Articles producció científicaBioquímica i Biotecnologia

Multi-tissue pro fi ling of oxylipins reveal a conserved up-regulation of epoxide:diol ratio that associates with white adipose tissue in fl ammation and liver steatosis in obesity

  • Dades identificatives

    Identificador:  imarina:9369674
    Autors:  Hateley, Charlotte; Olona, Antoni; Halliday, Laura; Edin, Matthew L; Ko, Jeong-Hun; Forlano, Roberta; Terra, Ximena; Lih, Fred B; Beltran-Debon, Raul; Manousou, Penelopi; Purkayastha, Sanjay; Moorthy, Krishna; Thursz, Mark R; Zhang, Guodong; Goldin, Robert D; Zeldin, Darryl C; Petretto, Enrico; Behmoaras, Jacques
    Resum:
    Background Obesity drives maladaptive changes in the white adipose tissue (WAT) which can progressively cause insulin resistance, type 2 diabetes mellitus (T2DM) and metabolic dysfunction -associated liver disease (MASLD). Obesity -mediated loss of WAT homeostasis can trigger liver steatosis through dysregulated lipid pathways such as those related to polyunsaturated fatty acid (PUFA)-derived oxylipins. However, the exact relationship between oxylipins and metabolic syndrome remains elusive and cross -tissue dynamics of oxylipins are ill-de fi ned. Methods We quanti fi ed PUFA-related oxylipin species in the omental WAT, liver biopsies and plasma of 88 patients undergoing bariatric surgery (female N = 79) and 9 patients (female N = 4) undergoing upper gastrointestinal surgery, using UPLC-MS/MS. We integrated oxylipin abundance with WAT phenotypes (adipogenesis, adipocyte hypertrophy, macrophage in fi ltration, type I and VI collagen remodelling) and the severity of MASLD (steatosis, in fl ammation, fi brosis) quanti fi ed in each biopsy. The integrative analysis was subjected to (i) adjustment for known risk factors and, (ii) control for potential drug -effects through UPLC-MS/MS analysis of metformin-treated fat explants ex vivo . Findings We reveal a generalized down -regulation of cytochrome P450 (CYP)-derived diols during obesity conserved between the WAT and plasma. Notably, epoxide:diol ratio, indicative of soluble epoxide hydrolyse (sEH) activity, increases with WAT in fl ammation/ fi brosis, hepatic steatosis and T2DM. Increased 12,13-EpOME:DiHOME in WAT and liver is a marker of worsening metabolic syndrome in patients with obesity. Interpretation These fi ndings suggest a dampened sEH activity and a possible role of fatty acid diols during metabolic syndrome in
  • Altres:

