Prophylactic and therapeutic treatment with the flavonone sakuranetin ameliorates LPS-induced acute lung injury

Author:

Bittencourt-Mernak Márcia Isabel1,Pinheiro Nathalia M.2,Santana Fernanda P. R.1,Guerreiro Marina P.1,Saraiva-Romanholo Beatriz M.234,Grecco Simone S.5,Caperuto Luciana C.1,Felizardo Raphael J. F.6,Câmara Niels O. S.267,Tibério Iolanda F. L. C.2,Martins Mílton A.2,Lago João Henrique G.5,Prado Carla M.128

Affiliation:

1. Biological Science Department, Federal University of São Paulo, Diadema, Brazil;

2. Medicine Department, School of Medicine, University of São Paulo, São Paulo, Brazil;

3. University City of São Paulo (UNICID), São Paulo, Brazil;

4. Institute of Medical Assistance to the State Public Servant of São Paulo (IAMSPE), São Paulo, Brazil;

5. Earth and Exact Science, Federal University of Brazil, São Paulo, Brazil;

6. Department of Medicine, Nephrology Division, Federal University of São Paulo, São Paulo, Brazil;

7. Immunology Department, Biological Science Institute, University of São Paulo, São Paulo, Brazil; and

8. Bioscience Department, Federal University of São Paulo, Santos, Brazil

Abstract

Sakuranetin is the main isolate flavonoid from Baccharis retusa ( Asteraceae) leaves and exhibits anti-inflammatory and antioxidative activities. Acute respiratory distress syndrome is an acute failure of the respiratory system for which effective treatment is urgently necessary. This study investigated the preventive and therapeutic effects of sakuranetin on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in mice. Animals were treated with intranasal sakuranetin 30 min before or 6 h after instillation of LPS. Twenty-four hours after ALI was induced, lung function, inflammation, macrophages population markers, collagen fiber deposition, the extent of oxidative stress, and the expression of matrix metalloprotease-9 (MMP-9), tissue inhibitor of MMP-9 (TIMP-1) and NF-κB were evaluated. The animals began to show lung alterations 6 h after LPS instillation, and these changes persisted until 24 h after LPS administration. Preventive and therapeutic treatment with sakuranetin reduced the neutrophils in the peripheral blood and in the bronchial alveolar lavage. Sakuranetin treatment also reduced macrophage populations, particularly that of M1-like macrophages. In addition, sakurnaetin treatment reduced keratinocyte-derived chemokines (IL-8 homolog) and NF-κB levels, collagen fiber formation, MMM-9 and TIMP-1-positive cells, and oxidative stress in lung tissues compared with LPS animals treated with vehicle. Finally, sakuranetin treatment also reduced total protein, and the levels of TNF-α and IL-1β in the lung. This study shows that sakuranetin prevented and reduced pulmonary inflammation induced by LPS. Because sakuranetin modulates oxidative stress, the NF-κB pathway, and lung function, it may constitute a novel therapeutic candidate to prevent and treat ALI.

Funder

São Paulo Research Foundation (FAPESP)

Ministry of Science, Technology and Innovation | Conselho Nacional de Desenvolvimento Científico e Tecnológico (National Council for Scientific and Technological Development)

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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