The Small Molecule Harmine Is an Antidiabetic Cell-Type-Specific Regulator of PPARγ Expression
2007; Cell Press; Volume: 5; Issue: 5 Linguagem: Inglês
10.1016/j.cmet.2007.03.010
ISSN1932-7420
AutoresHironori Waki, Kye Won Park, Nico Mitro, Liming Pei, Robert Damoiseaux, Damien C. Wilpitz, Karen Reue, Enrique Sáez, Peter Tontonoz,
Tópico(s)Toxin Mechanisms and Immunotoxins
ResumoPPARγ 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 PPARγ 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 PPARγ expression. Administration of harmine to diabetic mice mimics the effects of PPARγ 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 PPARγ 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 PPARγ expression may represent a complementary approach to PPARγ ligands in the treatment of insulin resistance.
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