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A single dose of angiotensin-(1-7) resolves eosinophilic inflammation and protects the lungs from a secondary inflammatory challenge.
Magalhaes, Giselle Santos; Gregorio, Juliana Fabiana; Beltrami, Vinicius Amorim; Felix, Franciel Batista; Oliveira-Campos, Livia; Bonilha, Caio Santos; Righetti, Renato Fraga; Tibério, Iolanda de Fátima Lopes Calvo; De Sousa, Frederico B; Rezende, Barbara Maximino; Teixeira-Carvalho, Andréa; Santos, Robson As; Campagnole-Santos, Maria José; Rodrigues-Machado, Maria da Gloria; Teixeira, Mauro Martins; Pinho, Vanessa.
Afiliação
  • Magalhaes GS; René Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, MG, Brazil.
  • Gregorio JF; Department of Physiology and Biophysics, National Institute of Science and Technology in Nanobiopharmaceutics, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Beltrami VA; Department of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av Antonio Carlos, 6627-ICB, Belo Horizonte, MG, 31270-901, Brazil.
  • Felix FB; Department of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av Antonio Carlos, 6627-ICB, Belo Horizonte, MG, 31270-901, Brazil.
  • Oliveira-Campos L; Medical Sciences Faculty of Minas Gerais, Post-Graduate Program in Health Sciences, Alameda Ezequiel Dias, 275, Belo Horizonte, MG, 30130-110, Brazil.
  • Bonilha CS; Center for Research in Inflammatory Diseases, University of São Paulo, São Paulo, SP, Brazil.
  • Righetti RF; Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, G12 8TA, UK.
  • Tibério IFLC; Faculty of Medicine FMUSP, University of São Paulo, São Paulo, SP, Brazil.
  • De Sousa FB; Rehabilitation Service, Hospital Sírio-Libanês, São Paulo, SP, Brazil.
  • Rezende BM; Rehabilitation Service, Hospital Sírio-Libanês, São Paulo, SP, Brazil.
  • Teixeira-Carvalho A; Laboratory of Polymeric and Supramolecular Systems, Institute of Physics and Chemistry, Federal University of Itajuba, Itajubá, MG, Brazil.
  • Santos RA; Department of Basic Nursing, School of Nursing, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Campagnole-Santos MJ; René Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, MG, Brazil.
  • Rodrigues-Machado MDG; Department of Physiology and Biophysics, National Institute of Science and Technology in Nanobiopharmaceutics, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Teixeira MM; Department of Physiology and Biophysics, National Institute of Science and Technology in Nanobiopharmaceutics, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Pinho V; Medical Sciences Faculty of Minas Gerais, Post-Graduate Program in Health Sciences, Alameda Ezequiel Dias, 275, Belo Horizonte, MG, 30130-110, Brazil. maria.machado@cienciasmedicasmg.edu.br.
Inflamm Res ; 73(6): 1019-1031, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38656426
ABSTRACT

OBJECTIVE:

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.

METHODS:

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.

RESULTS:

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.

CONCLUSION:

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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Angiotensina I / Ovalbumina / Lipopolissacarídeos / Pulmão Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Angiotensina I / Ovalbumina / Lipopolissacarídeos / Pulmão Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article