Changes in FGF21 serum concentrations and liver mRNA expression in an experimental model of complete lipodystrophy and insulin-resistant diabetes
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24908095
DOI
10.33549/physiolres.932714
PII: 932714
Knihovny.cz E-zdroje
- MeSH
- experimentální diabetes mellitus metabolismus MeSH
- fibroblastové růstové faktory biosyntéza krev metabolismus MeSH
- hnědá tuková tkáň metabolismus MeSH
- hypothalamus metabolismus MeSH
- inzulinová rezistence * MeSH
- játra metabolismus MeSH
- lipodystrofie metabolismus MeSH
- messenger RNA biosyntéza MeSH
- myši MeSH
- neuropeptidy metabolismus MeSH
- pankreas metabolismus MeSH
- receptor fibroblastových růstových faktorů, typ 1 metabolismus MeSH
- slezina metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- fibroblast growth factor 21 MeSH Prohlížeč
- fibroblastové růstové faktory MeSH
- messenger RNA MeSH
- neuropeptidy MeSH
- receptor fibroblastových růstových faktorů, typ 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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