Integrating 16S rRNA Sequencing, Microflora Metabolism, and Network Pharmacology to Investigate the Mechanism of SBL in Alleviating HDM-Induced Allergic Rhinitis.
Peiting LiSharon Sze-Man HonMiranda Sin-Man TsangLea Ling-Yu KanAndrea Yin-Tung LaiBen Chung Lap ChanPing Chung LeungChun-Kwok WongPublished in: International journal of molecular sciences (2024)
Allergic rhinitis (AR) is a series of allergic reactions to allergens in the nasal mucosa and is one of the most common allergic diseases that affect both children and adults. Shi-Bi-Lin (SBL) is the modified formula of Cang Er Zi San (CEZS), a traditional Chinese herbal formula used for treating AR. Our study aims to elucidate the anti-inflammatory effects and mechanisms of SBL in house dust mite-induced AR by regulating gut microflora metabolism. In vivo studies showed that nasal allergies and the infiltration of inflammatory cells in the nasal epithelium were significantly suppressed by SBL. Moreover, SBL restored the impaired nasal epithelial barrier function with an increased tight junction protein expression and reduced the endothelial nitric oxide synthase (eNOS). Interestingly, SBL significantly reconstituted the abundance and composition of gut microbiota in AR mice; it increased the relative abundance of potentially beneficial genera and decreased the relative abundance of harmful genera. SBL also restored immune-related metabolisms, which were significantly increased and correlated with suppressing inflammatory cytokines. Furthermore, a network analysis and molecular docking indicated IL-6 was a possible target drug candidate for the SBL treatment. SBL dramatically reduced the IL-6 level in the nasal lavage fluid (NALF), suppressing the IL-6 downstream Erk1/2 and AKT/PI3K signaling pathways. In conclusion, our study integrates 16S rRNA sequencing, microflora metabolism, and network pharmacology to explain the immune mechanism of SBL in alleviating HDM-induced allergic rhinitis.
Keyphrases
- allergic rhinitis
- signaling pathway
- molecular docking
- nitric oxide synthase
- high glucose
- network analysis
- chronic rhinosinusitis
- endothelial cells
- induced apoptosis
- diabetic rats
- pi k akt
- nitric oxide
- drug induced
- antibiotic resistance genes
- emergency department
- risk assessment
- metabolic syndrome
- molecular dynamics simulations
- wastewater treatment
- microbial community
- cell cycle arrest
- case control
- anaerobic digestion
- health risk