Because studies have shown that 17-estradiol (E2) produces anti-inflammatory effects after various adverse circulatory conditions, we have recently demonstrated that E2 significantly reduced the acute lung injury. Moreover, previous results suggest that peroxisome proliferator-activated receptor- (PPAR-), an intracellular transcription factor activated by fatty acids, plays a role in the control of inflammation. With the aim to characterize the role of PPAR- in estrogen-mediated anti-inflammatory activity, we tested the efficacy of E2 in an experimental model of lung inflammation, carrageenan-induced pleurisy, comparing ovariectomized wild-type (WT) and PPAR- lacking (PPAR-KO) mice. Results indicate that E2-mediated anti-inflammatory activity is weakened in PPAR-KO mice, compared with WT control groups. In particular, E2 was less effective in PPAR-KO, compared with WT mice, in inhibition of cell migration as well as lung injury, NF-kB activation, TNF- production, and inducible nitric-oxide synthase (iNOS) activation. Moreover, macrophages from PPAR-KO were less susceptible to E2- induced iNOS inhibition in vitro compared with macrophages from WT mice. Moreover, the results indicate that PPAR- was required for estrogen receptor up-regulation, following E2 treatment. These results show for the first time that PPAR- contributes to the anti-inflammatory activity of E2.
PPAR-alpha contributes to the anti-inflammatory activity of 17beta-estradiol.
BRUSCOLI, STEFANO;MIGLIORATI, Graziella;
2009
Abstract
Because studies have shown that 17-estradiol (E2) produces anti-inflammatory effects after various adverse circulatory conditions, we have recently demonstrated that E2 significantly reduced the acute lung injury. Moreover, previous results suggest that peroxisome proliferator-activated receptor- (PPAR-), an intracellular transcription factor activated by fatty acids, plays a role in the control of inflammation. With the aim to characterize the role of PPAR- in estrogen-mediated anti-inflammatory activity, we tested the efficacy of E2 in an experimental model of lung inflammation, carrageenan-induced pleurisy, comparing ovariectomized wild-type (WT) and PPAR- lacking (PPAR-KO) mice. Results indicate that E2-mediated anti-inflammatory activity is weakened in PPAR-KO mice, compared with WT control groups. In particular, E2 was less effective in PPAR-KO, compared with WT mice, in inhibition of cell migration as well as lung injury, NF-kB activation, TNF- production, and inducible nitric-oxide synthase (iNOS) activation. Moreover, macrophages from PPAR-KO were less susceptible to E2- induced iNOS inhibition in vitro compared with macrophages from WT mice. Moreover, the results indicate that PPAR- was required for estrogen receptor up-regulation, following E2 treatment. These results show for the first time that PPAR- contributes to the anti-inflammatory activity of E2.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.