April 2012
Volume 53, Issue 4
Free
Glaucoma  |   April 2012
Structure/Function Studies and the Effects of Memantine in Monkeys with Experimental Glaucoma
Author Affiliations & Notes
  • B'Ann T. Gabelt
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • Carol A. Rasmussen
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • Ozan Y. Tektas
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • Charlene B. Y. Kim
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • John C. Peterson
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • T. Michael Nork
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • James N. Ver Hoeve
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • Elke Lütjen-Drecoll
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • Paul L. Kaufman
    From the Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and the Anatomy Institute LS II, University of Erlangen-Nürnberg, Erlangen, Germany.
  • Corresponding author: Paul L. Kaufman, University of Wisconsin-Madison, Ophthalmology and Visual Sciences, 2828 Marshall Court, Suite 200, Madison, WI 53705; plkaufma@mhub.ophth.wisc.edu
Investigative Ophthalmology & Visual Science April 2012, Vol.53, 2368-2376. doi:10.1167/iovs.11-8475
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      B'Ann T. Gabelt, Carol A. Rasmussen, Ozan Y. Tektas, Charlene B. Y. Kim, John C. Peterson, T. Michael Nork, James N. Ver Hoeve, Elke Lütjen-Drecoll, Paul L. Kaufman; Structure/Function Studies and the Effects of Memantine in Monkeys with Experimental Glaucoma. Invest. Ophthalmol. Vis. Sci. 2012;53(4):2368-2376. doi: 10.1167/iovs.11-8475.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose.: The scanning laser polarimetry with variable corneal compensation (GDx VCC) methodology was established and verified in monkeys with experimental glaucoma (ExpG). Terminal GDx parameters were correlated with axon counts and electrophysiologic measures. The effects of memantine on these parameters were investigated.

Methods.: ExpG was induced in monkeys and intraocular pressure monitored weekly. Some monkeys received memantine in their diet before and after ExpG induction (1–10 months). GDx VCC scans, stereophotographs, and multifocal visual evoked potential (mfVEP) data were collected at baseline and every 6 to 8 weeks until euthanasia. Optic nerves were prepared for axon counting and other morphologic analysis.

Results.: There was no difference in IOP elevation exposure between memantine-treated and no-memantine–treated monkeys. The percentage of the optic nerve area composed of connective tissue septa was significantly greater in ExpG eyes than in Fellow eyes. There was a strong positive correlation between axon counts and terminal GDx parameter measures. Animals not receiving memantine exhibited significantly lower mfVEP amplitudes in ExpG eyes compared with the ipsilateral baseline or the final value in the Fellow eye. ExpG eyes from memantine-treated animals had higher overall mean amplitudes that were not significantly different relative to the ipsilateral baseline and final amplitudes in the Fellow eye.

Conclusions.: The authors' studies confirm that GDx VCC can be utilized in monkey ExpG studies to detect early retinal structural changes and that these changes are highly correlated with optic nerve axon counts. These structural changes may or may not lead to central functional changes as shown by the mfVEP in response to investigational therapies.

