Terminalia ferdinandiana Exell. extracts reduce pro-inflammatory cytokine and PGE 2 secretion, decrease COX-2 expression and down-regulate cytosolic NF-κB levels.
Ian Edwin CockPublished in: Inflammopharmacology (2024)
Based on their high antioxidant capacity and noteworthy phytochemistry, Terminalia ferdinandiana fruit and leaves have attracted considerable recent interest for their therapeutic potential. Whilst those studies have reported a variety of therapeutic properties for the fruit, the anti-inflammatory potential of T. ferdinandiana has been largely neglected and the leaves have been almost completely ignored. This study investigated the immune-modulatory and anti-inflammatory properties of T. ferdinandiana fruit and leaf extracts by evaluating their inhibition of multiple pro- and anti-inflammatory cytokines and chemokines secretion in lipopolysaccharide (LPS)-stimulated and unstimulated RAW 264.7 macrophages using multiplex bead immunoassays and ELISA assays. The methanolic extracts were particularly good immune-modulators, significantly inhibiting the secretion of all the cytokines and chemokines tested. Indeed, the methanolic extracts completely inhibited IL-10, IFN-γ, IL-1β, IL-6, MCP-1, and MIP-2a secretion, and almost completely inhibited the secretion of TNF-α. In addition, the methanolic T. ferdinandiana extracts also significantly inhibited cytosolic COX-2 levels (by 87-95%) and the synthesis of the PGE 2 (by ~ 98%). In contrast, the methanolic extracts stimulated LTB 4 secretion by ~ 60-90%, whilst the aqueous extracts significantly inhibited LTB 4 secretion (by ~ 27% each). Exposure of RAW 264.7 cells to the methanolic T. ferdinandiana extracts also significantly down-regulated the cytosolic levels of NF-κB by 33-44%, indicating that the immune-modulatory and anti-inflammatory properties of the extracts may be regulated via a decrease in NF-κB transcription pathways. Taken together, these results demonstrate potent anti-inflammatory properties for the extracts and provide insights into their anti-inflammatory mechanisms.
Keyphrases
- anti inflammatory
- signaling pathway
- lps induced
- oxidative stress
- transcription factor
- inflammatory response
- rheumatoid arthritis
- risk assessment
- computed tomography
- dendritic cells
- nuclear factor
- cell proliferation
- induced apoptosis
- pi k akt
- mass spectrometry
- magnetic resonance imaging
- toll like receptor
- long non coding rna
- endoplasmic reticulum stress
- cell death
- atomic force microscopy
- high speed