Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors,
which heterodimerize with the retinoid X receptor and bind to peroxisome pr
oliferator response elements in the promoters of regulated genes. Despite t
he wealth of information available on the function of PPAR alpha and PPAR g
amma, relatively little is known about the most widely expressed PPAR subty
pe, PPAR delta. Here we show that treatment of insulin resistant db/db mice
with the PPAR delta agonist L-165041, at doses that had no effect on eithe
r glucose or triglycerides, raised total plasma cholesterol concentrations.
The increased cholesterol was primarily associated,vith high density lipop
rotein (HDL) particles, as shown by fast protein liquid chromatography anal
ysis. These data,were corroborated by the chemical analysis of the lipoprot
eins isolated by ultracentrifugation, demonstrating that treatment with L-1
65041 produced an increase in circulating HDL without major changes in very
low or low density lipoproteins. White adipose tissue lipoprotein lipase a
ctivity,vas reduced following treatment with the PPAR delta ligand, but was
increased by a PPAR gamma agonist. These data suggest both that PPAR delta
is involved in the regulation of cholesterol metabolism in db/db mice and
that PPAR delta ligands could potentially have therapeutic value. (C) 2000
Federation of European Biochemical Societies.