From bench to bedside: novel mechanisms and therapeutic advances through the development of selective peroxisome proliferator-activated receptor γ modulators

被引:16
作者
Blackburn, George L. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Study Nutr Med, Boston, MA 02155 USA
关键词
GROWTH-FACTOR; 21; CARDIOVASCULAR EVENTS; RISK; PROTEIN;
D O I
10.3945/ajcn.2009.28449A
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
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 gamma (PPAR gamma) 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 gamma, including modes of action and recently discovered side effects of PPAR gamma 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 gamma modulators. These molecules offer a new direction in the search for more specific PPAR gamma activators that will retain efficacy for the treatment of diabetes without major side effects. Am J Clin Nutr 2010;91(suppl):251S-3S.
引用
收藏
页码:251S / 253S
页数:3
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