PPAR-alpha contributes to the anti-inflammatory activity of glucocorticoids

Authors:
Cuzzocrea S, Bruscoli S, Mazzon E, Crisafulli C, Donato V, Di Paola R, Velardi E, Esposito E, Nocentini G, Riccardi C
In:
Source: Mol Pharmacol
Publication Date: (2008)
Issue: 73(2): 323-37
Research Area:
Immunotherapy / Hematology
Platform:
Nucleofector® I/II/2b
Experiment
Peritoneal macrophages were nucleofected with 2 μg of plasmid containing full-length PPAR-alpha or empty vector pSG5 or, for silencing, 1 μg of siRNA specific for PPAR-alpha or scrambled oligo. Each group was cotransfected with 2 μg of pEGFP vector to check transfection efficiency. 24 h after transfection, cells were treated with DEX (1 μM) followed 2 h later by stimulation with LPS and INF-γ. Cells were harvested 2 h after stimulation and prepared for Real Time analysis.
Abstract
Glucocorticoids (GCs) are effective anti-inflammatory agents widely used in therapeutic approach to treatment of acute and chronic inflammatory diseases. Previous results suggest that Peroxisome proliferator activated receptor alpha-alpha (PPAR-alpha), an intracellular transcription factor activated by fatty acids, plays a role in control of inflammation. With the aim to characterize the role of PPAR-alpha in GC-mediated anti-inflammatory activity, we tested the efficacy of dexamethasone (DEX), a synthetic GC specific for GR, in an experimental model of lung inflammation, carrageenan-induced pleurisy, comparing mice lacking PPAR-alpha (PPARalphaKO) with wild type (WT) mice. We also tested the possible synergism of combined treatment with DEX and clofibrate, a PPAR-alpha agonist. Results indicate that DEX-mediated anti-inflammatory activity is weakened in PPAR-alphaKO mice, as compared to WT controls, and that is increased in WT mice when combined with PPAR-alpha agonist treatment. In particular, DEX was less effective in PPAR-alphaKO, compared to WT mice, as evaluated by inhibition of NF-kB, of TNF-alpha production, of cell migration, of cycloxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) activation. Interestingly enough, macrophages from PPAR-alphaKO were less susceptible to DEX-induced COX-2 inhibition in vitro as compared to WT mice. However, PPAR-fN transfection in PPAR-alphaKO macrophages, with consequent receptor expression, resulted in reconstitution of susceptibility to DEX-induced COX-2 inhibition to levels comparable to that obtained in WT macrophages. Notably, the DEX effect on macrophages in vitro was significantly increased in WT cells when combined with PPAR-alpha agonist treatment. These results indicate that PPAR-alpha can contribute to the anti-inflammatory activity of GCs.