Serum concentrations and tissue expression of a novel endocrine regulator fibroblast growth factor-21 in patients with type 2 diabetes and obesity

被引:244
作者
Mraz, M. [1 ]
Bartlova, M. [1 ]
Lacinova, Z. [1 ]
Michalsky, D. [2 ]
Kasalicky, M. [2 ]
Haluzikova, D. [3 ]
Matoulek, M. [1 ]
Dostalova, I. [1 ]
Humenanska, V. [4 ]
Haluzik, M. [1 ]
机构
[1] First Fac Med, Dept Med 3, Prague 12808 2, Czech Republic
[2] First Fac Med, Dept Surg, Prague 12808 2, Czech Republic
[3] First Fac Med, Dept Sports Med, Prague 12808 2, Czech Republic
[4] Bio Vendor, Brno, Czech Republic
关键词
BETA-CELL FUNCTION; PPAR-ALPHA; INSULIN-RESISTANCE; METABOLIC SYNDROME; ADIPOSE-TISSUE; FIBROBLAST-GROWTH-FACTOR-21; FGF-21; HOMEOSTASIS; ADIPONECTIN; HORMONES;
D O I
10.1111/j.1365-2265.2008.03502.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Fibroblast growth factor-21 (FGF21) is a novel endocrine and paracrine regulator of metabolic homeostasis. The aim of our study was to measure its serum concentrations in patients with obesity, obesity and type 2 diabetes mellitus (T2DM) and healthy subjects (C), and to assess the changes of its circulating levels and mRNA expression after dietary and pharmacological interventions. Design We measured biochemical parameters, serum FGF21, adiponectin, leptin and insulin levels by commercial ELISA and RIA kits, and mRNA expression in the liver, subcutaneous and visceral fat by RT PCR in 26 obese patients, 11 T2DM patients and 32 control subjects. The interventions were acute hyperinsulinaemia during isoglycaemic-hyperinsulinaemic clamp, very low calorie diet (VLCD) and 3 months treatment with PPAR-alpha agonist fenofibrate. Results Baseline serum FGF21 levels were significantly higher in both obese and T2DM patients relative to healthy controls. FGF21 levels in obesity did not significantly differ from T2DM group. Both 3 weeks of VLCD and 3 months of fenofibrate treatment significantly increased FGF21 levels. FGF21 mRNA expression in visceral fat was twofold higher in obesity relative to C group, while it did not differ in subcutaneous fat. VLCD significantly increased FGF21 mRNA expression in subcutaneous fat of obesity. 3-h hyperinsulinaemia during the clamp increased FGF21 levels in T2DM but not in C group. Conclusion An increase in FGF21 levels after VLCD and fenofibrate treatment may contribute to positive metabolic effect of these interventions and suggests the possibility of direct positive metabolic effects of FGF21 in humans.
引用
收藏
页码:369 / 375
页数:7
相关论文
共 27 条
[11]   Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis [J].
Inagaki, T ;
Choi, M ;
Moschetta, A ;
Peng, L ;
Cummins, CL ;
McDonald, JG ;
Luo, G ;
Jones, SA ;
Goodwin, B ;
Richardson, JA ;
Gerard, RD ;
Repa, JJ ;
Mangelsdorf, DJ ;
Kliewer, SA .
CELL METABOLISM, 2005, 2 (04) :217-225
[12]   Endocrine regulation of the fasting response by PPARα-mediated induction of fibroblast growth factor 21 [J].
Inagaki, Takeshi ;
Dutchak, Paul ;
Zhao, Guixiang ;
Ding, Xunshan ;
Gautron, Laurent ;
Parameswara, Vinay ;
Li, Yong ;
Goetz, Regina ;
Mohammadi, Moosa ;
Esser, Victoria ;
Elmquist, Joel K. ;
Gerard, Robert D. ;
Burgess, Shawn C. ;
Hammer, Robert E. ;
Mangelsdorf, David J. ;
Kliewer, Steven A. .
CELL METABOLISM, 2007, 5 (06) :415-425
[13]   Evolution of the Fgf and Fgfr gene families [J].
Itoh, N ;
Ornitz, DM .
TRENDS IN GENETICS, 2004, 20 (11) :563-569
[14]   FGF-21 as a novel metabolic regulator [J].
Kharitonenkov, A ;
Shiyanova, TL ;
Koester, A ;
Ford, AM ;
Micanovic, R ;
Galbreath, EJ ;
Sandusky, GE ;
Hammond, LJ ;
Moyers, JS ;
Owens, RA ;
Gromada, J ;
Brozinick, JT ;
Hawkins, ED ;
Wroblewski, VJ ;
Li, DS ;
Mehrbod, F ;
Jaskunas, SR ;
Shanafelt, AB .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (06) :1627-1635
[15]   Fibroblast growth factor-21 as a therapeutic agent for metabolic diseases [J].
Kharitonenkov, Alexei ;
Shanafelt, Armen B. .
BIODRUGS, 2008, 22 (01) :37-44
[16]   The metabolic state of diabetic monkeys is regulated by fibroblast growth factor-21 [J].
Kharitonenkov, Alexei ;
Wroblewski, Victor J. ;
Koester, Anja ;
Chen, Yun-Fei ;
Clutinger, Cathleen K. ;
Tigno, Xenia T. ;
Hansen, Barbara C. ;
Shanafelt, Armen B. ;
Etgen, Garret J. .
ENDOCRINOLOGY, 2007, 148 (02) :774-781
[17]   Sorting out the roles of PPARα in energy metabolism and vascular horneostasis [J].
Lefebvre, P ;
Chinetti, G ;
Fruchart, JC ;
Staels, B .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (03) :571-580
[18]   PPARα is a key regulator of hepatic FGF21 [J].
Lundasen, Thomas ;
Hunt, Mary C. ;
Nilsson, Lisa-Mari ;
Sanyal, Sabyasachi ;
Angelin, Bo ;
Alexson, Stefan E. H. ;
Rudling, Mats .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 360 (02) :437-440
[19]   HOMEOSTASIS MODEL ASSESSMENT - INSULIN RESISTANCE AND BETA-CELL FUNCTION FROM FASTING PLASMA-GLUCOSE AND INSULIN CONCENTRATIONS IN MAN [J].
MATTHEWS, DR ;
HOSKER, JP ;
RUDENSKI, AS ;
NAYLOR, BA ;
TREACHER, DF ;
TURNER, RC .
DIABETOLOGIA, 1985, 28 (07) :412-419
[20]   Molecular determinants of FGF-21 activity-synergy and cross-talk with PPARγ signaling [J].
Moyers, Julie S. ;
Shiyanova, Tatiyana L. ;
Mehrbod, Farrokh ;
Dunbar, James D. ;
Noblitt, Timothy W. ;
Otto, Keith A. ;
Reifel-Miller, Anne ;
Kharitonenkov, Alexei .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 210 (01) :1-6