Introduction
Glaucoma is an optic neuropathy characterized by the pathological loss of retinal ganglion cells (RGCs) and their axons. 1 The experimental glaucoma (ExpG) model in nonhuman primates 2 is useful for evaluating potential therapies for human glaucomatous optic neuropathy. 3 It is the most objective model for evaluating the correlation of various diagnostic measures for glaucoma since the glaucoma eye can be compared with the control eye of a single subject. Ocular tissue can be collected immediately after death at various stages of damage. 4  
In glaucoma, the loss of RGCs can be detected structurally as a thinning of the retinal nerve fiber layer (RNFL) and neuroretinal rim. 5 Several imaging technologies have been developed to evaluate the optic disk and RNFL. 6 Scanning laser polarimetry with variable corneal compensation (GDx VCC) is one technology that has been used successfully in humans to follow progressive RNFL loss in glaucoma patients that show progression in optic disc stereophotographs or mild to moderate visual field defects. 7,8  
Adaptation of imaging technologies for use with nonhuman primates can be challenging because of their inability to fixate on a target if anesthesia is used. Alternatively, monkeys may be trained to fixate on a target after considerable investment in time. However, the numbers of other parameters to be measured and the required experimental manipulations may not be practical with a conscious model. 
We describe here a technique for obtaining reproducible scanning laser polarimetry measurements in the anesthetized nonhuman primate with ExpG. 
In addition, many of the monkeys used in the current study were originally part of a follow-up to the studies of Hare. 9,10 Some of the current monkeys were fed memantine, an NMDA glutamate open-channel blocker that may rescue neurons through its blockade of excessive glutamate receptor activation, 1113 for the duration of their ExpG. Early endpoints in ExpG were used, and correlations between elevated IOP exposure, axon loss, GDx VCC and electrophysiology parameters, and effects of memantine on those measures were also investigated. 
Materials and Methods
All animal studies were performed in accordance with institutional guidelines approved by the University of Wisconsin Research Animal Resources Center and in adherence to the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research. 
Cynomolgus monkeys ( Macaca fascicularis ) of either sex, weighing 2.3 to 6.9 kg were studied. ExpG was induced unilaterally in 25 monkeys by laser scarification of the trabecular meshwork, 2,14 with a target IOP of 30 to 40 mmHg. IOP was monitored weekly under ketamine anesthesia by Goldmann applanation tonometry 15,16 and occasionally with a Tonopen. 17 GDx VCC scans, stereophotographs, and multifocal visual evoked potential (mfVEP) data were collected at baseline and every 6 to 8 weeks until euthanasia. Not all monkeys received all tests. 
Prior to lasering and after ExpG induction (1–11 months), 11 monkeys were started on a diet containing memantine (1-amino-3,5-dimethyladamantane; Allergan, Inc., Irvine, CA) in fruit, beginning at 2 mg/kg/day and ramping up over a 4-week period to 8 mg/kg/day). The remaining monkeys (no memantine) were either fed fruit or received no treatment.Plasma samples were collected at baseline and after 1 week at the 8 mg/kg dosage and every 6 to 8 weeks thereafter. These were analyzed at Allergan, Inc., using an internal standard method in combination with HPLC as described previously. 9 A target plasma concentration of 1 μM was desired prior to lasering. 
When there was detectable loss of optic nerve head tissue in ExpG monkeys that did not receive memantine, as assessed by stereo-biomicroscopic examination, monkeys were anesthetized with pentobarbital anesthesia and euthanized by exsanguination with PBS followed by perfusion through the heart with 2% to 4% paraformaldehyde. Optic nerves were prepared for axon counting and morphologic analysis. 
GDx VCC
For establishing the techniques and to evaluate GDx parameters for use in monkeys, 12 monkeys with unilateral ExpG (eight from the group above and four additional female cynomolus [6–7 years old from an unrelated study]) and one rhesus monkey (female, 21 years with elevated IOP resulting from intraocular manipulations as part of another study) were used. Data from these last five monkeys were included only in Table 1. Parameters that were evaluated included the coefficient of variation of common measures, effects of lens opacity on the coefficient of variation, image quality with and without contact lenses measured on the same day, and correlation with cup-to-disc (c/d) ratio. 
Table 1.
 
GDx VCC Parameters Versus c/d Changes in ExpG
Table 1.
 
GDx VCC Parameters Versus c/d Changes in ExpG
Δc/d
Control Eyes 0–0.1 0.15–0.2 ≥ 0.4
N = 9 N = 9 N = 7 N = 4
TSNIT ellipse avg. 52.96 ± 1.99 48.74 ± 1.52 47.55 ± 2.96 37.68 ± 3.80
Avg. thickness 45.00 ± 1.49 42.67 ± 1.11 41.86 ± 2.22 36.75 ± 2.95
Superior avg. 64.56 ± 2.99 61.28 ± 2.57 56.63 ± 4.54 40.37 ± 2.47
Inferior avg. 59.11 ± 2.74 55.48 ± 2.09 51.94 ± 3.82 39.57 ± 5.79
SD 22.80 ± 2.05 21.97 ± 1.31 18.30 ± 1.94 9.43 ± 1.87
Change from baseline
TSNIT ellipse avg. 0.10 ± 0.31 −3.86 ± 0.96* −6.12 ± 2.35* −12.74 ± 4.28
Avg. thickness −0.05 ± 0.28 −2.78 ± 1.04* −3.31 ± 1.83 −6.92 ± 4.12
Superior avg. 0.03 ± 0.46 −5.30 ± 1.89* −9.57 ± 3.02* −18.67 ± 4.61*
Inferior avg. 0.59 ± 0.53 −4.01 ± 1.39* −9.06 ± 3.22* −19.72 ± 5.51*
SD 0.19 ± 0.46 −2.95 ± 0.94* −6.73 ± 1.19* −14.30 ± 2.91*
Table 2.
 
Terminal GDx VCC Values for Axon Comparisons in Figure 2
Table 2.
 
