Xiaoqinglong decoction improves allergic rhinitis by inhibiting NLRP3-mediated pyroptosis in BALB/C mice

• Published in: Journal of ethnopharmacology 2024-03, Vol.321, p.117490-117490, Article 117490
• Main Authors: Wang, Ruizhi, Wang, Yongchun, Yang, Qintai, Liu, Jiaming, Lu, Zesheng, Xu, Weizhen, Zhu, Jinxiang, Liu, He, He, Weiping, Yan, Yajie, Ruan, Yan, Zhou, Min
• Format: Article
• Language: English
• Subjects: Animals; Disease Models, Animal; Inflammasomes - metabolism; Interleukin-13; Interleukin-4; Interleukin-5; Mice; Mice, Inbred BALB C; Molecular Docking Simulation; NLR Family, Pyrin Domain-Containing 3 Protein; Ovalbumin; Pyroptosis; Rhinitis, Allergic - drug therapy
• ISSN: 0378-8741; 1872-7573
• DOI: 10.1016/j.jep.2023.117490

Xiaoqinglong decoction (XQLD), first recorded in Shang Han Lun, is a traditional Chinese medicine prescribed for the treatment of allergic rhinitis (AR). XQLD alleviates the clinical symptoms of AR by inhibiting the occurrence of an inflammatory response, but the specific regulatory mechanism remains unclear. NLRP3-mediated pyroptosis is closely related to AR pathogenesis. Hence, this study aimed to explore the potential role of NLRP3-mediated pyroptosis pathway in the AR-associated pharmacological mechanism of XQLD. BALB/C mice models of AR was established by using ovalbumin (OVA) and aluminum hydroxide sensitization. After intragastric administration of different dosages of XQLD, nasal allergic symptoms were observed. The expression of OVA-sIgE and Th2 inflammatory factors (IL-4, IL-5, and IL-13) in serum was detected by ELISA. The histopathological morphology and expression of inflammatory factors in nasal mucosa along with pyroptosis were investigated. Molecular docking was performed to analyze the binding of representative compounds of XQLD with NLRP3. Activation of the NLRP3 inflammasome was detected by immunofluorescence and western blotting. XQLD significantly improved the nasal allergic symptoms of mice, reduced the degree of goblet cell proliferation, mast cell infiltration, and collagen fiber hyperplasia in nasal mucosa. Meanwhile, it could downregulate the expression of Th2 inflammatory factors (IL-4, IL-5, and IL-13) in serum and nasal mucosa. XQLD significantly reduced the number of GSDMD and TUNEL double-positive cells and IL-1β and IL-18 expression. Molecular docking confirmed that seven representative compounds of XQLD had good binding properties with NLRP3 and were able to inhibit the activation of the NLRP3 inflammasome. The representative compounds of XQLD might inhibit pyroptosis in nasal mucosa mediated by the NLRP3 inflammasome to helping the recovery of AR, which provides a new modern pharmacological proof for XQLD to treat AR.