Polyphenols from alleviated acute lung injury in rats by inhibiting oxidative stress sensitive pathways.

Objective: is a medicinal plant frequently used in the treatment of inflammatory diseases in south China. In this study, we aimed to explore its bioactive constituent which contributes to the anti-inflammatory activity.

Methods: Polyphenol-enriched and polyphenol-deprived fractions (PRF and PDF, respectively) were separated from the ethanolic extract by HPD300 macroporous resin-based method, and their anti-inflammatory activities were investigated on a lipopolysaccharide (LPS)-induced acute lung injury (ALI) model in rats. The possible mechanism of action in alleviating acute inflammation was studied using RAW264.7 cells.

Results: Both Folin-Ciocalteu and H nuclear magnetic resonance (NMR) analyses showed that polyphenolic content in PRF was approximately 10 times higher than that of PDF, and this observation reflected in their antioxidative capacities. PRF but not PDF significantly decreased the level of malondialdehyde, suppressed the expression of nicotinamide phosphoribosyltransferase (NAMPT) protein, and improved the severity of ALI in rats. PRF at 10 μg/mL effectively downregulated the expression of proteins NAMPT, HMGB1, TLR4, and p-p65, and scavenged the intracellular reactive oxygen species (ROS) in LPS-primed RAW264.7 cells. -acetyl--cysteine exhibited similar inhibitory effects on ROS production and NAMPT-mediated TLR4/NF-κB activation , whereas nicotinamide mononucleotide antagonized all the changes induced by PRF during cotreatments.

Conclusion: As an antioxidant, PRF exhibited potent anti-inflammatory activity under both and conditions by downregulating NAMPT and TLR4/NF-κB. Accordingly, polyphenols were identified as important bioactive constituents in targeting oxidative stress-sensitive pro-inflammatory pathways.