Methoxyeugenol Protects Against Lung Inflammation and Suppresses Neutrophil Extracellular Trap Formation in an LPS-Induced Acute Lung Injury Model.
Géssica Luana AntunesLucas Strassburger MatzenbacherBruna Pasqualotto CostaBruno de Sousa BassoVitor Giancarlo Schneider LevorseKrist Helen AntunesZaquer Suzana Munhoz Costa-FerroJarbas Rodrigues de OliveiraPublished in: Inflammation (2022)
Acute lung injury (ALI) is a life-threatening acute inflammatory disease with high rates of morbidity and mortality worldwide. 4-Allyl-2,6-dimethoxyphenol (methoxyeugenol), a phenylpropanoid from a synthetic source, exhibits strong anti-inflammatory activity, but its effects on the inflammation of ALI have not yet been reported. In our study, the anti-inflammatory effects of methoxyeugenol were investigated on RAW 264.7 cells and a mice model of ALI. Our results showed that methoxyeugenol (7.5 and 30 µM) attenuated the proliferation and gene expression of interleukin (IL)-6 in LPS-stimulated RAW 264.7 cells. In a mice model of ALI induced with LPS, methoxyeugenol exhibited a significant protective effect, based on influx reduction of macrophages and neutrophils into the lungs; reduction in release of the cytokines IL-6, TNF-α, and IL-10; and in reactive oxygen species (ROS) formation. We show that the anti-inflammatory effects of methoxyeugenol are associated with the suppression of the NFκB signaling pathway. Moreover, we demonstrated for the first time that a phenolic compound, from a synthetic source, protects against lung tissue inflammation and promotes a reduction of NET formation. These findings provided evidence for the use of methoxyeugenol as a new strategy to control inflammation in ALI disease.
Keyphrases
- lps induced
- oxidative stress
- inflammatory response
- induced apoptosis
- signaling pathway
- anti inflammatory
- gene expression
- reactive oxygen species
- lipopolysaccharide induced
- cell cycle arrest
- diabetic rats
- pi k akt
- dna damage
- epithelial mesenchymal transition
- endoplasmic reticulum stress
- cell death
- rheumatoid arthritis
- toll like receptor
- dna methylation
- intensive care unit
- liver failure
- drug induced
- hepatitis b virus
- adipose tissue
- extracorporeal membrane oxygenation
- atomic force microscopy