The usefulness of anti-inflammatory drugs as an adjunct
therapy to improve outcomes in
COVID-19 patients is intensely discussed in this paper.
Willow bark (Salix cortex) has been used for centuries to relieve
pain,
inflammation, and
fever. Its main active ingredient,
salicin, is metabolized in the human body into
salicylic acid, the precursor of the commonly used
pain drug acetylsalicylic acid (ASA). Here, we report on the in vitro anti-inflammatory efficacy of two methanolic Salix extracts, standardized to phenolic compounds, in comparison to ASA in the context of a SARS-CoV-2
peptide challenge. Using SARS-CoV-2
peptide/IL-1β- or LPS-activated human PBMCs and an inflammatory intestinal Caco-2/HT29-MTX co-culture, Salix extracts, and ASA concentration-dependently suppressed
prostaglandin E2 (
PGE2), a principal mediator of
inflammation. The inhibition of COX-2
enzyme activity, but not
protein expression was observed for ASA and one Salix extract. In activated PBMCs, the suppression of relevant
cytokines (i.e., IL-6, IL-1β, and IL-10) was seen for both Salix extracts. The anti-inflammatory capacity of Salix extracts was still retained after transepithelial passage and liver cell metabolism in an advanced co-culture model system consisting of intestinal Caco-2/HT29-MTX cells and differentiated hepatocyte-like HepaRG cells. Taken together, our in vitro data suggest that Salix extracts might present an additional anti-inflammatory treatment option in the context of SARS-CoV-2
peptides challenge; however, more confirmatory data are needed.