岩藻黄素在实验性青光眼中保护视网膜神经节细胞并调节帕金森介导的有丝分裂。

IF 2.2 Q2 OPHTHALMOLOGY
Haixia Ma, Xinxin Hu, Juntao Zhang, Wei Lian, Dandan Wang, Lifang Zhang, Qinkang Lu
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引用次数: 0

摘要

目的:青光眼是一种常见的导致不可逆失明的神经退行性疾病。本研究探讨岩藻黄素是否通过调节帕金森蛋白介导的线粒体自噬来保护实验性青光眼视网膜神经节细胞(rgc)。方法:采用经角膜激光光凝法制备Sprague-Dawley大鼠青光眼模型。使用Tonolab眼压计监测眼压。通过fluorgold标记评估RGC生存期。在iop升高后3天和2周,使用免疫组织化学和分子分析视网膜和视神经样本的线粒体形态和基因/蛋白表达。结果:高眼压大鼠有丝分裂在短期内急性过度激活,在长期内受损。岩藻黄素玻璃体内注射可提高RGC存活率和Bcl-2表达,同时降低Bax和胶质纤维酸性蛋白水平。在急性IOP升高期间,岩藻黄素抑制Parkin的表达和丝裂体的形成,减轻过度的丝裂体。在长时间IOP升高下,线粒体自噬相关蛋白升高,线粒体自噬功能恢复,导致线粒体清除受损。结论:岩藻黄素通过调节帕金森氏蛋白介导的线粒体自噬,对实验性青光眼具有神经保护作用。这突出了维持线粒体自噬稳态对青光眼治疗的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fucoxanthin protects retinal ganglion cells and regulates Parkin-mediated mitophagy in experimental glaucoma.

Objective: Glaucoma is a common neurodegenerative disease resulting in irreversible blindness. This study investigates whether fucoxanthin can safeguard retinal ganglion cells (RGCs) by modulating Parkin-mediated mitophagy in experimental glaucoma.

Methods: An experimental glaucomatous model was induced in Sprague-Dawley rats via translimbal laser photocoagulation. Intraocular pressure (IOP) was monitored using a Tonolab tonometer. RGC survival was evaluated through FluoroGold labelling. Retinal and optic nerve samples were analysed at 3 days and 2 weeks post-IOP elevation for mitochondrial morphology and gene/protein expression using immunohistochemistry and molecular assays.

Results: Results demonstrated that mitophagy was acutely overactivated in the short term and impaired over the long term in ocular hypertensive rats. Fucoxanthin intravitreal administration enhanced RGC survival and Bcl-2 expression while reducing Bax and glial fibrillar acidic protein levels. During acute IOP elevation, fucoxanthin curtailed Parkin expression and mitophagosome formation, mitigating excessive mitophagy. Under prolonged IOP elevation, it elevated mitophagy-related proteins and restored mitophagy function, contributing to damaged mitochondrial clearance.

Conclusion: Fucoxanthin exerts neuroprotective effects in experimental glaucoma by modulating Parkin-mediated mitophagy. This highlights the therapeutic potential of maintaining mitophagy homeostasis for glaucoma treatment.

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来源期刊
BMJ Open Ophthalmology
BMJ Open Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
4.20%
发文量
104
审稿时长
20 weeks
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