Anadenanthera colubrina regulated LPS-induced inflammation by suppressing NF-κB and p38-MAPK signaling pathways

We aimed to determine the chemical profile and unveil Anadenanthera colubrina (Vell.) Brenan standardized extract effects on inflammatory cytokines expression and key proteins from immunoregulating signaling pathways on LPS-induced THP-1 monocyte. Using the RT-PCR and Luminex Assays, we planned to show the gene expression and the levels of IL-8, IL-1 beta, and IL-10 inflammatory cytokines. Key proteins of NF-kappa B and MAPK transduction signaling pathways (NF-kappa B, p-38, p-NF-kappa B, and p-p38) were detected by Simple Western. Using HPLC-ESI-MSn (High-Performance Liquid-Chromatography) and HPLC-HRESIMS, we showed the profile of the extract that includes an opus of flavonoids, including the catechins, quercetin, kaempferol, and the proanthocyanidins. Cell viability was unaffected up to 250 mu g/mL of the extract (LD50 = 978.7 mu g/mL). Thereafter, the extract's impact on the cytokine became clear. Upon LPS stimuli, in the presence of the extract, gene expression of IL-1 beta and IL-10 were downregulated and the cytokines expression of IL-1 beta and IL-10 were down an upregulated respectively. The extract is involved in TLR-4-related NF-kappa B/MAPK pathways; it ignited phosphorylation of p38 and NF-kappa B, orchestrating a reduced signal intensity. Therefore, Anadenanthera colubrina's showed low cytotoxicity and profound influence as a protector against the inflammation, modulating IL-1 beta and IL-10 inflammatory cytokines gene expression and secretion by regulating intracellular NF-kappa B and p38-MAPK signaling pathways.