Rangaswamy Nalini V, Frishman Laura J, Dorotheo E Ulysses, Schiffman Jade S, Bahrani Hasan M, Tang Rosa A
College of Optometry, University of Houston, Houston, Texas 77204-2020, USA.
Invest Ophthalmol Vis Sci. 2004 Oct;45(10):3827-37. doi: 10.1167/iovs.04-0458.
To determine whether anterior ischemic optic neuropathy and compressive optic neuropathy in humans alter the photopic flash ERG and to investigate the cellular origins of the waves that are affected by pharmacologic agents in primates.
Photopic flash ERGs were recorded differentially, with DTL electrodes, between the two eyes of 22 patients with diagnosed optic neuropathy (n = 17, anterior ischemic optic neuropathy [AION]; n = 5, compressive optic neuropathy) and 25 age-matched control subjects and in 17 eyes of 13 monkeys (Macaca mulatta). The stimulus consisted of brief (<5 ms) red (lambda(max) = 660 nm) Ganzfeld flashes (energy range, 0.5-2.0 log td-s) delivered on a rod-saturating blue background of 3.7 log sc td (lambda(max) = 460 nm). An eye of the patient with ischemic changes at the disc was classified as symptomatic if it showed visual field defects with a mean deviation (MD) of P < 2%. Recordings in macaque monkeys were made before and after inner retinal blockade with tetrodotoxin (TTX) (1.2-2.1 microM; n = 7), TTX+N-methyl-d-aspartate (NMDA; 1.4-6.4 mM; n = 7), and cis-2, 3 piperidine dicarboxylic acid (PDA; 3.3-3.8 mM; n = 3).
The PhNR amplitude was significantly reduced in both symptomatic (P = 3.4 x 10(-8)) and asymptomatic (P = 0.036) eyes of patients with AION or compressive optic neuropathy (P = 0.0054) compared with control subjects. The PhNR amplitude in the symptomatic eye showed a moderate correlation with field defects (P < 0.05) similar to previous findings in open-angle glaucoma. The a-wave also was reduced significantly in the symptomatic eye (P = 0.0002) of patients with AION. The i-wave, a positive wave on the trailing edge of the b-wave peaking around 50 ms, became more prominent in eyes in which the PhNR was significantly reduced. In monkeys, the PhNR was eliminated by TTX. The a-wave at the peak and later times was reduced by TTX, further reduced by NMDA, and eliminated after PDA in response to the red stimuli. PDA also eliminated the i-wave.
PhNR amplitude is significantly reduced in eyes with open-angle glaucoma, AION, and compressive optic neuropathy. Experiments in primates indicate that this reduction reflects loss of a spike-driven contribution to the photopic ERG. There also are small spike-driven contributions to the a-wave elicited by full-field red stimuli. The i-wave, which becomes more prominent when the PhNR is reduced, has origins in the off-pathway distal to the ganglion cells.
确定人类前部缺血性视神经病变和压迫性视神经病变是否会改变明视闪光视网膜电图,并研究在灵长类动物中受药物影响的波形的细胞起源。
使用DTL电极,对22例诊断为视神经病变的患者(n = 17,前部缺血性视神经病变[AION];n = 5,压迫性视神经病变)和25名年龄匹配的对照受试者的双眼进行差异明视闪光视网膜电图记录,并对13只猕猴(恒河猴)的17只眼睛进行记录。刺激由短暂(<5毫秒)的红色(λmax = 660纳米)全视野闪光(能量范围,0.5 - 2.0对数td - s)组成,在3.7对数sc td(λmax = 460纳米)的杆饱和蓝色背景上呈现。如果视盘有缺血改变的患者的眼睛出现平均偏差(MD)P < 2%的视野缺损,则将其分类为有症状。在用河豚毒素(TTX)(1.2 - 2.1微摩尔;n = 7)、TTX + N - 甲基 - d - 天冬氨酸(NMDA;1.4 - 6.4毫摩尔;n = 7)和顺式 - 2,3 - 哌啶二羧酸(PDA;3.3 - 3.8毫摩尔;n = 3)对内视网膜进行阻断前后,对猕猴进行记录。
与对照受试者相比,AION或压迫性视神经病变患者的有症状(P = 3.4×10−8)和无症状(P = 0.036)眼睛的PhNR振幅均显著降低(P = 0.0054)。有症状眼睛的PhNR振幅与视野缺损呈中度相关性(P < 0.05),类似于先前在开角型青光眼中的发现。AION患者有症状眼睛的a波也显著降低(P = 0.0002)。i波是b波后沿约50毫秒处达到峰值的正向波,在PhNR显著降低的眼睛中变得更加突出。在猕猴中,TTX消除了PhNR。红色刺激下,TTX使a波在峰值及之后的时间降低,NMDA使其进一步降低,PDA后消除。PDA也消除了i波。
开角型青光眼、AION和压迫性视神经病变患者的眼睛中PhNR振幅显著降低。灵长类动物实验表明,这种降低反映了对明视视网膜电图的尖峰驱动贡献的丧失。全视野红色刺激引起的a波也有小的尖峰驱动贡献。当PhNR降低时变得更加突出的i波起源于神经节细胞远端的离通路。