Articles producció científica> Medicina i Cirurgia

Protective effects of the succinate/SUCNR1 axis on damaged hepatocytes in NAFLD

  • Datos identificativos

    Identificador: imarina:9321837
    Autores:
    Marsal-Beltran, ARodríguez-Castellano, AAstiarraga, BCalvo, ERada, PMadeira, ARodríguez-Peña, MMLlauradó, GNúñez-Roa, CGómez-Santos, BMaymó-Masip, EBosch, RFrutos, MDMoreno-Navarrete, JMRamos-Molina, BAspichueta, PJoven, JFernández-Real, JMQuera, JCValverde, AMPardo, AVendrell, JCeperuelo-Mallafré, VFernández-Veledo, S
    Resumen:
    Succinate and succinate receptor 1 (SUCNR1) are linked to fibrotic remodeling in models of non-alcoholic fatty liver disease (NAFLD), but whether they have roles beyond the activation of hepatic stellate cells remains unexplored. We investigated the succinate/SUCNR1 axis in the context of NAFLD specifically in hepatocytes.We studied the phenotype of wild-type and Sucnr1-/- mice fed a choline-deficient high-fat diet to induce non-alcoholic steatohepatitis (NASH), and explored the function of SUCNR1 in murine primary hepatocytes and human HepG2 cells treated with palmitic acid. Lastly, plasma succinate and hepatic SUCNR1 expression were analyzed in four independent cohorts of patients in different NAFLD stages.Sucnr1 was upregulated in murine liver and primary hepatocytes in response to diet-induced NASH. Sucnr1 deficiency provoked both beneficial (reduced fibrosis and endoplasmic reticulum stress) and detrimental (exacerbated steatosis and inflammation and reduced glycogen content) effects in the liver, and disrupted glucose homeostasis. Studies in vitro revealed that hepatocyte injury increased Sucnr1 expression, which when activated improved lipid and glycogen homeostasis in damaged hepatocytes. In humans, SUCNR1 expression was a good determinant of NAFLD progression to advanced stages. In a population at risk of NAFLD, circulating succinate was elevated in patients with a fatty liver index (FLI) ≥60. Indeed, succinate had good predictive value for steatosis diagnosed by FLI, and improved the prediction of moderate/severe steatosis through biopsy when added to an FLI algorithm.We identify hepatocytes as target cells of extracellular succinate during NAFLD progression and uncover a hitherto unknown function for SUCNR1 as a regulator of hepatocyte glucose and lipid metab
  • Otros:

