| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ORIGINAL RESEARCH COMMUNICATION |
modulators1,2,31 From the Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
2 Supported by the S Daniel Abraham Chair in Nutrition Medicine and the Harvard Center for Healthy Living, Harvard Medical School, Boston, MA. 3 Address correspondence to GL Blackburn, Beth Israel Deaconess Medical Center, Center for the Study of Nutrition Medicine, Feldberg 880, East Campus, 330 Brookline Avenue, Boston, MA 02155. E-mail: gblackbu{at}bidmc.harvard.edu.
Type 2 diabetes is a complex disease that requires long-term therapy aimed at multiple targets. At Experimental Biology 2009 (www.eb2009.org), held last April in New Orleans, LA, the American Society for Nutrition hosted the symposium "From bench to bedside: novel therapeutic advances through the development of selective peroxisome proliferator-activated receptor
(PPAR
) modulators." Presenters addressed the latest science on novel pathways that regulate metabolism and insulin resistance, including fibroblast growth factor 21 (FGF21) and adiponectin, as well as advances in our understanding of the biology of PPAR
, including modes of action and recently discovered side effects of PPAR
agonists. They also explored the pharmacologic and physiologic actions of FGF21 and adiponectin, metabolic regulators that could provide novel therapeutic opportunities in the future, as well as current data on selective PPAR
modulators. These molecules offer a new direction in the search for more specific PPAR
activators that will retain efficacy for the treatment of diabetes without major side effects.
This article has been cited by other articles:
![]() |
S. A Kliewer and D. J Mangelsdorf Fibroblast growth factor 21: from pharmacology to physiology Am. J. Clinical Nutrition, January 1, 2010; 91(1): 254S - 257S. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Ziemke and C. S Mantzoros Adiponectin in insulin resistance: lessons from translational research Am. J. Clinical Nutrition, January 1, 2010; 91(1): 258S - 261S. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. S. Higgins and A. M DePaoli Selective peroxisome proliferator-activated receptor {gamma} (PPAR{gamma}) modulation as a strategy for safer therapeutic PPAR{gamma} activation Am. J. Clinical Nutrition, January 1, 2010; 91(1): 267S - 272S. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. W. Cheatham Peroxisome proliferator-activated receptor translational research and clinical experience Am. J. Clinical Nutrition, January 1, 2010; 91(1): 262S - 266S. [Abstract] [Full Text] [PDF] |
||||