脂肪生成
调节器
过氧化物酶体增殖物激活受体
Wnt信号通路
噻唑烷二酮
去氢骆驼蓬碱
生物
细胞生物学
受体
罗格列酮
核受体
药理学
脂肪组织
信号转导
生物化学
2型糖尿病
内分泌学
转录因子
基因
糖尿病
作者
Hironori Waki,Kye Won Park,Nico Mitro,Liming Pei,Robert Damoiseaux,Damien C. Wilpitz,Karen Reue,Enrique Sáez,Peter Tontonoz
出处
期刊:Cell Metabolism
[Cell Press]
日期:2007-05-01
卷期号:5 (5): 357-370
被引量:195
标识
DOI:10.1016/j.cmet.2007.03.010
摘要
PPARgamma is the master regulator of adipogenesis and the molecular target of the thiazolidinedione antidiabetic drugs. By screening for compounds that promote adipogenesis, we identified a small molecule that targets the PPARgamma pathway by a distinct mechanism. This molecule, harmine, is not a ligand for the receptor; rather, it acts as a cell-type-specific regulator of PPARgamma expression. Administration of harmine to diabetic mice mimics the effects of PPARgamma ligands on adipocyte gene expression and insulin sensitivity. Unlike thiazolidinediones, however, harmine does not cause significant weight gain or hepatic lipid accumulation. Molecular studies indicate that harmine controls PPARgamma expression through inhibition of the Wnt signaling pathway. This work validates phenotypic screening of adipocytes as a promising strategy for the identification of bioactive small molecules and suggests that regulators of PPARgamma expression may represent a complementary approach to PPARgamma ligands in the treatment of insulin resistance.
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