Jing Zhang1, Yiqin Dai1, Dan Wu1, Jianjiang Xu1. 1. a Department of Ophthalmology and Visual Science , Eye & ENT Hospital of Fudan University, Key Laboratory of Myopia, Ministry of Health , Shanghai , China.
Abstract
PURPOSE: To examine the influence of topical administration of calcitriol on dry eye (DE) related corneal inflammation. METHODS: Benzalkonium chloride (BAC, 0.2%) was applied to induce DE. Then rats were treated topically with calcitriol (10-6μM). Tear break-up time (TBUT), fluorescein staining score, inflammatory index, and tear volume were measured. Corneal epithelium damage and corneal inflammation were examined by H&E staining or RT-qPCR. In vitro, human corneal epithelial cells (iHCEC) were cultured in hyperosmotic medium (450 mOsM) with various concentrations of calcitriol. Levels of pro-inflammatory mediators were measured by RT-qPCR or ELISA. NF-κB activation was examined by Western blotting and immunofluorescence staining. RESULTS: Calcitriol significantly ameliorated DE symptoms, attenuating corneal inflammation. In vitro studies showed that calcitriol significantly decreased the expression of pro-inflammatory mediators in iHCECs under hyperosmotic stress, probably through inhibiting NF-κB activation. CONCLUSION: The results suggest that calcitriol might be a potential therapeutic agent for DE.
PURPOSE: To examine the influence of topical administration of calcitriol on dry eye (DE) related corneal inflammation. METHODS:Benzalkonium chloride (BAC, 0.2%) was applied to induce DE. Then rats were treated topically with calcitriol (10-6μM). Tear break-up time (TBUT), fluorescein staining score, inflammatory index, and tear volume were measured. Corneal epithelium damage and corneal inflammation were examined by H&E staining or RT-qPCR. In vitro, human corneal epithelial cells (iHCEC) were cultured in hyperosmotic medium (450 mOsM) with various concentrations of calcitriol. Levels of pro-inflammatory mediators were measured by RT-qPCR or ELISA. NF-κB activation was examined by Western blotting and immunofluorescence staining. RESULTS:Calcitriol significantly ameliorated DE symptoms, attenuating corneal inflammation. In vitro studies showed that calcitriol significantly decreased the expression of pro-inflammatory mediators in iHCECs under hyperosmotic stress, probably through inhibiting NF-κB activation. CONCLUSION: The results suggest that calcitriol might be a potential therapeutic agent for DE.
Entities:
Keywords:
Calcitriol; DE; corneal inflammation; vitamin D