Despite similar clinical features metabolomics reveals distinct signatures in insulin resistant and progressively obese minipigs.


Journal

Journal of physiology and biochemistry
ISSN: 1877-8755
Titre abrégé: J Physiol Biochem
Pays: Spain
ID NLM: 9812509

Informations de publication

Date de publication:
May 2023
Historique:
received: 06 06 2022
accepted: 15 12 2022
medline: 29 6 2023
pubmed: 28 12 2022
entrez: 27 12 2022
Statut: ppublish

Résumé

Obesity is a major contributor to the silent and progressive development of type 2 diabetes (T2D) whose prevention could be improved if individuals at risk were identified earlier. Our aim is to identify early phenotypes that precede T2D in diet-induced obese minipigs. We fed four groups of minipigs (n = 5-10) either normal-fat or high-fat high-sugar diet during 2, 4, or 6 months. Morphometric features were recorded, and metabolomics and clinical parameters were assessed on fasting plasma samples. Multivariate statistical analysis on 46 morphometrical and clinical parameters allowed to differentiate 4 distinct phenotypes: NFC (control group) and three others (HF2M, HF4M, HF6M) corresponding to the different stages of the obesity progression. Compared to NFC, we observed a rapid progression of body weight and fat mass (4-, 7-, and tenfold) in obese phenotypes. Insulin resistance (IR; 2.5-fold increase of HOMA-IR) and mild dyslipidemia (1.2- and twofold increase in total cholesterol and HDL) were already present in the HF2M and remained stable in HF4M and HF6M. Plasma metabolome revealed subtle changes of 23 metabolites among the obese groups, including a progressive switch in energy metabolism from amino acids to lipids, and a transient increase in de novo lipogenesis and TCA-related metabolites in HF2M. Low anti-oxidative capacities and anti-inflammatory response metabolites were found in the HF4M, and a perturbed hexose metabolism was observed in HF6M. Overall, we show that IR and progressively obese minipigs reveal phenotype-specific metabolomic signatures for which some of the identified metabolites could be considered as potential biomarkers of early progression to TD2.

Identifiants

pubmed: 36574151
doi: 10.1007/s13105-022-00940-2
pii: 10.1007/s13105-022-00940-2
doi:

Substances chimiques

Insulin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

397-413

Subventions

Organisme : Agence Nationale de la Recherche
ID : ANR-19-CE14-0026

Informations de copyright

© 2022. The Author(s) under exclusive licence to University of Navarra.

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Auteurs

Imene Bousahba (I)

Université Clermont-Auvergne, INRAE, UMR1019, Unité Nutrition Humaine, Clermont-Ferrand, France.
UMR1331 Toxalim, Université de Toulouse, INRAE, ENVT, INP-Purpan, UPS, Toulouse, France.

Jérémie David (J)

Université Clermont-Auvergne, INRAE, UMR1019, Unité Nutrition Humaine, Clermont-Ferrand, France.

Florence Castelli (F)

CEA, INRAE, Médicaments Et Technologies Pour La Santé (MTS), Université Paris Saclay, MetaboHUB, 91191, Gif-Sur-Yvette, France.

Céline Chollet (C)

CEA, INRAE, Médicaments Et Technologies Pour La Santé (MTS), Université Paris Saclay, MetaboHUB, 91191, Gif-Sur-Yvette, France.

Sadia Ouzia (S)

CEA, INRAE, Médicaments Et Technologies Pour La Santé (MTS), Université Paris Saclay, MetaboHUB, 91191, Gif-Sur-Yvette, France.

François Fenaille (F)

CEA, INRAE, Médicaments Et Technologies Pour La Santé (MTS), Université Paris Saclay, MetaboHUB, 91191, Gif-Sur-Yvette, France.

Didier Rémond (D)

Université Clermont-Auvergne, INRAE, UMR1019, Unité Nutrition Humaine, Clermont-Ferrand, France.

Nathalie Poupin (N)

UMR1331 Toxalim, Université de Toulouse, INRAE, ENVT, INP-Purpan, UPS, Toulouse, France.

Sergio Polakof (S)

Université Clermont-Auvergne, INRAE, UMR1019, Unité Nutrition Humaine, Clermont-Ferrand, France. sergio.polakof@inrae.fr.

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