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Updated: Jun 27, 2025

Induction of Ocular Surface Inflammation and Collection of Involved Tissues
Published on: August 4, 2022
Biochanin A: Disrupting the inflammatory vicious cycle for dry eye disease
Taige Chen1, Nan Zhou2, Qi Liang3
1Department of Ophthalmology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, 321 Zhongshan Road, Nanjing 210009, Jiangsu, China; Department of Rheumatology and Immunology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, 321 Zhongshan Road, Nanjing 210009, Jiangsu, China.
Abstract:
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.
Insights
Biochanin A (BCA) shows promise for treating dry eye disease (DED). This study found BCA eye drops reduced ocular inflammation and oxidative stress in a DED mouse model, suggesting a new therapeutic avenue.
Area of Science:
- Ophthalmology
- Pharmacology
- Cell Biology
Background:
- Dry eye disease (DED) is a multifactorial condition exacerbated by oxidative stress and inflammation.
- Antioxidants are explored for DED treatment due to the link between oxidative damage and ocular inflammation.
- Biochanin A (BCA), a red clover bioisoflavone, exhibits significant anti-inflammatory properties.
Purpose of the Study:
- To investigate the therapeutic potential of Biochanin A (BCA) for treating dry eye disease (DED).
- To evaluate BCA's effects on oxidative stress and ocular surface inflammation in preclinical models.
Main Methods:
- Human corneal epithelial cells were cultured under hyperosmotic conditions to simulate DED.
- A DED mouse model was established using low humidity and scopolamine injections.
- Mice received BCA eye drops, and outcomes included tear volume, corneal staining, inflammation markers, and Nrf2 pathway activation.
Main Results:
- BCA treatment improved corneal epithelial cell viability and reduced apoptosis and inflammatory cytokine expression in vitro.
- In vivo, BCA eye drops significantly reduced DED symptoms, including inflammation and oxidative stress markers.
- BCA enhanced the nuclear translocation of Nrf2, indicating activation of antioxidant pathways.
Conclusions:
- Biochanin A (BCA) effectively ameliorates oxidative stress and ocular surface inflammation in DED models.
- BCA demonstrates potential as a novel therapeutic agent for dry eye disease by mitigating oxidative damage and inflammation.
- Further research into BCA for DED treatment is warranted based on these promising preclinical findings.
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