help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Endocrinology, doi:10.1210/en.2003-1671
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
145/6/2594    most recent
Author Manuscript (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fu, L.
Right arrow Articles by Stewart, T. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fu, L.
Right arrow Articles by Stewart, T. A.
Endocrinology Vol. 145, No. 6 2594-2603
Copyright © 2004 by The Endocrine Society

Fibroblast Growth Factor 19 Increases Metabolic Rate and Reverses Dietary and Leptin-Deficient Diabetes

Ling Fu, Linu M. John, Sean H. Adams, Xing Xian Yu, Elizabeth Tomlinson, Mark Renz, P. Mickey Williams, Robert Soriano, Racquel Corpuz, Barbara Moffat, Richard Vandlen, Laura Simmons, Jessica Foster, Jean-Philippe Stephan, Siao Ping Tsai and Timothy A. Stewart

Departments of Molecular Biology (L.F., L.M.J., E.T., M.R., L.S., J.F., T.A.S.), Protein Engineering (R.C., B.M., R.V.), and Assay Technologies (J.-P.S., S.P.T.), Genentech, Inc., South San Francisco, California 94080

Address all correspondence and requests for reprints to: Timothy A. Stewart, Genentech Inc., 1 DNA Way, South San Francisco, California 94080. E-mail: timstewart{at}yahoo.com.

Hormonal control of metabolic rate can be important in regulating the imbalance between energy intake and expenditure that underlies the development of obesity. In mice fed a high-fat diet, human fibroblast growth factor 19 (FGF19) increased metabolic rate [1.53 ± 0.06 liters O2/h·kg0.75 (vehicle) vs. 1.93 ± 0.05 liters O2/h·kg0.75 (FGF19); P < 0.001] and decreased respiratory quotient [0.82 ± 0.01 (vehicle) vs. 0.80 ± 0.01 (FGF19); P < 0.05]. In contrast to the vehicle-treated mice that gained weight (0.14 ± 0.05 g/mouse·d), FGF19-treated mice lost weight (–0.13 ± 0.03 g/mouse·d; P < 0.001) without a significant change in food intake. Furthermore, in addition to a reduction in weight gain, treatment with FGF19 prevented or reversed the diabetes that develops in mice made obese by genetic ablation of brown adipose tissue or genetic absence of leptin. To explore the mechanisms underlying the FGF19-mediated increase in metabolic rate, we profiled the FGF19-induced gene expression changes in the liver and brown fat. In brown adipose tissue, chronic exposure to FGF19 led to a gene expression profile that is consistent with activation of this tissue. We also found that FGF19 acutely increased liver expression of the leptin receptor (1.8-fold; P < 0.05) and decreased the expression of acetyl coenzyme A carboxylase 2 (0.6-fold; P < 0.05). The gene expression changes were consistent with the experimentally determined increase in fat oxidation and decrease in liver triglycerides. Thus, FGF19 is able to increase metabolic rate concurrently with an increase in fatty acid oxidation.




This article has been cited by other articles:


Home page
J. Lipid Res.Home page
S. Talukdar, S. Bhatnagar, S. Dridi, and F. B. Hillgartner
Chenodeoxycholic acid suppresses the activation of acetyl-coenzyme A carboxylase-{alpha} gene transcription by the liver X receptor agonist T0-901317
J. Lipid Res., December 1, 2007; 48(12): 2647 - 2663.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
X. Wu, H. Ge, J. Gupte, J. Weiszmann, G. Shimamoto, J. Stevens, N. Hawkins, B. Lemon, W. Shen, J. Xu, et al.
Co-receptor Requirements for Fibroblast Growth Factor-19 Signaling
J. Biol. Chem., October 5, 2007; 282(40): 29069 - 29072.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
X. Huang, C. Yang, Y. Luo, C. Jin, F. Wang, and W. L. McKeehan
FGFR4 Prevents Hyperlipidemia and Insulin Resistance but Underlies High-Fat Diet Induced Fatty Liver
Diabetes, October 1, 2007; 56(10): 2501 - 2510.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
B. C. Lin, M. Wang, C. Blackmore, and L. R. Desnoyers
Liver-specific Activities of FGF19 Require Klotho beta
J. Biol. Chem., September 14, 2007; 282(37): 27277 - 27284.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
G. Aslanidi, V. Kroutov, G. Philipsberg, K. Lamb, M. Campbell-Thompson, G. A. Walter, S. Kurenov, J. Ignacio Aguirre, P. Keller, K. Hankenson, et al.
Ectopic expression of Wnt10b decreases adiposity and improves glucose homeostasis in obese rats
Am J Physiol Endocrinol Metab, September 1, 2007; 293(3): E726 - E736.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
H. D. Sun, M. Malabunga, J. R. Tonra, R. DiRenzo, F. E. Carrick, H. Zheng, H.-R. Berthoud, O. P. McGuinness, J. Shen, P. Bohlen, et al.
Monoclonal antibody antagonists of hypothalamic FGFR1 cause potent but reversible hypophagia and weight loss in rodents and monkeys
Am J Physiol Endocrinol Metab, March 1, 2007; 292(3): E964 - E976.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
A. Kharitonenkov, V. J. Wroblewski, A. Koester, Y.-F. Chen, C. K. Clutinger, X. T. Tigno, B. C. Hansen, A. B. Shanafelt, and G. J. Etgen
The Metabolic State of Diabetic Monkeys Is Regulated by Fibroblast Growth Factor-21
Endocrinology, February 1, 2007; 148(2): 774 - 781.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
W. Wente, A. M. Efanov, M. Brenner, A. Kharitonenkov, A. Koster, G. E. Sandusky, S. Sewing, I. Treinies, H. Zitzer, and J. Gromada
Fibroblast Growth Factor-21 Improves Pancreatic {beta}-Cell Function and Survival by Activation of Extracellular Signal-Regulated Kinase 1/2 and Akt Signaling Pathways
Diabetes, September 1, 2006; 55(9): 2470 - 2478.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
A. Gutierrez, E. P. Ratliff, A. M. Andres, X. Huang, W. L. McKeehan, and R. A. Davis
Bile Acids Decrease Hepatic Paraoxonase 1 Expression and Plasma High-Density Lipoprotein Levels Via FXR-Mediated Signaling of FGFR4
Arterioscler. Thromb. Vasc. Biol., February 1, 2006; 26(2): 301 - 306.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. Yu, F. Wang, C. Jin, X. Huang, and W. L. McKeehan
Independent Repression of Bile Acid Synthesis and Activation of c-Jun N-terminal Kinase (JNK) by Activated Hepatocyte Fibroblast Growth Factor Receptor 4 (FGFR4) and Bile Acids
J. Biol. Chem., May 6, 2005; 280(18): 17707 - 17714.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
A. M. Strack and R. W. Myers
Modulation of Metabolic Syndrome by Fibroblast Growth Factor 19 (FGF19)?
Endocrinology, June 1, 2004; 145(6): 2591 - 2593.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2004 by The Endocrine Society