Feruloylated Oligosaccharides Prevented Influenza-Induced Lung Inflammation via the RIG-I/MAVS/TRAF3 Pathway.
Li DengShu-Lei WeiLu WangJun-Qing HuangPublished in: Journal of agricultural and food chemistry (2024)
Uncontrolled inflammation contributes significantly to the mortality in acute respiratory infections. Our previous research has demonstrated that maize bran feruloylated oligosaccharides (FOs) possess notable anti-inflammatory properties linked to the NF-kB pathway regulation. In this study, we clarified that the oral administration of FOs moderately inhibited H1N1 virus infection and reduced lung inflammation in influenza-infected mice by decreasing a wide spectrum of cytokines (IFN-α, IFN-β, IL-6, IL-10, and IL-23) in the lungs. The mechanism involves FOs suppressing the transduction of the RIG-I/MAVS/TRAF3 signaling pathway, subsequently lowering the expression of NF-κB. In silico analysis suggests that FOs have a greater binding affinity for the RIG-I/MAVS signaling complex. This indicates that FOs have potential as promising targets for immune modulation. Moreover, in MAVS knockout mice, we confirmed that the anti-inflammatory function of FOs against influenza depends on MAVS. Comprehensive analysis using 16S rRNA gene sequencing and metabolite profiling techniques showed that FOs have the potential to restore immunity by modulating the gut microbiota. In conclusion, our study demonstrates that FOs are effective anti-inflammatory phytochemicals in inhibiting lung inflammation caused by influenza. This suggests that FOs could serve as a potential nutritional strategy for preventing the H1N1 virus infection and associated lung inflammation.
Keyphrases
- signaling pathway
- oxidative stress
- anti inflammatory
- pi k akt
- immune response
- diabetic rats
- epithelial mesenchymal transition
- poor prognosis
- type diabetes
- drug induced
- hepatitis b virus
- gene expression
- dendritic cells
- cardiovascular events
- skeletal muscle
- human health
- coronary artery disease
- cardiovascular disease
- risk assessment
- toll like receptor
- mass spectrometry
- respiratory failure
- nuclear factor
- copy number
- molecular docking
- transcription factor
- acute respiratory distress syndrome