Protection Against Insulin Resistance by Apolipoprotein M/Sphingosine-1-Phosphate.
Adult
Animals
Apolipoproteins M
/ genetics
Blood Glucose
Body Mass Index
Diabetes Mellitus, Type 2
/ metabolism
Diet, High-Fat
Dietary Fats
/ administration & dosage
Female
Gene Expression Regulation
/ drug effects
Glycated Hemoglobin
Hep G2 Cells
Humans
Insulin Resistance
Lipid Metabolism
Lipids
/ chemistry
Liver
/ chemistry
Lysophospholipids
/ genetics
Male
Metabolome
Mice
Mice, Knockout
Middle Aged
Sphingosine
/ analogs & derivatives
Journal
Diabetes
ISSN: 1939-327X
Titre abrégé: Diabetes
Pays: United States
ID NLM: 0372763
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
received:
14
08
2019
accepted:
02
01
2020
pubmed:
10
1
2020
medline:
28
10
2020
entrez:
10
1
2020
Statut:
ppublish
Résumé
Subjects with low serum HDL cholesterol levels are reported to be susceptible to diabetes, with insulin resistance believed to be the underlying pathological mechanism. Apolipoprotein M (apoM) is a carrier of sphingosine-1-phosphate (S1P), a multifunctional lipid mediator, on HDL, and the pleiotropic effects of HDL are believed to be mediated by S1P. In the current study, we attempted to investigate the potential association between apoM/S1P and insulin resistance. We observed that the serum levels of apoM were lower in patients with type 2 diabetes and that they were negatively correlated with BMI and the insulin resistance index. While deletion of apoM in mice was associated with worsening of insulin resistance, overexpression of apoM was associated with improvement of insulin resistance. Presumably, apoM/S1P exerts its protective effect against insulin resistance by activating insulin signaling pathways, such as the AKT and AMPK pathways, and also by improving the mitochondrial functions through upregulation of SIRT1 protein levels. These actions of apoM/S1P appear to be mediated via activation of S1P1 and/or S1P3. These results suggest that apoM/S1P exerts protective roles against the development of insulin resistance.
Identifiants
pubmed: 31915150
pii: db19-0811
doi: 10.2337/db19-0811
doi:
Substances chimiques
APOM protein, human
0
ApoM protein, mouse
0
Apolipoproteins M
0
Blood Glucose
0
Dietary Fats
0
Glycated Hemoglobin A
0
Lipids
0
Lysophospholipids
0
sphingosine 1-phosphate
26993-30-6
Sphingosine
NGZ37HRE42
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
867-881Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2020 by the American Diabetes Association.