A single dose of angiotensin-(1–7) resolves eosinophilic inflammation and protects the lungs from a secondary inflammatory challenge

Giselle Santos Magalhaes,Juliana Fabiana Gregorio,Vinicius Amorim Beltrami, Franciel Batista Felix, Livia Oliveira-Campos,Caio Santos Bonilha,Renato Fraga Righetti, Iolanda de Fátima Lopes Calvo Tibério,Frederico B. De Sousa,Barbara Maximino Rezende, Andréa Teixeira-Carvalho, Robson AS Santos,Maria José Campagnole-Santos,Maria da Gloria Rodrigues-Machado, Mauro Martins Teixeira,Vanessa Pinho

Inflammation Research(2024)

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摘要
Angiotensin-(1–7) [Ang-(1–7)] is a pro-resolving mediator. It is not known whether the pro-resolving effects of Ang-(1–7) are sustained and protect the lung from a subsequent inflammatory challenge. This study sought to investigate the impact of treatment in face of a second allergic or lipopolysaccharide (LPS) challenge. Mice, sensitized and challenged with ovalbumin (OVA), received a single Ang-(1–7) dose at the peak of eosinophilic inflammation, 24 h after the final OVA challenge. Subsequently, mice were euthanized at 48, 72, 96, and 120 h following the OVA challenge, and cellular infiltrate, inflammatory mediators, lung histopathology, and macrophage-mediated efferocytic activity were evaluated. The secondary inflammatory stimulus (OVA or LPS) was administered 120 h after the last OVA challenge, and subsequent inflammatory analyses were performed. Treatment with Ang-(1–7) resulted in elevated levels of IL-10, CD4+Foxp3+, Mres in the lungs and enhanced macrophage-mediated efferocytic capacity. Moreover, in allergic mice treated with Ang-(1–7) and then subjected to a secondary OVA challenge, inflammation was also reduced. Similarly, in mice exposed to LPS, Ang-(1–7) effectively prevented the lung inflammation. A single dose of Ang-(1–7) resolves lung inflammation and protect the lung from a subsequent inflammatory challenge highlighting its potential therapeutic for individuals with asthma.
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关键词
Resolution of inflammation,Eosinophil,Inflammation,Ang-(1–7),Chronic inflammation
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