Mannose is an insulin-regulated metabolite reflecting whole-body insulin sensitivity in man.


Journal

Metabolism: clinical and experimental
ISSN: 1532-8600
Titre abrégé: Metabolism
Pays: United States
ID NLM: 0375267

Informations de publication

Date de publication:
01 2020
Historique:
received: 01 05 2019
revised: 06 09 2019
accepted: 14 09 2019
pubmed: 5 11 2019
medline: 28 4 2020
entrez: 5 11 2019
Statut: ppublish

Résumé

Mannose is a glucose-associated serum metabolite mainly released by the liver. Recent studies have shown several unexpected pleiotropic effects of mannose including increased regulatory T cells (Tregs), prevention of auto-immune disease and ability to reduce growth of human cancer cells. We have previously shown in large cohorts that elevated serum mannose levels are associated with future development of type 2 diabetes (T2D) and cardiovascular disease. However, potential direct effects of mannose on insulin sensitivity in vivo or in vitro are unknown. We here show that administration of mannose (0.1 g/kg BW twice daily) for one week in man did not elicit negative effects on meal-modified glucose tolerance, markers of inflammation or insulin levels. Tregs number and insulin signaling in human liver cells were unchanged. These data suggest that mannose is a marker, and not a mediator, of insulin resistance. To verify this, we examined serum mannose levels during long-term euglycemic hyperinsulinemic clamps in non-diabetic and T2D individuals. Mannose was reduced by insulin infusion in proportion to whole-body insulin sensitivity. Thus, mannose is a biomarker of insulin resistance which may be useful for the early identification of diabetic individuals with insulin resistance and increased risk of its complications.

Identifiants

pubmed: 31682799
pii: S0026-0495(19)30187-8
doi: 10.1016/j.metabol.2019.153974
pii:
doi:

Substances chimiques

Biomarkers 0
Insulin 0
Mannose PHA4727WTP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

153974

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

E Ferrannini (E)

C.N.R. Institute of Clinical Physiology, 56124 Pisa, Italy.

M Bokarewa (M)

Department of Rheumatology, University of Gothenburg, 405 30 Gothenburg, Sweden.

P Brembeck (P)

Lundberg Laboratory for Diabetes Research, Department of Molecular and Clinical Medicine, University of Gothenburg, 405 30 Gothenburg, Sweden.

R Baboota (R)

Lundberg Laboratory for Diabetes Research, Department of Molecular and Clinical Medicine, University of Gothenburg, 405 30 Gothenburg, Sweden.

S Hedjazifar (S)

Lundberg Laboratory for Diabetes Research, Department of Molecular and Clinical Medicine, University of Gothenburg, 405 30 Gothenburg, Sweden.

K Andersson (K)

Department of Rheumatology, University of Gothenburg, 405 30 Gothenburg, Sweden.

S Baldi (S)

Department of Clinical & Experimental Medicine, University of Pisa, 56124 Pisa, Italy.

B Campi (B)

C.N.R. Institute of Clinical Physiology, 56124 Pisa, Italy; Laboratory of Biochemistry, Department of Surgical, Medical, Molecular & Critical Area Pathology, University of Pisa, 56125, Italy.

E Muscelli (E)

C.N.R. Institute of Clinical Physiology, 56124 Pisa, Italy.

A Saba (A)

Laboratory of Biochemistry, Department of Surgical, Medical, Molecular & Critical Area Pathology, University of Pisa, 56125, Italy.

I Sterner (I)

Lundberg Laboratory for Diabetes Research, Department of Molecular and Clinical Medicine, University of Gothenburg, 405 30 Gothenburg, Sweden.

C Wasen (C)

Department of Rheumatology, University of Gothenburg, 405 30 Gothenburg, Sweden.

U Smith (U)

Lundberg Laboratory for Diabetes Research, Department of Molecular and Clinical Medicine, University of Gothenburg, 405 30 Gothenburg, Sweden. Electronic address: ulf.smith@medic.gu.se.

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Classifications MeSH