Marangoz Deniz, Guzel Elif, Eyuboglu Signem, Gumusel Asli, Seckin Ismail, Ciftci Ferda, Yilmaz Bayram, Yalvac Ilgaz
Department of Ophthalmology, Faculty of Medicine, Yeditepe University, Sakir Kesebir cad. Gazi Umur Pasa sok. No: 28, 34349, Beşiktaş-Istanbul, Turkey.
Department of Histology and Embryology, Cerrahpasa Faculty of Medicine, Istanbul University, Kocamustafapasa cad., 34098, Fatih-Istanbul, Turkey.
Int Ophthalmol. 2018 Dec;38(6):2553-2562. doi: 10.1007/s10792-017-0768-z. Epub 2017 Nov 20.
We aimed to compare the neuroprotective effects of brimonidine tartrate (BRT) and melatonin (MEL) on retinal ganglion cells (RGCs) in a rat glaucoma model.
Thirty-six adult Wistar albino rats were allocated into six groups: control (C), glaucoma (G), BRT, MEL, G + BRT and G + MEL. After establishing the glaucoma model, intraocular pressure (IOP) of all animals measured at day 4 and day 30 was compared statistically with day 0 and day 4, respectively. Prior to sacrification at day 30 for histological evaluation and TUNEL analysis, retrograde labeling of non-apoptotic RGCs with 3% Fluorogold was performed and RGCs were evaluated under fluorescein microscope.
IOP measurements at day 4 were significantly higher than basal measurements in all glaucoma groups. BRT alone induced a time-dependent decrease in IOP (p < 0.05), while MEL alone failed to reduce IOP. However, both BRT and MEL reduced IOP in the presence of glaucoma at day 30 (p < 0.05). BRT treatment significantly reversed the reduced non-apoptotic RGC counts (p < 0.01) and increased TUNEL-positive RGCs (p < 0.001) to control group levels in the presence of glaucoma. However, no statistical significance was found between groups G and G + MEL considering 3% Fluorogold-labeled cell counts and apoptotic index values.
Our study revealed that systemic administration of BRT also has an IOP reducing effect. MEL has no neuroprotective effect on RGCs; on the other hand, BRT acts as a neuroprotective agent against glaucomatous injury, when applied systemically.
我们旨在比较酒石酸溴莫尼定(BRT)和褪黑素(MEL)对大鼠青光眼模型视网膜神经节细胞(RGCs)的神经保护作用。
将36只成年Wistar白化大鼠分为六组:对照组(C)、青光眼组(G)、BRT组、MEL组、G + BRT组和G + MEL组。建立青光眼模型后,分别将所有动物在第4天和第30天测得的眼压与第0天和第4天进行统计学比较。在第30天处死动物进行组织学评估和TUNEL分析之前,用3%荧光金对未凋亡的RGCs进行逆行标记,并在荧光显微镜下评估RGCs。
所有青光眼组在第4天测得的眼压均显著高于基础眼压测量值。单独使用BRT可使眼压随时间下降(p < 0.05),而单独使用MEL未能降低眼压。然而,在第30天青光眼存在的情况下,BRT和MEL均降低了眼压(p < 0.05)。在青光眼存在的情况下,BRT治疗显著逆转了未凋亡RGC计数的减少(p < 0.01),并使TUNEL阳性RGCs增加(p < 0.001)至对照组水平。然而,考虑到3%荧光金标记的细胞计数和凋亡指数值,G组和G + MEL组之间未发现统计学差异。
我们的研究表明,全身应用BRT也有降低眼压的作用。MEL对RGCs没有神经保护作用;另一方面,全身应用时,BRT可作为一种抗青光眼损伤的神经保护剂。