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Vol. 300, Issue 1, 72-77, January 2002
Expression in Hepatocytes
Department of Biochemistry, University of Saskatchewan, Saskatoon,
Saskatchewan, Canada
Peroxisome proliferator-activated receptor-
(PPAR-
) is a nuclear
receptor that is activated by the binding of an appropriate ligand.
Several studies have demonstrated that certain ligands can also induce
the expression of PPAR-
. In the present study, we examined the
mechanism whereby this induction occurs by specifically addressing
whether potentiation of the transactivation function of PPAR-
per se
leads to induction of expression. We observed that thiazolidinediones,
a group of insulin-sensitizing drugs, had differential effects, with
troglitazone inducing protein levels of PPAR-
, while rosiglitazone,
englitazone, and ciglitazone were without effect. Similarly, the
prostaglandin metabolite 15-deoxy-
12,14-prostaglandin
J2 and the potent synthetic ligand GW1929
(N-(2-benzoyl phenyl)-L-tyrosine) also had
no effect, as did ligands for other isoforms of PPAR. Since
troglitazone has antioxidant properties, we also examined the effect of
-tocopherol and observed that it induced PPAR-
expression in a
dose-dependent fashion. Finally, we found that mice fed troglitazone as
a dietary admixture displayed an up-regulation of hepatic PPAR-
mRNA
and protein, indicating that the mechanism of action is at the level of
gene expression and not protein stability. These data indicate that 1)
up-regulation of the transactivation function of PPAR-
does not
alone account for the induction of expression of PPAR-
by
troglitazone, and 2) an antioxidant-related mechanism may be involved.
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