sandra; Heras, M (2019). Fatty acid binding protein 4 (FABP4) as a potential biomarker reflecting myocardial lipid storage in type 2 diabetes. Metabolism-Clinical And Experimental, 96(), 12-21. DOI: 10.1016/j.metabol.2019.04.007
    Article's DOI: 10.1016/j.metabol.2019.04.007
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2019
    Publication Type: Journal Publications
  • Keywords:

    Endocrinology,Endocrinology & Metabolism,Endocrinology, Diabetes and Metabolism
    Waist circumference
    Upregulation
    Unclassified drug
    Triglycerides
    Triglyceride content
    Triacylglycerol blood level
    Triacylglycerol
    Suppressor of cytokine signaling 3
    Subcutaneous fat
    Steatosis
    Stat3 protein
    Signal transduction
    Resistin
    Pyruvate dehydrogenase kinase 4
    Pyrazoles
    Pyrazole derivative
    Proton nuclear magnetic resonance
    Protein phosphorylation
    Protein inhibitor
    Protein expression level
    Protein blood level
    Phospholipid
    Non insulin dependent diabetes mellitus
    Myocardium
    Myocardial neutral lipid content
    Middle aged
    Mice, inbred c57bl
    Mice
    Metabolism
    Metabolic syndrome
    Messenger rna
    Male
    Low density lipoprotein cholesterol
    Lipid metabolism
    Leptin
    Left-ventricular mass
    Insulin-resistance
    Insulin resistance
    Insulin
    Humans
    High density lipoprotein cholesterol
    Hemoglobin a1c
    Heart-failure
    Glucose transporter 4
    Glucose
    Female
    Fatty acid-binding proteins
    Fatty acid binding protein 4
    Fatty acid binding protein
    Fatty acid
    Fabp4 protein, mouse
    Fabp4 protein, human
    Fabp4
    Diet, high-fat
    Diabetic patient
    Diabetic cardiomyopathy
    Diabetic cardiomyopathies
    Diabetes mellitus, type 2
    Coronary-artery-disease
    Controlled study
    Colecalciferol
    Cholesterol derivative
    Cell line
    Cardiac-function
    Cardiac muscle cell
    Cardiac muscle
    Cardiac lipotoxicity
    C57bl mouse
    Bms309403
    Bms 309403
    Blood biochemistry
    Blood
    Biphenyl derivative
    Biphenyl compounds
    Biomarkers
    Biological marker
    Article
    Animals
    Animal model
    Animal experiment
    Animal cell
    Animal
    Adipose-tissue
    Adiponectin
    Accumulation
    2-(2'-(5-ethyl-3,4-diphenyl-1h-pyrazol-1-yl)biphenyl-3-yloxy)acetic acid
    insulin resistance
    fabp4
    cardiac lipotoxicity
    bms309403
    Saúde coletiva
    Odontología
    Nutrição
    Medicina iii
    Medicina ii
    Medicina i
    Interdisciplinar
    General medicine
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