Berberine ameliorate inflammation and apoptosis via modulating PI3K/AKT/NFκB and MAPK pathway on dry eye

细胞凋亡 蛋白激酶B PI3K/AKT/mTOR通路 MAPK/ERK通路 药理学 活力测定 炎症 化学 体内 小檗碱 医学 信号转导 生物 免疫学 生物化学 生物技术
作者
Yi Han,Shujia Guo,Yunpeng Li,Jiani Li,Linfangzi Zhu,Yuwen Liu,Yufei Lv,Yu Dong,Lan Zheng,Caihong Huang,Cheng Li,Jiaoyue Hu,Lei Zhu
出处
期刊:Phytomedicine [Elsevier]
卷期号:121: 155081-155081 被引量:13
标识
DOI:10.1016/j.phymed.2023.155081
摘要

Dry eye disease (DED) is a multifactorial disease in ocular surface, and inflammation plays an etiological role. Berberine (BBR) has shown efficacy in treating inflammatory diseases. Yet, there was no adequate information related to the therapeutic effects of BBR for DED.To detect the effects and explore the potential mechanisms of BBR on DED.In vitro, in vivo study and network pharmacology analysis were involved.The human corneal epithelium cells viability was evaluated with different concentrations of BBR. Dry eye murine model was established by exposing to the desiccating stress, and Ciclosporin (CSA), BBR eye drops or vehicle were topical administration for 7 days. The phenol red cotton tests, Oregon-green-dextran staining and Periodic acid-Schiff staining were performed and evaluated the dry eye after treatment. Inflammation and apoptosis levels of ocular surface were quantified. The potential targets related to berberine and dry eye were collected from databases. The Protein-Protein interaction network analysis and GO & KEGG enrichment analysis were realized by STRING database, Metascape platform and Cytoscape software to find core targets and signaling pathways. The SchrÖdinger software was used to molecular docking and PyMOL software to visualization. Finally, the levels of PI3K/AKT/NFκB and MAPK pathways were detected.The data revealed BBR could rescue impaired HCE under hyperosmotic conditions. In addition, BBR eye drops could ameliorate dry eye. And BBR eye drops suppressed the inflammatory factors and CD4+T cells infiltration in conjunctiva. Besides, BBR eye drops protected ocular surface by avoiding the severe apoptosis and decreasing the level of MMP-3 and MMP-9. 148 common targets intersection between BBR and dry eye were found via network pharmacology analysis. Core proteins and core pathways were identified through PPI and GO&KEGG enrichment analysis. Molecular docking displayed excellent binding between BBR and those core targets. Finally, in vivo study verified that BBR eye drops had a therapeutic effect in dry eye by inhibiting PI3K/AKT/NFκB and MAPK pathways.The research provided convincing evidence that BBR could be a candidate drug for dry eye.
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