阿魏酸
胸腺基质淋巴细胞生成素
特应性皮炎
哈卡特
细胞因子
发病机制
免疫学
药理学
医学
炎症
抗氧化剂
化学
肿瘤坏死因子α
免疫组织化学
白细胞介素
促炎细胞因子
生物化学
下调和上调
香豆酸
咖啡酸
趋化因子
氧化应激
作者
E. E. Akgun,B. Gulbenli Turkoglu
标识
DOI:10.15547/bjvm.2025-0125
摘要
Atopic dermatitis (AD) is a chronic inflammatory skin disease characterised by impaired skin bar-rier function and predominant Th2-mediated inflammation. Thymic stromal lymphopoietin (TSLP), a cytokine secreted by epidermal keratinocytes, plays a critical role in AD pathogenesis by initiating and amplifying allergic inflammation. Ferulic acid (FA), a natural phenolic compound with potent antioxidant and anti-inflammatory properties, has gained attention as a potential therapeutic agent for AD. This study evaluated the effects of ferulic acid on TSLP expression using immunohistochemical staining in an experimental AD model. Histopathological analysis revealed that ferulic acid treatment significantly reduced epidermal thickness and inflammatory cell infiltration, compared to 2,4-dinitrochlorobenzene (DNCB) group. Furthermore, TSLP immunoreactivity was markedly decreased following ferulic acid administration. In addition, real-time PCR analysis demonstrated that ferulic acid significantly downregulated the mRNA expression levels of pro-inflammatory cytokines TNF-α, IL-4, and IL-13. These findings suggest that ferulic acid modulates TSLP-mediated inflammatory responses and improves histopathological outcomes in AD, highlighting its potential as a supportive treatment option for atopic dermatitis.
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