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青光眼的啮齿动物模型及其意义。

The Rodent Model of Glaucoma and Its Implications.

作者信息

Chen Shida, Zhang Xiulan

机构信息

From the Zhongshan Ophthalmic Center, State Key Laboratory of Ophthalmology, Sun Yat-sen University, Guangzhou, China.

出版信息

Asia Pac J Ophthalmol (Phila). 2015 Jul-Aug;4(4):236-41. doi: 10.1097/APO.0000000000000122.

DOI:10.1097/APO.0000000000000122
PMID:26147015
Abstract

Glaucoma is a group of progressive optic neuropathies, characterized by the degeneration of retinal ganglion cells related to the level of intraocular pressure and other factors. The exact pathogenesis of glaucoma is not known, and current therapeutic options are not sufficient to prevent or recover vision loss in glaucoma patients. Functional, repeatable, and easy-to-use animal models are therefore needed. Because of their inherent advantages, rodent animals, including mice and rats, have been widely developed as models to study various aspects of glaucoma and to evaluate possible novel therapies. However, no single model has been shown to emulate all aspects of glaucoma. In this review, we discuss currently available rodent animal models of glaucoma, their strengths and weaknesses, and the possible implications for current glaucoma research.

摘要

青光眼是一组进行性视神经病变,其特征是视网膜神经节细胞的退化与眼压水平及其他因素有关。青光眼的确切发病机制尚不清楚,目前的治疗方法不足以预防或恢复青光眼患者的视力丧失。因此,需要功能性、可重复且易于使用的动物模型。由于其固有的优势,包括小鼠和大鼠在内的啮齿动物已被广泛开发为研究青光眼各个方面和评估可能的新疗法的模型。然而,没有一个单一的模型能模拟青光眼的所有方面。在这篇综述中,我们讨论了目前可用的啮齿动物青光眼模型、它们的优缺点以及对当前青光眼研究的可能影响。

相似文献

1
The Rodent Model of Glaucoma and Its Implications.青光眼的啮齿动物模型及其意义。
Asia Pac J Ophthalmol (Phila). 2015 Jul-Aug;4(4):236-41. doi: 10.1097/APO.0000000000000122.
2
Understanding glaucomatous damage: anatomical and functional data from ocular hypertensive rodent retinas.了解青光眼损伤:高眼压症啮齿动物视网膜的解剖学和功能数据。
Prog Retin Eye Res. 2012 Jan;31(1):1-27. doi: 10.1016/j.preteyeres.2011.08.001. Epub 2011 Sep 21.
3
Effect of ocular hypertension on the pattern of retinal ganglion cell subtype loss in a mouse model of early-onset glaucoma.早期发病青光眼小鼠模型中眼高压对视神经节细胞亚型丢失模式的影响。
Exp Eye Res. 2019 Aug;185:107703. doi: 10.1016/j.exer.2019.107703. Epub 2019 Jun 15.
4
A rat experimental model of glaucoma incorporating rapid-onset elevation of intraocular pressure.一种包含眼内压快速升高的大鼠青光眼实验模型。
Sci Rep. 2014 Aug 1;4:5910. doi: 10.1038/srep05910.
5
Longitudinal evaluation of morphological, functional and vascular alterations in a rat model of experimental glaucoma.实验性青光眼大鼠模型中形态、功能和血管改变的纵向评估。
Vision Res. 2024 Oct;223:108458. doi: 10.1016/j.visres.2024.108458. Epub 2024 Jul 29.
6
[The use of mice in glaucoma research --to clarify the mechanism of intraocular pressure regulation and retinal ganglion cell damage].[小鼠在青光眼研究中的应用——阐明眼压调节机制和视网膜神经节细胞损伤]
Nippon Ganka Gakkai Zasshi. 2010 Mar;114(3):217-46; discussion 247.
7
Changes in the modulation of retinocollicular transmission through group III mGluRs long after an increase in intraocular pressure in a rat model of glaucoma.在青光眼大鼠模型中,眼内压升高很久之后,通过III组代谢型谷氨酸受体对视神经-丘脑传递调节的变化。
Vis Neurosci. 2012 Sep;29(4-5):237-46. doi: 10.1017/S0952523812000193. Epub 2012 May 30.
8
The Microbead Occlusion Model of Ocular Hypertension in Mice.小鼠高眼压微珠阻塞模型
Methods Mol Biol. 2018;1695:23-39. doi: 10.1007/978-1-4939-7407-8_3.
9
Systemic hypertension is not protective against chronic intraocular pressure elevation in a rodent model.系统性高血压不能预防啮齿动物模型中慢性眼压升高。
Sci Rep. 2018 May 8;8(1):7107. doi: 10.1038/s41598-018-25264-4.
10
Inducible rodent models of glaucoma.诱导性青光眼啮齿动物模型。
Prog Retin Eye Res. 2020 Mar;75:100799. doi: 10.1016/j.preteyeres.2019.100799. Epub 2019 Sep 23.

