mice model for studying glycation in the context of diabetes.

Guilbaud, Axel; Howsam, Michael; Niquet-Leridon, Celine; Delguste, Florian; Boulanger, Eric; Tessier, Frederic

Type de document :

Article dans une revue scientifique

DOI :

10.1002/dmrr.3103

PMID :

30467969

URL permanente :

http://hdl.handle.net/20.500.12210/4601

Titre :

mice model for studying glycation in the context of diabetes.

Auteur(s) :

Guilbaud, Axel [Auteur]
Howsam, Michael [Auteur]
Lille Inflammation Research International Center (LIRIC) - U995
Niquet-Leridon, Celine [Auteur]
Delguste, Florian [Auteur]
Boulanger, Eric [Auteur]
Lille Inflammation Research International Center (LIRIC) - U995
Tessier, Frederic [Auteur]
Lille Inflammation Research International Center (LIRIC) - U995

Titre de la revue :

Diabetes/metabolism research and reviews

Nom court de la revue :

Diabetes Metab. Res. Rev.

Pagination :

e3103

Date de publication :

2018-11-22

ISSN :

1520-7560

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

BACKGROUND: Early (furosine) and advanced (carboxymethyllysine, CML) products of glycation (AGEs) have been reported as increased in plasma, tissues, and organs of diabetic people, indicating a direct link between ...
Lire la suite >BACKGROUND: Early (furosine) and advanced (carboxymethyllysine, CML) products of glycation (AGEs) have been reported as increased in plasma, tissues, and organs of diabetic people, indicating a direct link between glycation and type 2 diabetes (T2D). While murine models present some of the characteristics observed in diabetic humans, their pertinence as models of glycation, particularly for T2D, remains poorly described. The aim of this study was to characterize and compare glycation in several organs of two commonly studied murine models of T2D using stable isotope dilution liquid chromatography tandem mass spectrometry (LC-MS/MS). METHODS: Defining parameters of type 2 diabetes including body weight, fasting glycaemia, and glucose intolerance were measured in three different C57BL6 mouse models of T2D-the genetic LepR(db/db) (db/db) model and two diet-induced obesity (DIO) models-and their respective controls. Furosine, free, and protein-bound CML were quantified in kidneys, lungs, heart, and liver by LC-MS/MS. RESULTS: The obesity, hyperglycaemia, and glucose intolerance in db/db mice was accompanied by an increase of furosine and protein-bound CML levels in all organs relative to controls. The DIO models took several months to become obese, exhibited less severe hyperglycaemia and glucose intolerance, while glycation products were not significantly different between these groups (with the exception of furosine in liver and CML in lungs). CONCLUSIONS: The db/db model better reflected the characteristics of human T2D compared with the DIO models and exhibited greater formation and accumulation of both furosine and protein-bound CML in all of the organs tested here.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

Inserm
Université de Lille
CHU Lille

Collections :

Lille Inflammation Research International Center (LIRIC) - U995

Équipe(s) de recherche :

Glycation from inflammation to aging

Date de dépôt :

2019-03-01T14:17:31Z

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