Skip to ContentSkip to Navigation
Research Pediatrics
University Medical Center Groningen

New Key Publication: Pirfenidone ameliorates pulmonary arterial pressure and neointimal remodeling in experimental pulmonary arterial hypertension by suppressing NLRP3 inflammasome activation

17 June 2022

Abstract

Pulmonary arterial hypertension (PAH) is a fatal disease characterized by increased pulmonary arterial pressure, inflammation, and neo-intimal remodeling of pulmonary arterioles. Serum levels of interleukin (IL)-1β and IL-18 are elevated in PAH patients and may enhance pro-inflammatory neo-intimal remodeling. NLRP3 inflammasome activation induces cleavage of the cytokines interleukin (IL)-1β and IL-18, required for their secretion. Pirfenidone (PFD), an anti-fibrotic and anti-inflammatory drug, has been suggested to inhibit NLRP3 inflammasome activation. We hypothesized that PFD delays the progression of PAH by suppressing NLRP3 inflammasome activation. We assessed the effects of PFD treatment in a rat model for neointimal PAH induced by monocrotaline and aortocaval shunt using echocardiographic, hemodynamic, and vascular remodeling parameters. We measured inflammasome activation by NLRP3 immunostaining, Western blots for caspase-1, IL-1β, and IL-18 cleavage, and macrophage IL-1β secretion. PFD treatment ameliorated pulmonary arterial pressure (mPAP), pulmonary vascular resistance, and pulmonary vascular remodeling in PAH rats. In PAH rats, immunostaining of NLRP3 in pulmonary arterioles and caspase-1, IL-1β, and IL-18 cleavage in lung homogenates were increased compared to controls, reflecting NLRP3 inflammasome activation in vivo. PFD decreased IL-1β and IL-18 cleavage, as well as macrophage IL-1β secretion in vitro. Our studies show that PFD ameliorates pulmonary hemodynamics and vascular remodeling in experimental PAH. While PFD did not affect all NLRP3 inflammasome parameters, it decreased IL-1β and IL-18 cleavage, the products of NLRP3 inflammasome activation that are key to its downstream effects. Our findings thus suggest therapeutic benefit of PFD in PAH via suppression of NLRP3 inflammasome activation.

Authors:

  • Emmanouil Mavrogiannis
  • Quint A.J. Hagdorn
  • Venetia Bazioti
  • Johannes M. Douwes
  • Diederik E. van der Feen
  • Silke U. Oberdorf-Maass
  • Marit Westerterp
  • Rolf M.F. Berger

Pulmonary Circulation: https://onlinelibrary.wiley.com/doi/abs/10.1002/pul2.12101

highlight in 'Rare Disease Advisor' : https://www.rarediseaseadvisor.com/news/pah-news-briefs/pirfenidone-delays-pah-progression-in-rodent-model/

Last modified:24 June 2022 11.24 a.m.

More news

  • 16 April 2024

    UG signs Barcelona Declaration on Open Research Information

    In a significant stride toward advancing responsible research assessment and open science, the University of Groningen has officially signed the Barcelona Declaration on Open Research Information.

  • 02 April 2024

    Flying on wood dust

    Every two weeks, UG Makers puts the spotlight on a researcher who has created something tangible, ranging from homemade measuring equipment for academic research to small or larger products that can change our daily lives. That is how UG...

  • 18 March 2024

    VentureLab North helps researchers to develop succesful startups

    It has happened to many researchers. While working, you suddenly ask yourself: would this not be incredibly useful for people outside of my own research discipline? There are many ways to share the results of your research. For example, think of a...