Tsai James C
Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York Eye and Ear Infirmary of Mount Sinai, New York, NY, USA.
J Ophthalmol. 2020 Apr 10;2020:9329310. doi: 10.1155/2020/9329310. eCollection 2020.
While sustained reduction of intraocular pressure (IOP) has been shown to halt and/or delay the progressive death of retinal ganglion cells (RGCs) in glaucoma, there exists great interest in the development and validation of IOP-independent therapeutic strategies for neuroprotection and/or neuroregeneration. Multiple etiologies for RGC death have been implicated in glaucoma including defective axonal transport, ischemia, excitotoxicity, reactive oxygen species, trophic factor withdrawal, and loss of RGC electrical activity. However, IOP lowering with medical, laser, and surgical therapies is itself neuroprotective, and investigators are seeking to identify agents that are able to confer neuroprotection independent of IOP reduction, as well as providing for regeneration of nonviable RGCs and their axons to restore and/or maintain functional vision. These innovative strategies in the pipeline include investigation of neurotrophic factors, gene therapy, immune system modulation, and novel neuroregeneration pathways. Alongside this new knowledge, enhanced opportunities for discovery of vision preservation and/or restoration therapies must be weighed against the potential disadvantages of perturbing the complex central nervous system environment.
虽然降低眼压(IOP)已被证明可阻止和/或延缓青光眼患者视网膜神经节细胞(RGC)的进行性死亡,但人们对开发和验证与眼压无关的神经保护和/或神经再生治疗策略有着浓厚兴趣。RGC死亡的多种病因与青光眼有关,包括轴突运输缺陷、缺血、兴奋性毒性、活性氧、营养因子缺乏以及RGC电活动丧失。然而,药物、激光和手术治疗降低眼压本身就具有神经保护作用,研究人员正在寻找能够在不降低眼压的情况下提供神经保护的药物,以及促使无活力的RGC及其轴突再生以恢复和/或维持功能性视力的药物。正在研究的这些创新策略包括对神经营养因子、基因治疗、免疫系统调节和新型神经再生途径的研究。伴随着这些新知识,在权衡发现视力保护和/或恢复疗法的更多机会时,必须考虑到干扰复杂的中枢神经系统环境可能带来的不利影响。