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慢性眼压升高导致的视网膜神经节细胞功能障碍的可逆性。

Reversibility of Retinal Ganglion Cell Dysfunction From Chronic IOP Elevation.

机构信息

Department of Optometry and Vision Sciences, University of Melbourne, Parkville, Victoria, Australia.

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Invest Ophthalmol Vis Sci. 2019 Sep 3;60(12):3878-3886. doi: 10.1167/iovs.19-27113.

DOI:10.1167/iovs.19-27113
PMID:31529082
Abstract

PURPOSE

To test the hypothesis that the capacity for retinal ganglion cells to functionally recover from chronic IOP elevation is dependent on the duration of IOP elevation.

METHODS

IOP elevation was induced in one eye in anesthetized (isoflurane) adult C57BL6/J mice using a circumlimbal suture. Sutures were left in place for 8 and 16 weeks (n = 30 and 28). In two other groups the suture was cut after 8 and 12 weeks (n = 30 and 28), and ganglion cell function (electroretinography) and retinal structure (optical coherence tomography) were assessed 4 weeks later. Ganglion cell density was quantified by counting RBPMS (RNA-binding protein with multiple splicing)-stained cells.

RESULTS

With IOP elevation (∼10 mm Hg above baseline), ganglion cell function declined to 75% ± 8% at 8 weeks and 59% ± 4% at 16 weeks relative to contralateral control eyes. The retinal nerve fiber layer was thinner at 8 (84% ± 4%) and 16 weeks (83% ± 3%), without a significant difference in total retinal thickness. Ganglion cell function recovered with IOP normalization (suture removal) at week 8 (97% ± 7%), but not at week 12 (73% ± 6%). Ganglion cell loss was found in all groups (-8% to -13%).

CONCLUSIONS

In the mouse circumlimbal suture model, 12 weeks of IOP elevation resulted in irreversible ganglion cell dysfunction, whereas retinal dysfunction was fully reversible after 8 weeks of IOP elevation.

摘要

目的

验证视网膜神经节细胞(RGC)从慢性眼压升高中恢复功能的能力取决于眼压升高持续时间的假说。

方法

在麻醉(异氟烷)的成年 C57BL6/J 小鼠中,通过环扎缝线在一只眼上引起眼压升高。缝线放置 8 周和 16 周(n = 30 和 28)。在另外两组中,缝线在 8 周和 12 周后被剪断(n = 30 和 28),并且在 4 周后评估了 RGC 功能(视网膜电图)和视网膜结构(光学相干断层扫描)。通过计数 RBPMS(多剪接 RNA 结合蛋白)染色细胞来量化 RGC 密度。

结果

随着眼压升高(比基线高约 10mmHg),RGC 功能在 8 周时下降至对照眼的 75%±8%,在 16 周时下降至 59%±4%。在 8 周(84%±4%)和 16 周(83%±3%)时,神经纤维层变薄,而总视网膜厚度无显著差异。在 8 周时(97%±7%),通过眼压正常化(缝线去除)恢复了 RGC 功能,但在 12 周时(73%±6%)没有恢复。在所有组中都发现了 RGC 丢失(-8%至-13%)。

结论

在小鼠环扎缝线模型中,12 周的眼压升高导致 RGC 功能不可逆转的丧失,而在眼压升高 8 周后,视网膜功能完全可逆。

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