Phyto-profiling of Bergenia ligulata rhizome extract and it’s in vitro antioxidative, anti-inflammatory and immunomodulatory potential: mechanistic insights from differential gene expression in acute inflammatory model of chicken splenocytes
摘要
Bergenia ligulata (Wall.) Engl. is recognized for its diverse medicinal properties, but its immunomodulatory effects remain underexplored. This study examines the antioxidative, immunostimulatory and anti-inflammatory efficacy of aqueous rhizome extract of Bergenia ligulata (BLE) using chicken splenocytes culture system- an approach not previously explored for Bergenia spp. BLE was analyzed using GC–MS, LC–MS, in vitro antioxidant and anti-inflammatory analyses. Its maximum non-cytotoxic dose (MNCD) in chicken splenocytes was determined through colorimetric- MTT assay. Dexamethasone (DEXA), a known corticosteroid, was used as a control in the study. BLE revealed presence of various phytochemicals through GC–MS, LC–MS analyses and significant antioxidant potential in different in vitro assays conducted. BLE showed MNCD as 200 µg/mL. BLE displayed increased lymphocyte proliferation upon mitogenic stimulation (immunopotentiating effect), whereas DEXA exhibited immunosuppressive effects. BLE exposure downregulated the pro-inflammatory mediators while upregulating the expression of IL-10 which is an important anti-inflammatory cytokine, demonstrating its potent anti-inflammatory properties. Additionally, BLE exposure up-regulated Nrf-2 level, indicating its ability to combat oxidative stress. BLE exposure significantly increased immunostimulatory mediators (NFAT-1 and -2), while DEXA caused reduction in the expression levels of these transcription factors and cytokines. In all, BLE exhibited presence of various phyochemicals and significant in vitro antioxidant, immunopotentiating and anti-inflammatory bioactivities. The findings underscore the multifaceted anti-inflammatory, immunostimulatory and antioxidant effects of BLE on chicken splenocytes, shedding light on its therapeutic potential in acute- inflammatory animal cell-culture model system induced by LPS-stimulation in chicken-splenocytes.
Graphical abstract