    Autor segons l'article: Hateley, Charlotte; Olona, Antoni; Halliday, Laura; Edin, Matthew L; Ko, Jeong-Hun; Forlano, Roberta; Terra, Ximena; Lih, Fred B; Beltran-Debon, Raul; Manousou, Penelopi; Purkayastha, Sanjay; Moorthy, Krishna; Thursz, Mark R; Zhang, Guodong; Goldin, Robert D; Zeldin, Darryl C; Petretto, Enrico; Behmoaras, Jacques
    Departament: Bioquímica i Biotecnologia
    Autor/s de la URV: Beltrán Debón, Raúl Alejandro / Terra Barbadora, Ximena
    Paraules clau: Tandem mass spectrometry; Ppar-gamma; Oxylipins; Obesity; Middle aged; Metabolic syndrome; Male; Liver; Insulin sensitivity; Inhibition; Inflammation; Hydrolase deficiency; Humans; Glucose-homeostasis; Female; Fatty liver; Epoxyeicosatrienoic acids; Epoxides; Diols; Dihom; Biomarkers; Adult; Adipose tissue, white; Adipogenesi; Adipocyte differentiation; 13-epome; 12,13-epome:dihome; 12
    Resum: Background Obesity drives maladaptive changes in the white adipose tissue (WAT) which can progressively cause insulin resistance, type 2 diabetes mellitus (T2DM) and metabolic dysfunction -associated liver disease (MASLD). Obesity -mediated loss of WAT homeostasis can trigger liver steatosis through dysregulated lipid pathways such as those related to polyunsaturated fatty acid (PUFA)-derived oxylipins. However, the exact relationship between oxylipins and metabolic syndrome remains elusive and cross -tissue dynamics of oxylipins are ill-de fi ned. Methods We quanti fi ed PUFA-related oxylipin species in the omental WAT, liver biopsies and plasma of 88 patients undergoing bariatric surgery (female N = 79) and 9 patients (female N = 4) undergoing upper gastrointestinal surgery, using UPLC-MS/MS. We integrated oxylipin abundance with WAT phenotypes (adipogenesis, adipocyte hypertrophy, macrophage in fi ltration, type I and VI collagen remodelling) and the severity of MASLD (steatosis, in fl ammation, fi brosis) quanti fi ed in each biopsy. The integrative analysis was subjected to (i) adjustment for known risk factors and, (ii) control for potential drug -effects through UPLC-MS/MS analysis of metformin-treated fat explants ex vivo . Findings We reveal a generalized down -regulation of cytochrome P450 (CYP)-derived diols during obesity conserved between the WAT and plasma. Notably, epoxide:diol ratio, indicative of soluble epoxide hydrolyse (sEH) activity, increases with WAT in fl ammation/ fi brosis, hepatic steatosis and T2DM. Increased 12,13-EpOME:DiHOME in WAT and liver is a marker of worsening metabolic syndrome in patients with obesity. Interpretation These fi ndings suggest a dampened sEH activity and a possible role of fatty acid diols during metabolic syndrome in major metabolic organs such as WAT and liver. They also have implications in view of the clinical trials based on sEH inhibition for metabolic syndrome.
    Àrees temàtiques: Saúde coletiva; Medicine, research & experimental; Medicine (miscellaneous); Medicine (all); Medicina iii; Medicina ii; Medicina i; General medicine; General biochemistry,genetics and molecular biology; Ciências biológicas ii; Biotecnología; Biochemistry, genetics and molecular biology (miscellaneous); Biochemistry, genetics and molecular biology (all)
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: ximena.terra@urv.cat; raul.beltran@urv.cat
    Data d'alta del registre: 2025-01-28
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(24)00162-2/fulltext
    Referència a l'article segons font original: Ebiomedicine. 103 105127-
    Referència de l'ítem segons les normes APA: Hateley, Charlotte; Olona, Antoni; Halliday, Laura; Edin, Matthew L; Ko, Jeong-Hun; Forlano, Roberta; Terra, Ximena; Lih, Fred B; Beltran-Debon, Raul; (2024). Multi-tissue pro fi ling of oxylipins reveal a conserved up-regulation of epoxide:diol ratio that associates with white adipose tissue in fl ammation and liver steatosis in obesity. Ebiomedicine, 103(), 105127-. DOI: 10.1016/j.ebiom.2024.105127
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI de l'article: 10.1016/j.ebiom.2024.105127
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2024
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Biochemistry, Genetics and Molecular Biology (Miscellaneous),Medicine (Miscellaneous),Medicine, Research & Experimental
    Tandem mass spectrometry
    Ppar-gamma
    Oxylipins
    Obesity
    Middle aged
    Metabolic syndrome
    Male
    Liver
    Insulin sensitivity
    Inhibition
    Inflammation
    Hydrolase deficiency
    Humans
    Glucose-homeostasis
    Female
    Fatty liver
    Epoxyeicosatrienoic acids
    Epoxides
    Diols
    Dihom
    Biomarkers
    Adult
    Adipose tissue, white
    Adipogenesi
    Adipocyte differentiation
    13-epome
    12,13-epome:dihome
    12
    Saúde coletiva
    Medicine, research & experimental
    Medicine (miscellaneous)
    Medicine (all)
    Medicina iii
    Medicina ii
    Medicina i
    General medicine
    General biochemistry,genetics and molecular biology
    Ciências biológicas ii
    Biotecnología
    Biochemistry, genetics and molecular biology (miscellaneous)
    Biochemistry, genetics and molecular biology (all)
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