高眼内压诱导视网膜缺血和光诱导视网膜病变的大鼠模型

Sze-Min Chan, Chung-Tien Lin
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引用次数: 0

摘要

青光眼和视网膜变性是两种重要的眼科疾病,通常会对人类和动物的视力造成严重影响。大鼠模型常用于探索这些疾病的复杂病理生理学和潜在治疗方法。高眼内压(HIOP)诱导的视网膜缺血再灌注模型意味着缺血结果重于视网膜内层(包括神经纤维层、视网膜神经节细胞(RGC)层、内丛状层(IPL)和视网膜内层(INL)),并最终发展到视网膜外层。根据缺血治疗的持续时间(周期),更多的青光眼病理变化征象可能会随着时间的推移而表现得更加明显。该模型需要较短的缺血治疗时间,并预计有足够长的疾病表现期。为了研究光感受器导致的视网膜变性,通常使用光诱导视网膜病变大鼠模型,其主要原因是高强度的光照射导致视网膜上层(ONL)和视网膜下层(OPL)的光感受器细胞受损。该模型揭示了光传导的病理生理损伤以及涉及氧化应激和视网膜外层炎症过程的疾病机制。通过对这些动物模型的研究,可以更好地了解病理生理学和分子变化方面的疾病机制。此外,大鼠模型还可作为进一步研究这些视网膜病变的治疗或预防前景的重要依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIGH INTRAOCULAR PRESSURE-INDUCED RETINAL ISCHEMIA AND LIGHT-INDUCED RETINOPATHY IN RAT MODELS
Glaucoma and retinal degenerations are two important ocular diseases that often cause massive impacts to vision in both humans and animals. Rat models are commonly used to explore the complex pathophysiology and potential treatments of these diseases. The models of high intraocular pressure (HIOP)-induced retinal ischemia-reperfusion imply the ischemic outcome weight on the inner retina layers (including the nerve fiber layer, retinal ganglion cell (RGC) layer, inner plexiform layer (IPL), and inner retinal layer (INL)) that eventually progressed to the outer retinal layers. Depending on the duration (cycles) of ischemic treatment, more glaucoma pathological change signs may be exhibited more obviously with time. The model requires a short ischemic treatment and anticipates an adequately long period of disease manifestation. To investigate photoreceptor-led retinal degeneration, rat models for light-induced retinopathy are commonly used and it is predominantly attributed to the photoreceptor cells damage of ONL and OPL loss by high intensity of light exposure. This model unraveled the pathophysiological impairment of phototransduction as well as disease mechanisms involving oxidative stress and inflammatory process of the outer retinal layer. With the knowledge gained from the research using these animal models, better understanding of the disease mechanisms in terms of its pathophysiology and molecular changes can be achieved. Besides, the rat models can serve as the key basis for further investigation into the therapeutic or preventive perspectives of these retinopathies.
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