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Improving hyperglycemic effect of FGF-21 is associated with alleviating inflammatory state in diabetes.
- Source :
-
International immunopharmacology [Int Immunopharmacol] 2018 Mar; Vol. 56, pp. 301-309. Date of Electronic Publication: 2018 Feb 03. - Publication Year :
- 2018
-
Abstract
- Type 2 diabetes mellitus (T2DM) is accompanied by abnormal glucose metabolism and low-grade chronic inflammation. Fibroblast growth factor 21 (FGF-21) is a novel metabolic regulator and can function as an endocrine hormone to regulate glucose and lipid metabolism. Recently, FGF-21 was found to have anti-inflammatory effect, to our knowledge, the effect of FGF-21 on inflammatory state in diabetes has not been elucidated. Here, we use db/db mice as a Type 2 diabetes model to determine whether FGF-21 alleviates inflammatory state while improves hyperglycemia. Our results demonstrated that FGF-21 not only showed potent long lasting hypoglycemic effect, but also demonstrated strong anti-inflammatory effect in the serum and white adipose tissue. Besides, in vitro experiments, insulin resistance (IR) was induced in 3T3-L1 adipocytes by treating with TNF-α. Our results showed that TNF-α impaired glucose metabolism of 3T3-L1 adipocytes but FGF-21 repressed gene expression of inflammatory factors caused by IR and consequently improved the glucose metabolism in 3T3-L1 adipocytes. Furthermore, FGF-21 ameliorated glucose uptake of TNF-α-induced IR in 3T3-L1 adipocytes by inhibiting NF-κB signaling pathway.<br /> (Copyright © 2018. Published by Elsevier B.V.)
- Subjects :
- Animals
Cell Line
Hyperglycemia
Insulin Resistance
Male
Mice
Mice, Inbred C57BL
Mice, Mutant Strains
NF-kappa B metabolism
Signal Transduction
Tumor Necrosis Factor-alpha metabolism
Adipocytes physiology
Adipose Tissue, White metabolism
Diabetes Mellitus, Type 2 metabolism
Fibroblast Growth Factors metabolism
Glucose metabolism
Inflammation metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1705
- Volume :
- 56
- Database :
- MEDLINE
- Journal :
- International immunopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 29414665
- Full Text :
- https://doi.org/10.1016/j.intimp.2018.01.048