Inflammation is a key driver of immune responses; however, its dysregulation can lead to chronic diseases such as inflammatory bowel disease (IBD). This study investigates the anti-inflammatory and antioxidant effects of Jiang-Huang-Qing-Yan-Yin (JHQYY), a multi-component herbal formula, using network pharmacology, molecular docking and cellular verification. Network pharmacology identified the main active ingredients: Tea polyphenols, vitamin E, vitamin C and caffeine, as well as their associated targets in JHQYY, revealing 44 compounds and 850 potential targets. Among these, 64 common targets were identified between JHQYY and IBD. Protein-protein interaction (PPI) network analysis highlighted key targets, including IL-6, TNF, ALB, and IL1B, which are critical in the pathogenesis of IBD. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses identified significant inflammatory and immune regulatory pathways, particularly the NF-κB and IL-17 signaling pathways. Molecular docking further confirmed that key active components, such as tea polyphenols and caffeine, exhibit strong interactions with inflammatory targets like TNF and ALB. JHQYY displayed strong antioxidant activity, with the aqueous extract showing superior ABTS radical scavenging capacity, while the alcohol extract demonstrated higher ferric-reducing antioxidant power (FRAP). Additionally, the cellular experiments demonstrated that JHQYY exhibited low cytotoxicity in RAW264.7 macrophages, significantly inhibited lactate dehydrogenase (LDH) release, and reduced the expression levels of pro-inflammatory cytokines (IL-1β, IL-6, TNF-α) induced by lipopolysaccharide (LPS). This research emphasizes that JHQYY has the potential to act as a natural anti-inflammatory substance and provides preliminary in vitro evidence supporting its anti-inflammatory potential relevant to IBD.

XingQiChuShiYin (XQCSY), a conventional Chinese medicine dietary therapy, is effective in preventing non-alcoholic fatty liver disease (NAFLD), but its effective constituents and functional mechanisms are yet vague for the reason conventional modes are not suitable. Therefore, this study is centered on exploring the NAFLD prevention mechanisms of XQCSY via an in-silico method. The potential targets of XQCSY and NAFLD are obtained from public databases, and there are 81 intersected targets. Then six key targets including RAC-alpha serine/threonine-protein kinase, tumor necrosis factor, interleukin-6, interleukin-1 beta, cellular tumor antigen p53, and epidermal growth factor receptor are screened from the “herb-compound-common target” network. Subsequently, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis reveals that 513 of biological processes, 51 of cellular components, and 90 of molecular functions in XQCSY are related to the treatment of NAFLD. Results from network pharmacology show that XQCSY plays a pivotal role in preventing NAFLD with a “multicomponent-multitarget-multichannel” mechanism. Molecular docking also confirms active ingredients from XQCSY are well affinitive to the key genes and thus greatly affect NAFLD prevention. In conclusion, this research may provide a vital theoretical basis for determining the prevention mechanism of XQCSY on NAFLD.