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经瞳孔温热激光视神经头部辐照对视神经节细胞的神经保护作用。

Neuroprotective effect on retinal ganglion cells by transpupillary laser irradiation of the optic nerve head.

机构信息

Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, PR China.

出版信息

Neurosci Lett. 2010 May 26;476(1):3-8. doi: 10.1016/j.neulet.2010.01.001. Epub 2010 Jan 7.

Abstract

This study demonstrates that subthreshold transpupillary thermotherapy (TTT) laser irradiation on optic nerve head protects retinal ganglion cells (RGCs) in an optic nerve crush (ONC) model. TTT was performed in right eyes with an 810-nm diode laser aimed at the center of the optic nerve head, using the following protocol: power 60mW, duration 60s, spot size 500mum. Fluoro-Gold was injected into bilateral superior colliculi 5 days before sacrifice and fluorescent gold labeled RGCs were counted under fluorescence microscopy. In the ONC group, a progressive loss of RGCs was observed; however, in comparison with the ONC group, RGCs density was significantly higher (P=0.001, independent samples t-test) at day 7 postoperative and only borderline significances were obtained at days 14 and 28 postoperative (P=0.044 and P=0.045, respectively, independent samples t-test) in ONC+TTT group, which implies the potential neuroprotective role of TTT. This protective effect seems to be heat shock proteins (HSPs) related, because intraperitoneal Quercetin (an inhibitor of HSPs, 4mg/kg/day for 7 days) could completely abolish this protective effect at days 7, 14 and 28 postoperative (P=0.012, P=0.002, and P=0.000, respectively, independent samples t-test). Minimal collateral damage of TTT on optic nerve head tissue, peripapillary RGCs and the myelin sheath of the optic nerve were observed under transmission electron microscopy. These findings suggested that subthreshold TTT might be a safe and practical approach to protect RGCs. The underlying mechanisms may involve TTT-induced HSPs in RGCs.

摘要

本研究表明,阈下经瞳孔温热疗法(TTT)激光辐照视神经头部可在视神经挤压(ONC)模型中保护视网膜神经节细胞(RGC)。在右眼用 810nm 二极管激光进行 TTT,激光瞄准视神经头部的中心,使用以下方案:功率 60mW,持续时间 60s,光斑大小 500mum。在牺牲前 5 天,将荧光金注入双侧上丘,并在荧光显微镜下计数荧光金标记的 RGC。在 ONC 组中,观察到 RGC 的进行性丧失;然而,与 ONC 组相比,ONC+TTT 组术后第 7 天的 RGC 密度显著更高(P=0.001,独立样本 t 检验),仅在术后第 14 天和第 28 天获得边缘显著(P=0.044 和 P=0.045,独立样本 t 检验),这意味着 TTT 具有潜在的神经保护作用。这种保护作用似乎与热休克蛋白(HSPs)有关,因为腹腔内 Quercetin(HSPs 的抑制剂,每天 4mg/kg,持续 7 天)可在术后第 7、14 和 28 天完全消除这种保护作用(P=0.012,P=0.002 和 P=0.000,独立样本 t 检验)。在透射电子显微镜下观察到 TTT 对视神经头部组织、视盘周围 RGC 和视神经髓鞘的最小的附带损伤。这些发现表明,阈下 TTT 可能是一种安全实用的方法来保护 RGC。潜在的机制可能涉及 TTT 诱导的 RGC 中的 HSPs。

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