经角膜电刺激(TES)灵活刺激模式对青光眼小鼠模型的脑激活作用。

IF 3 2区 医学 Q1 OPHTHALMOLOGY
D. Gomez-Maldonado , R. Shovmer , D.M. Inman , R.K. Willits
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引用次数: 0

摘要

经角膜电刺激(TES)已被证明是治疗DBA/2J型青光眼模型小鼠视神经病变的一种有前景的治疗方法,然而目前关于最有效的应用参数(如强度和持续时间)的知识有限。在本研究中,在电生理评估和眼压测量后,对双眼进行单次TES治疗,并测量上丘c-Fos的表达作为反应。取4、8月龄小鼠,公母各2只,各组分别给予1、10、100 μA治疗10、30 min;以无刺激组作为阴性对照,以生理盐水溶液腹腔注射作为阳性对照。以3月龄小鼠为病理生理基线,比较注射后各组(阳性对照组)和未刺激组(阴性对照组)c-Fos的表达。与年轻的对照组相比,8个月大的小鼠表现出可测量的神经病变进展。在低至1 μA的TES作用30 min时,可以检测到活性c- fos标记的细胞,这表明TES的优势可以通过灵活的应用范例来利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain activation following flexible stimulation paradigms of transcorneal electrical stimulation (TES) in a murine model of glaucoma
Transcorneal electrical stimulation (TES) has been shown as a promising treatment for optic neuropathy in DBA/2J glaucoma model mice, however the current knowledge about the most effective application parameters, such as intensity and duration, is limited. In this study, after electrophysiological evaluation and intraocular pressure measurements, a single TES treatment in both eyes was performed and expression of c-Fos in the superior colliculus measured as a response. Groups were formed with 4, 8-month-old mice, 2 male and 2 female, and treated with 1, 10, or 100 μA for 10 or 30 min; a group with no stimulation was used as negative control, and as positive control, a group of mice were injected intraperitoneally with saline solution. As pathophysiology baseline, groups of 3-month-old mice were used to compare the c-Fos expression after injection (positive control), and with no stimulation (negative controls). The 8-month-old mice presented measurable progression of neuropathy compared to young controls. Active c-Fos-labeled cells were detected with TES application as low as 1 μA for 30 min, suggesting that benefits of TES can be harnessed with flexible application paradigms.
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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