Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Glostrup, Denmark.
Invest Ophthalmol Vis Sci. 2012 Sep 14;53(10):6207-13. doi: 10.1167/iovs.12-10110.
The objective of the study was to investigate the effect of glial cell line-derived neurotrophic factor (GDNF) on the multifocal electroretinogram (mfERG) following an induced branch retinal vein occlusion (BRVO) in pigs.
Electrophysiological examination of the retina was performed in 20 pigs with standard and four-frame mfERG 4 weeks after induced BRVO and intravitreal injection of GDNF or vehicle. BRVO was induced by intraocular diathermia of the superior retinal vein. Inner retinal function was measured by analysis of the four-frame mfERG (iN1) and outer retinal function with standard mfERG (P1).
In GDNF-treated BRVO eyes, P1 and iN1 amplitudes (P = 0.51 and 0.78) or implicit times (P = 0.08 and 0.99) did not differ from those in healthy fellow eyes. After vehicle injection, P1 and iN1 amplitudes of BRVO eyes were significantly lower than in the healthy fellow eye (P = 0.022 and 0.013). The log ratios of mfERG amplitudes between experimental and healthy fellow eyes were calculated (BRVO/healthy). GDNF improved the ratios of the four-frame mfERG (1.29 [0.88-1.88]) compared with vehicle (0.32 [0.21-0.50], P < 0.001). Equally, GDNF improved the ratios of the standard mfERG; GDNF (0.75 [0.51-1.10]) and vehicle (0.42 [0.27-0.63], P = 0.048).
GDNF appears neuroprotective on retinal electrophysiological function after BRVO. The efficacy and safety of GDNF remain to be investigated in primate eyes.
本研究旨在探讨胶质细胞源性神经营养因子(GDNF)对猪诱导性分支视网膜静脉阻塞(BRVO)后多焦视网膜电图(mfERG)的影响。
在诱导性 BRVO 及玻璃体内注射 GDNF 或载体 4 周后,对 20 只猪进行视网膜标准和 4 帧 mfERG 电生理检查。通过眼内加热上视网膜静脉诱导 BRVO。通过分析 4 帧 mfERG(iN1)测量内视网膜功能,通过标准 mfERG(P1)测量外视网膜功能。
在 GDNF 治疗的 BRVO 眼中,P1 和 iN1 振幅(P = 0.51 和 0.78)或潜伏期(P = 0.08 和 0.99)与健康对侧眼无差异。在载体注射后,BRVO 眼的 P1 和 iN1 振幅明显低于健康对侧眼(P = 0.022 和 0.013)。计算 mfERG 振幅实验眼与健康对侧眼的对数比值(BRVO/健康对侧眼)。与载体相比,GDNF 提高了 4 帧 mfERG 的比值(1.29 [0.88-1.88])(P < 0.001)。同样,GDNF 提高了标准 mfERG 的比值;GDNF(0.75 [0.51-1.10])和载体(0.42 [0.27-0.63],P = 0.048)。
GDNF 似乎对 BRVO 后视网膜电生理功能具有神经保护作用。GDNF 在灵长类动物眼中的疗效和安全性仍需进一步研究。