Biochanin A: Disrupting the inflammatory vicious cycle for dry eye disease

氧化应激 炎症 细胞凋亡 角膜上皮 免疫学 促炎细胞因子 活性氧 药理学 病理 医学 化学 内分泌学 上皮 生物化学
作者
Taige Chen,Nan Zhou,Qi Liang,Qi Li,Boda Li,Yiran Chu,Di Zhang,Zeying Chen,J. W. Tsao,Xuebing Feng,Kai Hu
出处
期刊:European Journal of Pharmacology [Elsevier BV]
卷期号:977: 176583-176583
标识
DOI:10.1016/j.ejphar.2024.176583
摘要

Dry eye disease (DED) is a complex disorder driven by several factors like reduced tear production, increased evaporation, or poor tear quality. Oxidative stress plays a key role by exacerbating the inflammatory cycle. Previous studies explored antioxidants for DED treatment due to the link between oxidative damage and inflammation. Biochanin A (BCA) is a bioisoflavone from red clover with potent anti-inflammatory effects. This study investigated BCA's therapeutic potential for DED. Human corneal epithelial cells were cultured under hyperosmotic conditions to mimic DED. BCA treatment increased cell viability and decreased apoptosis and inflammatory cytokine expression. A DED mouse model was developed using female C57BL/6 mice in a controlled low-humidity environment combined with scopolamine injections. Mice received eye drops containing phosphate-buffered saline, low-dose BCA, or high-dose BCA. The effectiveness was evaluated by measuring tear volume, fluorescein staining, eye-closing ratio, corneal sensitivity and PAS staining. The levels of inflammatory components in corneas and conjunctiva were measured to assess DED severity. Maturation of antigen-presenting cells in cervical lymph nodes was analyzed by flow cytometry. BCA eye drops effectively reduced inflammation associated with DED in mice. BCA also decreased oxidative stress levels by reducing reactive oxygen species and enhancing the nuclear translocation of nuclear factor erythroid-2-related factor 2 (Nrf2). These findings demonstrate that BCA ameliorates oxidative stress and ocular surface inflammation, indicating potential as a DED treatment by relieving oxidative damage and mitigating inflammation.
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