Abstract
BACKGROUND: Atopic dermatitis (AD) is a chronic, recurrent inflammatory skin disorder that causes systemic skin lesions. The hospital preparation-Qinzhuliangxue mixture (QZLX) has shown potential in alleviating skin lesions in AD patients; however, its underlying mechanisms remain largely unexplored. METHODS: QZLX's key compounds and their targets in AD skin lesions were screened by network pharmacology, and gene enrichment analysis was performed. Mouse model of AD induced by 2,4-dinitrofluorobenzene (DNFB) was established. Then animals were divided into control (Con), model (Model), dexamethasone (DSMS), and QZLX group. The DSMS group and QZLX group was orally administrated DSMS (10 mg/kg/day) and QZLX (18.27 g/kg/day) for 14 days respectively, after the DNFB was first injected intradermally into the abdomen of mice. Phenotypic changes in mice after treatment were evaluated by skin SCORAD score, hematoxylin-eosin (HE) staining, ELISA assays, and Western Blot (WB). RESULTS: According to the findings of enrichment analysis based on GO and KEGG, QZLX may exert its effects at the top position via the JAK-STAT pathway. Subsequently the experimental validation showed that the skin score and HE staining of the QZLX group was significantly improved compared to the Model group (P < 0.05). Moreover, the levels of serum IgE, TSLP, and IL-4 in the QZLX group were notably lower than those in the Model group (P < 0.05). Furthermore, the expression of P-JAK2 and P-STAT3 detected by WB in the skin of the QZLX group was obviously higher than that in the Model group (P < 0.05). CONCLUSION: QZLX demonstrated a significant ability to mitigate AD-like skin lesions and effectively reduced serum levels of IgE, TSLP, and IL-4 in AD mice. The underlying mechanism of action may involve modulation via the JAK2/STAT3 pathway.