| Literature DB >> 31970778 |
Gabriela Viegas Haute1, Carolina Luft1,2, Géssica Luana Antunes2, Josiane Silva Silveira2, Bruno de Souza Basso1, Mariana Severo da Costa2, Vitor Giancarlo Schneider Levorse1, Daniela Benvenutti Kaiber2, Márcio Vinícius Fagundes Donadio2, Jordi Gracia-Sancho3,4, Jarbas Rodrigues de Oliveira1.
Abstract
Acute lung injury (ALI) is an inflammatory process, and has high incidence and mortality. ALI and the acute respiratory distress syndrome are two common complications worldwide that result in acute lung failure, sepsis, and death. Pro-inflammatory substances, such as cytokines and chemokines, are responsible for activating the body's defense mechanisms and usually mediate inflammatory processes. Therefore, the research of substances that decrease the uncontrolled response of organism is seen as potential for patients with ALI. Octyl gallate (OG) is a phenolic compound with therapeutic actions namely antimicrobial, antiviral, and antifungal. In this study, we evaluated its action on lipopolysaccharide (LPS)-activated alveolar macrophages RAW 264.7 cells and ALI in male mice. Our results demonstrated protective effects of OG in alveolar macrophages activated with LPS and mice with ALI. The OG treatment significantly decreased the inflammatory markers in both studies in vitro and in vivo. The data suggested that OG can act as an anti-inflammatory agent for ALI.Entities:
Keywords: acute lung injury; inflammation; macrophages; octyl gallate
Year: 2020 PMID: 31970778 DOI: 10.1002/jcp.29536
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384