Terminal GDx VCC Values for Axon Comparisons in Figure 2
GDx VCC Parameter (μm)
TSNIT (Ellipse Average) Average Thickness Superior Average Inferior Average
Monkey No. ExpG Cont ExpG Cont ExpG Cont ExpG Cont
K568 56.38 66.46 49.00 57.00 62.34 81.62 70.83 79.18
K639 37.67 55.23 36.00 47.00 44.67 63.73 41.20 61.11
K640 45.84 54.27 41.00 47.00 56.32 72.44 50.55 61.11
K560 31.02 53.38 30.00 46.00 42.10 62.30 25.94 60.89
K564 33.96 50.57 32.00 43.00 38.92 65.54 31.07 52.87
K576 42.48 47.06 40.00 42.00 39.34 39.21 51.31 53.41
K630 46.17 46.32 42.00 42.00 58.28 55.13 49.48 53.97
K645 50.07 52.63 44.00 46.00 68.48* 54.38 51.28 60.24
For GDx measurements, monkeys were anesthetized with a combination of intramuscular ketamine (10–15 mg/kg) and intramuscular medetomidine (30–60 μg/kg), followed by inhalation isoflurane. Monkeys were maintained at, or near, surgical anesthetic depth for the scanning procedure. IOP (Goldmann applanation tonometer), corneal curvature (Reichert keratometer), and refraction (Hartinger-coincidence) were measured at each session. Axial length measurements (Sonomed A5500 A-Scan; Sonomed, Inc., Lake Success, NY) were taken at some time points. Slit-lamp biomicroscopic examinations were performed monthly. A 10-mm plano contact lens was applied to ensure adequate corneal hydration and clarity. Refraction and curvature measurements were repeated after application of the lens, and values were entered into the patient focal correction field. A motorized head-holder with remote control was used to make fine adjustments in position to facilitate matching alignment to the baseline image. A GDx1 VCC prototype system (Laser Diagnostic Technology, San Diego, CA) was used to acquire nerve fiber layer (NFL) thickness measurements. 18 Corneal compensation was calculated at baseline and verified by three or more compensated macular scans at each time point. A new compensation was calculated if retardance or corneal axis values were variable. During each session, three to five separate peripapillary scans were taken and a mean was created. The scan head was realigned between scans to generate discrete images. Variability (coefficient of variation) for the parameters was determined for Fellow normal eyes during intervals of 22 to 36 days, during which eyes were scanned three or four times. The GDx VCC system and parameters are described in greater detail elsewhere. 1921  
Stereoscopic color fundus photographs were taken on each scan day and used to evaluate the c/d ratio for each eye. If animals had both horizontal and vertical c/d ratio readings, the latter was used. In some eyes, an average of horizontal and vertical was used, for example, if one eye had horizontal and vertical evaluations and the other did not. IOP was lowered pharmacologically, starting the day before imaging, with Timoptic-XE (0.5% timolol maleate in gel-forming vehicle; Merck & Co., West Point, PA), and if necessary PGF2α-isopropylester (2 μg in 5 μL saline; Cayman Chemical, Ann Arbor, MI), to reverse possible disc cupping because of compliance rather than tissue loss in ExpG eyes. 
Electrophysiology
The mfVEPs were recorded with the methods presented in a recent publication. 22 Root mean square (RMS) signal-to-noise ratio (SNR) determinations of the second-order (first slice) kernel (K2.1) mfVEP response (central 21° of the visual field) were compared in all statistical analyses. Linear regression analysis was applied to the scatter plots, and P values ≤ 0.05 were adopted as the level of significance. t-tests (two sample assuming unequal variances) were carried out on no-memantine and memantine comparisons both at baseline and at study termination. 
Axon Counts and Morphology
Optic nerves of 14 pairs of eyes with unilateral laser-induced ExpG were evaluated morphologically for optic nerve damage. Seven of the animals had been treated with memantine, four were treated with vehicle, and three received no treatment. Because monkeys were in two different groups (each group containing memantine and no-memantine animals) as part of another study and were euthanized at different times, the optic nerve processing varied as conditions were optimized for tissue collection for the parent study. For six monkeys (two memantine, four no-memantine), following exsanguination with PBS and perfusion through the heart with 2% paraformaldehye/0.1M phosphate buffer (PB), pH 7.4, the eyes with optic nerves attached were enucleated and placed in 2% paraformaldehyde/0.1M PB for 3 hours then transferred to 30% sucrose and stored for the parent study. Subsequently, after several months, the optic nerves were transferred to Ito's fixative. 23 For the other eight monkeys (five memantine, three no-memantine), following exsanguination with PBS, the eyes were enucleated, and the optic nerves were dissected 1 to 2 mm behind the globe and placed in Ito's fixative. All of the optic nerves were embedded in Epon and then semithin cross-sectioned with an Ultracut E (Reichert Jung, Vienna, Austria) and subsequently stained with toluidine blue. Sections were viewed with an Aristoplan microscope (Ernst Leitz, Wetzlar, Germany) and photographed with a Leica DC 500 camera (Leica Camera AG, Solms, Germany). Despite the differences in fixation types, the axon quantification was possible except in three Fellow eyes in which the center of the nerve was not preserved well enough for quantification. 
