AI Article Synopsis

  • Glucocorticoids, particularly fluticasone propionate (FP), are effective in treating nasal polyps, with their mechanisms still being studied.
  • An in vitro study evaluated FP's ability to inhibit inflammation caused by TNF-alpha in nasal polyp fibroblasts, measuring the effects on specific molecules and NF-kappaB nuclear translocation.
  • Results showed that FP reduced inflammation markers in a dose-dependent manner and decreased NF-kappaB translocation, highlighting its role in modulating inflammation in nasal polyps.

Article Abstract

Unlabelled: Glucocorticoids are considered the main treatment option for nasal polyps, but their effect is only recently being understood.

Aim: To evaluate whether fluticasone propionate (FP) inhibits the inflammatory process induced by TNF-alpha in vitro, and to assess if NF-kappaB is associated to this inhibition.

Study Design: Experimental in vitro study.

Materials And Methods: Nasal polyp fibroblasts were cultured during 24 hours. Three different concentrations of FP (1, 10 and 100 nM, added to TNF-alpha) were compared to negative (without additive) and positive (TNF-alpha) controls. Gene expression (RTQ-PCR) and protein concentration (ELISA) of VCAM-1, ICAM-1, eotaxin and RANTES were measured, as well as the nuclear translocation of NF-kappaB.

Results: TNF-alpha significantly increased protein concentration and RNA expression of all the studied molecules, as well as the nuclear translocation of NF-kappaB, when compared to the negative control. FP decreased these parameters in a dose-dependent manner, statistically different from positive control up to 100nM.

Conclusions: FP extensively inhibited inflammatory recruiters, at both protein and RNA levels, confirming the ability of glucocorticoids to modulate the inflammatory process in nasal polyps. This inhibition was associated to decreased NF-kappaB nuclear translocation, demonstrating that this is an important mechanism of glucocorticoids action for nasal polyps.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443771PMC
http://dx.doi.org/10.1590/s1808-86942011000500012DOI Listing

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