Literature DB >> 15902306

FGF-21 as a novel metabolic regulator.

Alexei Kharitonenkov1, Tatiyana L Shiyanova, Anja Koester, Amy M Ford, Radmila Micanovic, Elizabeth J Galbreath, George E Sandusky, Lisa J Hammond, Julie S Moyers, Rebecca A Owens, Jesper Gromada, Joseph T Brozinick, Eric D Hawkins, Victor J Wroblewski, De-Shan Li, Farrokh Mehrbod, S Richard Jaskunas, Armen B Shanafelt.   

Abstract

Diabetes mellitus is a major health concern, affecting more than 5% of the population. Here we describe a potential novel therapeutic agent for this disease, FGF-21, which was discovered to be a potent regulator of glucose uptake in mouse 3T3-L1 and primary human adipocytes. FGF-21-transgenic mice were viable and resistant to diet-induced obesity. Therapeutic administration of FGF-21 reduced plasma glucose and triglycerides to near normal levels in both ob/ob and db/db mice. These effects persisted for at least 24 hours following the cessation of FGF-21 administration. Importantly, FGF-21 did not induce mitogenicity, hypoglycemia, or weight gain at any dose tested in diabetic or healthy animals or when overexpressed in transgenic mice. Thus, we conclude that FGF-21, which we have identified as a novel metabolic factor, exhibits the therapeutic characteristics necessary for an effective treatment of diabetes.

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Year:  2005        PMID: 15902306      PMCID: PMC1088017          DOI: 10.1172/JCI23606

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  42 in total

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5.  Attenuation of FGF signalling in mouse beta-cells leads to diabetes.

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6.  Cycloheximide-induced cPLA(2) activation is via the MKP-1 down-regulation and ERK activation.

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2.  Activation of the farnesoid X receptor induces hepatic expression and secretion of fibroblast growth factor 21.

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3.  Increased fibroblast growth factor 21 in obesity and nonalcoholic fatty liver disease.

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Journal:  Gastroenterology       Date:  2010-05-05       Impact factor: 22.682

4.  FGF-21 enhances islet engraftment in mouse syngeneic islet transplantation model.

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6.  Fibroblast growth factor 21 increases hepatic oxidative capacity but not physical activity or energy expenditure in hepatic peroxisome proliferator-activated receptor γ coactivator-1α-deficient mice.

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10.  Fusion of fibroblast growth factor 21 to a thermally responsive biopolymer forms an injectable depot with sustained anti-diabetic action.

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