Graduate Program in Biochemistry and Molecular Biology, Loyola University Chicago, Maywood, Illinois, USA.
Visual Neurobiology and Signal Transduction Laboratory, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA.
J Ocul Pharmacol Ther. 2022 May;38(4):294-304. doi: 10.1089/jop.2021.0131. Epub 2022 Apr 4.
Particulate matter (PM) is a primary cause for the development of acute and chronic dry eye disease, especially irritant-induced conjunctivitis. The purpose of the present study was to determine the effects of fine atmospheric PM on the rabbit ocular surface, and determine the protective effects of a synthetic antioxidant, manganese(III) tetrakis(1-methyl-4-pyridyl) porphyrin (Mn-TM-2-PyP), and . Rabbit corneal epithelial cells (SIRC) were exposed to increasing concentrations of PM to determine the effects on cell motility and viability. The effects of topically instilled PM were tested in New Zealand White rabbits. Comprehensive ophthalmic exams and corneal fluorescein staining were performed. Exposure to PM resulted in dose-dependent cell death and impaired cellular motility; Mn-TM-2-PyP protected against PM-induced cytotoxicity and significantly increased SIRC cell motility. , exposure to PM (5 mg/ml, topical, 3 times daily for 7 days) resulted in signs of dry eye, notably hyperemia, increased corneal fluorescein staining, and decreased tear volumes. Mn-TM-2-PyP significantly improved hyperemia and corneal fluorescein readouts but had no effect on tear production. Lifitegrast (Xiidra) showed similar pharmacologic efficacy to Mn-TM-2-PyP. Overall, these data provide evidence that PM induces phenotypes of ocular surface disease responsive to antioxidant and immunosuppressant therapy. To our knowledge this is the first report of a large animal model to study PM-induced ocular surface disease. The present work provides standardized experimental paradigms for the comprehensive and testing of novel therapeutic approaches targeting PM-induced conjunctivitis and dry-eye.
颗粒物 (PM) 是导致急性和慢性干眼症发展的主要原因,尤其是刺激性结膜炎。本研究旨在确定细颗粒大气 PM 对兔眼表面的影响,并确定一种合成抗氧化剂,锰 (III) 四 (1-甲基-4-吡啶基) 卟啉 (Mn-TM-2-PyP) 和 的保护作用。 用不同浓度的 PM 暴露兔角膜上皮细胞 (SIRC),以确定其对细胞迁移和活力的影响。在新西兰白兔中测试了局部滴注 PM 的影响。进行全面的眼科检查和角膜荧光素染色。 结果表明,PM 暴露导致剂量依赖性细胞死亡和细胞迁移受损;Mn-TM-2-PyP 可预防 PM 诱导的细胞毒性,并显著增加 SIRC 细胞迁移。 ,暴露于 PM(5mg/ml,局部,每日 3 次,共 7 天)导致干眼症的迹象,特别是充血、角膜荧光素染色增加和泪液量减少。Mn-TM-2-PyP 显著改善充血和角膜荧光素读数,但对泪液产生没有影响。利福昔明(Xiidra)显示出与 Mn-TM-2-PyP 相似的药理疗效。 总之,这些数据提供了证据表明 PM 诱导的眼表疾病表型对抗氧化剂和免疫抑制剂治疗有反应。据我们所知,这是第一个研究 PM 诱导的眼表疾病的大型动物模型的报告。本工作为针对 PM 诱导的结膜炎和干眼症的新型治疗方法的全面和测试提供了标准化的实验范例。