期刊文献+

大鼠慢性高眼压青光眼模型的构建及鉴定

Construction and appraisal of chronic ocular hypertension glaucoma model of rats
下载PDF
导出
摘要 目的:手术建立慢性高眼压青光眼大鼠模型对研究青光眼发病机制、治疗和视神经保护这三方面的研究尤为必要。方法:烧灼3条表浅巩膜静脉,并术中联合应用结膜瓣下浸有0.2g/L的丝裂霉素的凝胶海绵,阻断大鼠的眼部房水外流,建立大鼠慢性高眼压模型,手术后2h;1,3,7,14,28,56d处死5只大鼠,空白对照组亦处死5只大鼠;摘除眼球光镜下进行视网膜形态的观察及视网膜厚度测量,研究眼压、视网膜神经节细胞(retinal ganglion cells,RGC)和视神经损伤的特性。结果:大鼠手术眼与假手术眼、空白对照眼的术后各时间点的眼压比较差异有显著性(P<0.01)。结论:建立大鼠慢性高眼压模型操作简单,重复性好,成模率高,高眼压可稳定维持长时间,慢性高眼压将导致整个视网膜的变薄和萎缩。 AIM: The establishment of chronic ocular hypertension surgery glaucoma animal model for the study of the pathogenesis, treatment and protection of these three aspects of the optic nerve is particularly necessary. METHODS: Superficial burning three episcleral veins, and surgery combined with conjunctival flap under the Baptist has the mitomycin C 0.2g/L gel sponge , to block rat aqueous outflow of the eye can induce by intraocular pressure(lOP), the establishment of rat model of chronic high intraocular pressure. After surgery 2 hours, 1 day, 3, 7, 14, 28, 56 days, 5 rats were killed, blank control group, also killed 5 rats; Eyeballs were removed for light microscopy, retinal eye patterns observation and measurement of retinal thickness in order to study the lOP, retinal ganglion cells(RGC) and optic nerve injury characteristics. RESULTS: The rats with sham surgery eye eyes, eye control of postoperative intraocular pressure at different time points of comparison there was a significant difference ( P〈 0.01 ). CONCLUSION: Rats with chronic ocular hypertension model is simple, reproducible and high rate into a mold, high intraocular pressure may maintain stability for a longtime. Chronic high intraocular pressure of the final results will lead to the thinning of the retina and atrophy.
出处 《国际眼科杂志》 CAS 2009年第8期1463-1465,共3页 International Eye Science
基金 中国辽宁省科技厅攻关计划项目(No.20040380)角膜缘基质微环境诱导脐血干细胞分化研究~~
关键词 慢性高眼压 青光眼 视网膜神经节细胞 大鼠 chronic high intraocular pressure glaucoma retinal ganglion cells rat
  • 相关文献

参考文献8

  • 1Medzhitov R, Janeway C Jr. Innate immune recognition: mechanisms and path ways. Immunology 2000 ; 173 : 89-97.
  • 2Mermoud A, Baerveldt G, Mickler DS, et al. Animal model for uveitic glaucoma. Graefes Arch Clin Exp Ophthalmol 1994 ;232(9 ) :553-560.
  • 3Shareef SR, Garcia-Valenzuela E, Saliemo A, et al . Chronic ocular hypertension following episcleral venousoeclusion in rats. Exp Eye Res 1995 ;61 (3) :379-382.
  • 4Morrison J C, Moore Pmeier LMH. A rat model fehronie pressure-induced opitic never damage. Exp Eye Res 1997;64( 1 ) :85-96.
  • 5Ued J, Sawaguehi S, Hanyu T, et al. Experimental glaucoma model in the rat Induced by laser trabecular Photoeoa gulation after an intracameral in jeetion of India ink.Jpn J Ophthalmol 1998 ;42(4) :337-344.
  • 6Levkovitch Verbin H, Quigley HA, Martin KRG, et al. Translimbal laser hotocoagulation to the trabecular meshwork model of glaucoma in rats. Invest Ophthalmol Vis Sci 2002 ;43 ( 2 ) :402-410.
  • 7Wang RF, Schumer RA, Serle JB, et al. A comparison of argon-laser and diode laser photocoagulation of the trabecular meshwork to produce the glaucoma monkey model.J Glaucoma 1998 ;7 (1) :45-49.
  • 8Mittag TW, Danias J, Pohorenee G, et al. Retinal Damage after 3 to 4 Months Elevated Intraocular Pressure in a Rat Glaucoma Model. Invest Ophthalmol Vis Sci 2000 ;41 ( 11 ) :3451-3459.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部