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Propolis reversed cigarette smoke-induced emphysema through macrophage alternative activation independent of Nrf2

Barroso, M. V., Cattani-Cavalieri, I., de Brito-Gitirana, L., Fautrel, A., Lagente, V., Schmidt, M., Porto, L. C., Romana-Souza, B., Valença, S. S. & Lanzetti, M., 15-Oct-2017, In : Bioorganic & Medicinal Chemistry. 25, 20, p. 5557-5568 12 p.

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  • Propolis reversed cigarette smoke-induced emphysema through macrophage alternative activation independent of Nrf2

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DOI

  • Marina Valente Barroso
  • Isabella Cattani-Cavalieri
  • Lycia de Brito-Gitirana
  • Alain Fautrel
  • Vincent Lagente
  • Martina Schmidt
  • Luís Cristóvão Porto
  • Bruna Romana-Souza
  • Samuel Santos Valença
  • Manuella Lanzetti

Chronic obstructive pulmonary disease (COPD) is an incurable and progressive disease. Emphysema is the principal manifestation of COPD, and the main cause of this condition is cigarette smoke (CS). Natural products have shown antioxidant and anti-inflammatory properties that can prevent acute lung inflammation and emphysema, but there are few reports in the literature regarding therapeutic approaches to emphysema. We hypothesized that supplementation with natural extracts would repair lung damage in emphysema caused by CS exposure. Mice were exposed to 60 days of CS and then treated or not with three different natural extracts (mate tea, grape and propolis) orally for additional 60 days. Histological analysis revealed significant improvements in lung histoarchitecture, with recovery of alveolar spaces in all groups treated with natural extracts. Propolis was also able to recovery alveolar septa and elastic fibers. Propolis also increased MMP-2 and decreased MMP-12 expression, favoring the process of tissue repair. Additionally, propolis recruited leukocytes, including macrophages, without ROS release. These findings led us to investigate the profile of these macrophages, and we showed that propolis could promote macrophage alternative activation, thus increasing the number of arginase-positive cells and IL-10 levels and favoring an anti-inflammatory microenvironment. We further investigated the participation of Nrf2 in lung repair, but no Nrf2 translocation to the nucleus was observed in lung cells. Proteins and enzymes related to Nrf2 were not altered, other than NQO1, which seemed to be activated by propolis in a Nrf2-independent manner. Finally, propolis downregulated IGF1 expression. In conclusion, propolis promoted lung repair in a mouse emphysema model via macrophage polarization from M1 to M2 in parallel to the downregulation of IGF1 expression in a Nrf2-independent manner. (C) 2017 Elsevier Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)5557-5568
Number of pages12
JournalBioorganic & Medicinal Chemistry
Volume25
Issue number20
Publication statusPublished - 15-Oct-2017

    Keywords

  • Propolis, Emphysema, Lung repair, M2 macrophage, Nrf2 pathway, OBSTRUCTIVE PULMONARY-DISEASE, INDUCED LUNG INJURY, GROWTH-FACTOR-I, NF-KAPPA-B, OXIDATIVE STRESS, MOUSE LUNG, INFLAMMATORY RESPONSE, EXTRACELLULAR-MATRIX, HEME OXYGENASE-1, LIVER-DISEASE

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