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DOI 10.1016/j.ejphar.2023.175607

Медицинская библиотека · European journal of pharmacology · 2023

Pentoxifylline treats Aspergillus fumigatus keratitis by reducing fungal burden and suppressing corneal inflammation.

Chi Menghui, Gu Lingwen, Zhang Lina, Lin Jing, Xu Qiang, Jiang Nan, Wang Yuwei, Qi Yinghe, Diao Weilin, Yi Wendan, Zhao Guiqiu, Li Cui

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Аннотация

Fungal keratitis (FK) is a blinding ocular disease, which mainly results from fungal damage and excessive inflammation. Pentoxifylline, a kind of methylxanthine, has been discovered to have anti-inflammatory properties in various infectious diseases, hinting a potential therapeutic effect on treating corneal fungal infection. Whereas, the therapeutic impact of pentoxifylline on fungal keratitis is still uncertain. This study investigated the antifungal capability against Aspergillus fumigatus and the anti-inflammatory role of pentoxifylline by activating nuclear factor, erythroid 2 like 2 (Nrf2)/heme oxygenase1 (HO1) pathway in the process of FK. In our research, we demonstrated that pentoxifylline could effectively inhibit fungal growth and inflammatory reaction. Pentoxifylline reduced the production of pro-inflammatory factors by stimulating the Nrf2/HO1 pathway. Although there was no statistical difference between the curative efficacy of pentoxifylline and natamycin application to FK, pentoxifylline could promote corneal epithelial repair and was less toxicity to the ocular surface than natamycin. In conclusion, pentoxifylline performs antifungal and anti-inflammatory effects by lessening the fungus burden and activating the Nrf2/HO1 pathway, hinting that it has the potential to be a new therapeutic medication for Aspergillus fumigatus keratitis.

Для цитирования: Chi Menghui, Gu Lingwen, Zhang Lina, Lin Jing, Xu Qiang, Jiang Nan, Wang Yuwei, Qi Yinghe, Diao Weilin, Yi Wendan, Zhao Guiqiu, Li Cui. Pentoxifylline treats Aspergillus fumigatus keratitis by reducing fungal burden and suppressing corneal inflammation.. European journal of pharmacology. 2023. DOI: 10.1016/j.ejphar.2023.175607.

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