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本文引用的文献

1
Controlled elevation of intraocular pressure in anesthetized mice.在麻醉小鼠中控制眼内压升高。
Exp Eye Res. 2024 Nov;248:110106. doi: 10.1016/j.exer.2024.110106. Epub 2024 Sep 20.
2
Effect of Ambient Lighting on Intraocular Pressure Rhythms in Rats.环境光照对大鼠眼压节律的影响。
Invest Ophthalmol Vis Sci. 2024 Aug 1;65(10):16. doi: 10.1167/iovs.65.10.16.
3
Profiling IOP-Responsive Genes in the Trabecular Meshwork and Optic Nerve Head in a Rat Model of Controlled Elevation of Intraocular Pressure.在眼压控制性升高的大鼠模型中对小梁网和视神经头部的眼压反应性基因进行分析。
Invest Ophthalmol Vis Sci. 2024 May 1;65(5):41. doi: 10.1167/iovs.65.5.41.
4
Optic Nerve Head Gene Transcription Sequelae to a Single Elevated IOP Exposure Provides Insights Into Known Responses to Chronically Elevated IOP.单一升高的眼内压暴露对视神经头基因转录的后续影响为深入了解已知的慢性升高的眼内压反应提供了线索。
Invest Ophthalmol Vis Sci. 2023 Jul 3;64(10):4. doi: 10.1167/iovs.64.10.4.
5
Vitrectomy using 0.025% povidone-iodine irrigation for treating post-traumatic endophthalmitis due to intraocular foreign bodies: Two case reports.使用0.025%聚维酮碘冲洗进行玻璃体切除术治疗眼内异物所致创伤后眼内炎:两例病例报告。
Front Surg. 2023 Jan 20;9:988776. doi: 10.3389/fsurg.2022.988776. eCollection 2022.
6
A method describing the microdissection of trabecular meshwork tissue from Brown Norway rat eyes.描述从褐家鼠眼睛中分离小梁网组织的显微解剖方法。
Exp Eye Res. 2023 Mar;228:109367. doi: 10.1016/j.exer.2022.109367. Epub 2023 Feb 3.
7
The Effect of Aging on Retinal Function and Retinal Ganglion Cell Morphology Following Intraocular Pressure Elevation.眼压升高后衰老对视网膜功能和视网膜神经节细胞形态的影响。
Front Aging Neurosci. 2022 May 12;14:859265. doi: 10.3389/fnagi.2022.859265. eCollection 2022.
8
Age and intraocular pressure in murine experimental glaucoma.鼠实验性青光眼的年龄与眼内压。
Prog Retin Eye Res. 2022 May;88:101021. doi: 10.1016/j.preteyeres.2021.101021. Epub 2021 Nov 18.
9
Intraocular Povidone Iodine During Pars Plana Vitrectomy for Severe and Atypical Endophthalmitis.严重非典型眼内炎行玻璃体切除术中应用聚维酮碘眼内冲洗。
Ophthalmic Surg Lasers Imaging Retina. 2021 Sep;52(9):485-490. doi: 10.3928/23258160-20210820-01. Epub 2021 Sep 1.
10
Sub-region-Specific Optic Nerve Head Glial Activation in Glaucoma.青光眼的亚区视神经头部神经胶质激活。
Mol Neurobiol. 2020 Jun;57(6):2620-2638. doi: 10.1007/s12035-020-01910-9. Epub 2020 Apr 7.

一种用于在清醒的棕色挪威大鼠中产生可控眼压升高的系统。

A system for producing controlled elevation of intraocular pressure in awake Brown Norway rats.

作者信息

Morrison John C, Cepurna William, Ing Eliesa, Johnson Elaine, Abtin Aryana, Wentzien Susan, White Elizabeth, Lozano Diana C

机构信息

Casey Eye Institute, Oregon Health & Science University, United States.

Casey Eye Institute, Oregon Health & Science University, United States.

出版信息

Exp Eye Res. 2025 Feb;251:110237. doi: 10.1016/j.exer.2025.110237. Epub 2025 Jan 11.

DOI:10.1016/j.exer.2025.110237
PMID:39805385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11824874/
Abstract

Animal models that help us understand how elevated intraocular pressure (IOP) causes axonal injury will lead to new glaucoma therapies. Because reliable measurements are difficult to obtain in chronic models, we developed the controlled elevation of IOP (CEI) approach. Here, a cannula connected to an elevated balanced salt solution (BSS) reservoir is inserted into the anterior chamber of anesthetized Brown Norway rats. The extent and duration of IOP exposure is controlled by adjusting the reservoir height. We now describe a method for creating CEI in awake animals. A Pinport, which has a silicone plug that can be penetrated repeatedly, is modified, attached to the skull, and connected to a microcannula that is implanted in the posterior chamber. To elevate IOP, BSS from a reservoir is allowed to flow through a pressure transducer to a swivel-mounted tether and injector. The injector is placed on the Pinport, bypassing the need for anterior chamber cannulation and general anesthesia during CEI. The surgical technique and equipment required for implantation are described, as well as the equipment and methods for performing awake CEI in several animals at a time. The ability of this system to control the level of IOP is demonstrated by TonoLab measurement, and by comparing reservoir (Pinport) pressures to direct measurement using an independent anterior chamber cannula and transducer. We also demonstrate that IOP elevation can be maintained over several hours. Specific pitfalls during and after surgical implantation are highlighted to help other researchers adopt these techniques.

摘要

有助于我们理解眼内压(IOP)升高如何导致轴突损伤的动物模型将带来新的青光眼治疗方法。由于在慢性模型中难以获得可靠的测量结果,我们开发了眼内压控制升高(CEI)方法。在此方法中,将连接到升高的平衡盐溶液(BSS)储液器的套管插入麻醉的挪威棕色大鼠的前房。通过调节储液器高度来控制眼内压暴露的程度和持续时间。我们现在描述一种在清醒动物中创建CEI的方法。对具有可重复穿透的硅胶塞的Pinport进行改装,将其连接到颅骨,并连接到植入后房的微套管。为了升高眼内压,使来自储液器的BSS流经压力传感器,再流到旋转安装的系绳和注射器。将注射器放置在Pinport上,从而在CEI过程中无需进行前房插管和全身麻醉。描述了植入所需的手术技术和设备,以及一次在几只动物中进行清醒CEI的设备和方法。通过TonoLab测量,并通过将储液器(Pinport)压力与使用独立的前房套管和传感器进行的直接测量进行比较,证明了该系统控制眼内压水平的能力。我们还证明眼内压升高可以维持数小时。强调了手术植入过程中和植入后的特定陷阱,以帮助其他研究人员采用这些技术。

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