Ponjavic Vesna, Gränse Lotta, Kjellström Sten, Andréasson Sten, Bruun Anitha
Department of Ophthalmology, Wallenberg Retina Center, University of Lund, Lund, Sweden.
Doc Ophthalmol. 2004 Mar;108(2):125-33. doi: 10.1023/b:doop.0000036780.96560.74.
To determine whether long-term treatment with the anti-epileptic drug vigabatrin causes damage to rabbit retina.
Five rabbits were treated continuously with a daily dose of vigabatrin solution per orally during a period of 1-8 months. Two rabbits receiving water were used as controls. Repeated full-field electroretinograms (every two weeks) were assessed during this period. Vigabatrin serum concentration was repeatedly measured for securing successful drug administration. After termination of treatment the rabbits were sacrificed and the morphology of the sectioned retina was studied.
In all rabbits treated with vigabatrin the serum analyses repeatedly demonstrated elevated drug concentration. Full-field electroretinograms demonstrated normal rod function in all treated rabbits, but reduced cone function in two of the five treated rabbits verified by 30Hz flicker stimulation. Morphologic studies of the sectioned retina demonstrated GFAP immunoactivity of the glial cells localized in the retinal periphery in all five treated rabbits, one of which had staining also in the centrally localized glial cells. The treated rabbits also demonstrated a weaker GAD staining in the IPL and less positive amacrine cells, compared to the controls. Only two treated rabbits had normal GABA staining while three had an enhanced GABA immunoreactivity and undistinguishable fibers in the IPL. In three out of five treated rabbits the Müller cells were short, stubby and fragmented, with swollen endfeet.
This study demonstrates changes in histopathology caused by vigabatrin in an animal model, which has not been reported previously. We have found that vigabatrin orally administrated to rabbits does not affect rod function but may reduce cone function in the full-field electroretinogram, which is similar to the previously reported vigabatrin effect on the human ERG. The results indicate that vigabatrin may damage or influence, at least one cell type in the rabbit retina.
确定抗癫痫药物氨己烯酸的长期治疗是否会对兔视网膜造成损害。
5只兔子连续1 - 8个月每日口服氨己烯酸溶液。2只接受水的兔子作为对照。在此期间重复进行全视野视网膜电图检查(每两周一次)。反复测量氨己烯酸血清浓度以确保药物给药成功。治疗结束后处死兔子,研究视网膜切片的形态。
在所有接受氨己烯酸治疗的兔子中,血清分析反复显示药物浓度升高。全视野视网膜电图显示所有接受治疗的兔子杆细胞功能正常,但通过30Hz闪烁刺激证实,5只接受治疗的兔子中有2只锥细胞功能降低。视网膜切片的形态学研究显示,所有5只接受治疗的兔子视网膜周边的神经胶质细胞均有胶质纤维酸性蛋白(GFAP)免疫活性,其中1只兔子中央定位的神经胶质细胞也有染色。与对照组相比,接受治疗的兔子在视网膜内网层(IPL)的谷氨酸脱羧酶(GAD)染色也较弱,无长突细胞阳性较少。只有2只接受治疗的兔子GABA染色正常,而3只兔子的GABA免疫反应性增强,IPL中的纤维难以区分。5只接受治疗的兔子中有3只的米勒细胞短而粗且破碎,终足肿胀。
本研究证明了氨己烯酸在动物模型中引起的组织病理学变化,这在以前尚未见报道。我们发现,给兔子口服氨己烯酸不影响杆细胞功能,但可能会降低全视野视网膜电图中的锥细胞功能,这与先前报道的氨己烯酸对人视网膜电图的影响相似。结果表明,氨己烯酸可能会损害或影响兔视网膜中的至少一种细胞类型。