The recent development of a novel class of insulin-sensitizing drugs, the thiazolidinediones (TZDs), represents a significant advance in antidiabetic therapy. One key mechanism by which these drugs exert their effects is by activation of the peroxisome proliferator activated receptor gamma (PPAR-gamma), a member of the nuclear receptor family. Evidence supporting this mechanism of action of the TZDs will be reviewed in this article. Recent data suggests that PPAR-gamma agonists might also have therapeutic potential in the treatment of inflammatory diseases and certain cancers.
机构:
Aston Univ, Sch Life & Hlth Sci, Diabet Res Grp, Birmingham B4 7ET, W Midlands, EnglandAston Univ, Sch Life & Hlth Sci, Diabet Res Grp, Birmingham B4 7ET, W Midlands, England
机构:
Aston Univ, Sch Life & Hlth Sci, Diabet Res Grp, Birmingham B4 7ET, W Midlands, EnglandAston Univ, Sch Life & Hlth Sci, Diabet Res Grp, Birmingham B4 7ET, W Midlands, England