    Autor según el artículo: Marsal-Beltran, A; Rodríguez-Castellano, A; Astiarraga, B; Calvo, E; Rada, P; Madeira, A; Rodríguez-Peña, MM; Llauradó, G; Núñez-Roa, C; Gómez-Santos, B; Maymó-Masip, E; Bosch, R; Frutos, MD; Moreno-Navarrete, JM; Ramos-Molina, B; Aspichueta, P; Joven, J; Fernández-Real, JM; Quera, JC; Valverde, AM; Pardo, A; Vendrell, J; Ceperuelo-Mallafré, V; Fernández-Veledo, S
    Departamento: Medicina i Cirurgia Bioquímica i Biotecnologia
    Autor/es de la URV: Bosch Príncep, Ramon / Calvo Manso, Enrique / Ceperuelo Mallafré, Maria Victoria / Domínguez Porfirio, Brenno / Fernandez Veledo, Sonia / Joven Maried, Jorge / MARSAL BELTRAN, ANNA / Maymo Masip, Elsa / Pardo Balteiro, Alberto / Quer Boniquet, Juan Carlos / Rodríguez Castellano, Adrià / RODRIGUEZ PEÑA, MARIA DEL MAR / Vendrell Ortega, Juan
    Palabras clave: Sucnr1 Succinate Steatosis Nash Hepatocyte Hepatic stellate cells Glycogen sucnr1 steatosis receptor nash metabolism hepatocyte gpr91 glycogen fibrosis expression antagonist activation
    Resumen: Succinate and succinate receptor 1 (SUCNR1) are linked to fibrotic remodeling in models of non-alcoholic fatty liver disease (NAFLD), but whether they have roles beyond the activation of hepatic stellate cells remains unexplored. We investigated the succinate/SUCNR1 axis in the context of NAFLD specifically in hepatocytes.We studied the phenotype of wild-type and Sucnr1-/- mice fed a choline-deficient high-fat diet to induce non-alcoholic steatohepatitis (NASH), and explored the function of SUCNR1 in murine primary hepatocytes and human HepG2 cells treated with palmitic acid. Lastly, plasma succinate and hepatic SUCNR1 expression were analyzed in four independent cohorts of patients in different NAFLD stages.Sucnr1 was upregulated in murine liver and primary hepatocytes in response to diet-induced NASH. Sucnr1 deficiency provoked both beneficial (reduced fibrosis and endoplasmic reticulum stress) and detrimental (exacerbated steatosis and inflammation and reduced glycogen content) effects in the liver, and disrupted glucose homeostasis. Studies in vitro revealed that hepatocyte injury increased Sucnr1 expression, which when activated improved lipid and glycogen homeostasis in damaged hepatocytes. In humans, SUCNR1 expression was a good determinant of NAFLD progression to advanced stages. In a population at risk of NAFLD, circulating succinate was elevated in patients with a fatty liver index (FLI) ≥60. Indeed, succinate had good predictive value for steatosis diagnosed by FLI, and improved the prediction of moderate/severe steatosis through biopsy when added to an FLI algorithm.We identify hepatocytes as target cells of extracellular succinate during NAFLD progression and uncover a hitherto unknown function for SUCNR1 as a regulator of hepatocyte glucose and lipid metabolism. Our clinical data highlight the potential of succinate and hepatic SUCNR1 expression as markers to diagnose fatty liver and NASH, respectively.Copyright © 2023. Published by Elsevier Inc.
    Áreas temáticas: 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
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    Direcció de correo del autor: anna.marsal@urv.cat brenno.dominguez@urv.cat sonia.fernandez@urv.cat alberto.pardo@urv.cat ramon.bosch@urv.cat elsa.maymo@urv.cat juancarlos.quer@urv.cat enrique.calvo@urv.cat victoria.ceperuelo@urv.cat anna.marsal@urv.cat ramon.bosch@urv.cat adria.rodriguez@estudiants.urv.cat jorge.joven@urv.cat juanjose.vendrell@urv.cat
    Identificador del autor: 0000-0003-2216-8974 0000-0003-2906-3788 0000-0002-9133-3120 0000-0002-4460-9761 0000-0003-2749-4541 0000-0002-6994-6115
    Fecha de alta del registro: 2024-08-03
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Enlace a la fuente original: https://www.metabolismjournal.com/article/S0026-0495(23)00234-2/fulltext
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Metabolism-Clinical And Experimental. 145 155630-155630
    Referencia de l'ítem segons les normes APA: Marsal-Beltran, A; Rodríguez-Castellano, A; Astiarraga, B; Calvo, E; Rada, P; Madeira, A; Rodríguez-Peña, MM; Llauradó, G; Núñez-Roa, C; Gómez-Santos, (2023). Protective effects of the succinate/SUCNR1 axis on damaged hepatocytes in NAFLD. Metabolism-Clinical And Experimental, 145(), 155630-155630. DOI: 10.1016/j.metabol.2023.155630
    DOI del artículo: 10.1016/j.metabol.2023.155630
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2023
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Endocrinology,Endocrinology & Metabolism,Endocrinology, Diabetes and Metabolism
    Sucnr1
    Succinate
    Steatosis
    Nash
    Hepatocyte
    Hepatic stellate cells
    Glycogen
    sucnr1
    steatosis
    receptor
    nash
    metabolism
    hepatocyte
    gpr91
    glycogen
    fibrosis
    expression
    antagonist
    activation
    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
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