引用本文的文献

1
The role of neurotrophic factors in retinal ganglion cell resiliency.神经营养因子在视网膜神经节细胞弹性中的作用。
Front Cell Neurosci. 2025 Jan 29;19:1536452. doi: 10.3389/fncel.2025.1536452. eCollection 2025.
2
An inducible rodent glaucoma model that exhibits gradual sustained increase in intraocular pressure with distinct inner retina and optic nerve inflammation.一种可诱导的啮齿动物青光眼模型,其表现为眼内压逐渐持续升高,伴有明显的内视网膜和视神经炎症。
Sci Rep. 2021 Nov 24;11(1):22880. doi: 10.1038/s41598-021-02057-w.
3
Changes of Ocular Dimensions as a Marker of Disease Progression in a Murine Model of Pigmentary Glaucoma.
眼部尺寸变化作为色素性青光眼小鼠模型疾病进展的标志物
Front Pharmacol. 2020 Sep 4;11:573238. doi: 10.3389/fphar.2020.573238. eCollection 2020.
4
Peripheral Latanoprost Administration Lowers Intraocular Pressure in the Wistar Rat.局部应用拉坦前列素可降低Wistar大鼠的眼压。
Ophthalmol Ther. 2020 Sep;9(3):1-8. doi: 10.1007/s40123-020-00256-8. Epub 2020 Aug 5.
5
A Reversible Silicon Oil-Induced Ocular Hypertension Model in Mice.一种小鼠可逆性硅油诱导性高眼压模型。
J Vis Exp. 2019 Nov 15(153). doi: 10.3791/60409.
6
Effect of ocular hypertension on the pattern of retinal ganglion cell subtype loss in a mouse model of early-onset glaucoma.早期发病青光眼小鼠模型中眼高压对视神经节细胞亚型丢失模式的影响。
Exp Eye Res. 2019 Aug;185:107703. doi: 10.1016/j.exer.2019.107703. Epub 2019 Jun 15.
7
Silicone oil-induced ocular hypertension and glaucomatous neurodegeneration in mouse.硅酮油诱导的小鼠眼内高压和青光眼性神经退行性变。
Elife. 2019 May 15;8:e45881. doi: 10.7554/eLife.45881.
8
Laser Capture Microdissection of Highly Pure Trabecular Meshwork from Mouse Eyes for Gene Expression Analysis.用于基因表达分析的小鼠眼高纯度小梁网激光捕获显微切割术。
J Vis Exp. 2018 Jun 3(136):57576. doi: 10.3791/57576.
9
Ezh2 does not mediate retinal ganglion cell homeostasis or their susceptibility to injury.Ezh2并不介导视网膜神经节细胞的稳态或其对损伤的易感性。
PLoS One. 2018 Feb 6;13(2):e0191853. doi: 10.1371/journal.pone.0191853. eCollection 2018.