Morrison John C, Johnson Elaine C, Cepurna William O
Casey Eye Institute, Oregon Health and Science University, 3375 S.W. Terwilliger Blvd, Portland, OR, 97239, USA.
Methods Mol Biol. 2018;1695:11-21. doi: 10.1007/978-1-4939-7407-8_2.
A reliable method of creating chronic elevation of intraocular pressure (IOP) in rodents is an important tool in reproducing and studying the mechanisms of optic nerve injury that occur in glaucoma. In addition, such a model could provide a valuable method for testing potential neuroprotective treatments. This paper outlines the basic methods for producing obstruction of aqueous humor outflow and IOP elevation by injecting hypertonic saline (a sclerosant) into the aqueous outflow pathway. This is one of several rodent glaucoma models in use today. In this method, a plastic ring is placed around the equator of the eye to restrict injected saline to the limbus. By inserting a small glass microneedle in an aqueous outflow vein in the episclera and injecting hypertonic saline toward the limbus, the saline is forced into Schlemm's canal and across the trabecular meshwork. The resultant inflammation and scarring of the anterior chamber angle occurs gradually, resulting in a rise in IOP after approximately 1 week. This article will describe the equipment necessary for producing this model and the steps of the technique itself.
在啮齿动物中建立可靠的眼内压(IOP)慢性升高方法,是再现和研究青光眼视神经损伤机制的重要工具。此外,这种模型可为测试潜在的神经保护治疗提供有价值的方法。本文概述了通过向房水流出途径注射高渗盐水(一种硬化剂)来产生房水流出阻塞和IOP升高的基本方法。这是目前使用的几种啮齿动物青光眼模型之一。在该方法中,将一个塑料环放置在眼球赤道周围,以将注入的盐水限制在角膜缘。通过将一根小玻璃微针插入巩膜上的房水流出静脉并向角膜缘注射高渗盐水,盐水被压入施莱姆管并穿过小梁网。前房角由此产生的炎症和瘢痕形成会逐渐发生,大约1周后导致IOP升高。本文将描述建立该模型所需的设备以及该技术本身的步骤。