Changes in FGF21 serum concentrations and liver mRNA expression in an experimental model of complete lipodystrophy and insulin-resistant diabetes
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24908095
DOI
10.33549/physiolres.932714
PII: 932714
Knihovny.cz E-resources
- MeSH
- Diabetes Mellitus, Experimental metabolism MeSH
- Fibroblast Growth Factors biosynthesis blood metabolism MeSH
- Adipose Tissue, Brown metabolism MeSH
- Hypothalamus metabolism MeSH
- Insulin Resistance * MeSH
- Liver metabolism MeSH
- Lipodystrophy metabolism MeSH
- RNA, Messenger biosynthesis MeSH
- Mice MeSH
- Neuropeptides metabolism MeSH
- Pancreas metabolism MeSH
- Receptor, Fibroblast Growth Factor, Type 1 metabolism MeSH
- Spleen metabolism MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- fibroblast growth factor 21 MeSH Browser
- Fibroblast Growth Factors MeSH
- RNA, Messenger MeSH
- Neuropeptides MeSH
- Receptor, Fibroblast Growth Factor, Type 1 MeSH
Patients with obesity and type 2 diabetes often display high levels of the anti-diabetic factor fibroblast growth factor-21 (FGF21), suggesting that the overproduction of FGF21 may result from increased adiposity in an attempt by white adipose tissue (WAT) to counteract insulin resistance. However, the production of FGF21 diabetes in the absence of WAT has not been examined. In this study, we investigated the effects of lipodystrophy in A-ZIP F-1 mice on FGF21 production in relation to diabetes. A-ZIP F-1 mice displayed high FGF21 plasma levels resulting from enhanced FGF21 mRNA expression in the liver. Concomitant enhancement of FGF21 receptor (FGFR1) and glucose transporter 1 (GLUT-1) mRNA expression was observed in the muscles of A-ZIP F-1 mice. Furthermore, the activation of hypothalamic NPY and AgRP mRNA expression positively correlated with plasma levels of FGF21 but not active ghrelin. Our study demonstrates that an increased FGF21 plasma level in lipodystrophic A-ZIP F-1 mice results mainly from up-regulated liver production but does not suffice to overcome the lipodystrophy-induced severe type 2-diabetes and insulin resistance in the liver linked to the augmented liver fat deposition.
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