Determination of Optic Nerve Changes
Axon counts were determined in accordance to our previous reports 2427 based on the method of Quigley. 1 Briefly, the area of the entire nerve, excluding the meninges, was measured. The area containing the nerve fiber bundles and the area of connective tissue between the nerve fiber bundles and surrounding the central retinal vessels were measured separately. For determination of the axon number, the cross-section of the optic nerve was divided into eight sectors. In each sector, axons in five sample areas of 1000 μm2 were counted. These sample areas extended from the central to the peripheral nerve at equal distances from each other. The mean of all measurements was multiplied by the nerve fiber area to yield the total axon counts (see Table 4). 
Data Analysis
Linear regression analysis was used to compare correlations between two parameters. 
Area under the Curve
Once IOP in the ExpG eyes was ≥25 mmHg and the difference ExpG-Fellow IOP was ≥5 mmHg initially, then the difference at each time point was plotted versus time. The area under this difference curve was integrated using Sigma Plot v8.0 (Systat Software, Inc., San Jose, CA). 
Paired and Unpaired t-tests
Two-tailed paired and unpaired t-tests compare differences to 0.0 or ratios to 1.0. Significance was designated at P < 0.05. 
Results
IOP and Cumulative IOP Insult
IOP (mean ± SEM) in ExpG eyes from the time of initial elevation of ≥25 mmHg until euthanasia averaged 30.45 ± 1.74 mmHg while Fellow control eyes averaged 16.52 ± 0.36 mmHg (n = 27). In no-memantine ExpG eyes, IOP during the same interval was 32.29 ± 2.54mmHg. In memantine ExpG eyes, the corresponding IOP was 28.11 ± 2.23 mmHg. Cumulative IOP Insult (CII, mmHg × days) analysis for ExpG and Fellow control eyes showed that for all monkeys in the study, there was a tendency toward but no significant difference in IOP elevation exposure comparing memantine-treated and no-memantine–treated monkeys (CII memantine = 1276 ± 240; CII no-memantine = 1804 ± 283, P = 0.183, unpaired t-test). Also, the average IOP difference between ExpG and Fellow eyes calculated by CII/days was no different comparing memantine-treated and no-memantine–treated monkeys (mean mmHg difference, memantine = 12.6 ± 2.1; no-memantine = 15.5 ± 2.3, P = 0.36, unpaired t-test). 
Serum memantine ranged from 0.4 to 3.9 μM over the duration of the study. 
GDx VCC
Figure 1 is an example of a GDx VCC scan in monkey K560 with ExpG in the right eye demonstrating severe nerve fiber layer thinning. Table 1 shows a progressive decrease in commonly examined GDx VCC parameter values relative to baseline as the c/d ratio increased in ExpG eyes. Mean intersession coefficients of variation for these parameters measured three to four times in four Fellow eyes without lens opacities during a 22- to 36-day interval ranged from 3.5% to 5.5%. Lens opacities slightly increased the coefficient of variation (clear lens vs. opacity: average thickness, 3.5% vs. 4.2%; TSNIT SD, 5.0% vs. 11.8%; inferior average, 5.5% vs. 7.3%). Image-quality scores, which reflect overall image quality, image intensity, image vignetting, illumination, and contrast, were greatly improved when a contact lens was used (e.g., 4/35 failures [scores less than 70 out of 100] with a contact lens vs. 16/35 failures in the same seven eyes without a contact lens). Significant changes were detected comparing baseline and terminal refractions (diopters ± SEM) in ExpG eyes (baseline, −1.11 ± 0.26; terminal −2.67 ± 0.47, P = 0.002, n = 9). 
Figure 1.
 
Example of a GDx VCC scan from a monkey with ExpG. The GDx scan for monkey K560 shows severe thinning of the nerve fiber layers in the superior and inferior quadrants of the glaucomatous right eye (see also Table 2 for terminal GDx VCC values).
Figure 1.
 
Example of a GDx VCC scan from a monkey with ExpG. The GDx scan for monkey K560 shows severe thinning of the nerve fiber layers in the superior and inferior quadrants of the glaucomatous right eye (see also Table 2 for terminal GDx VCC values).
Figure 2.
 
TSNIT or average thickness changes in ExpG compared with Fellow eyes as a function of axon counts. Common GDx measures were highly correlated with percent change (%Δ) in axon counts in ExpG versus Fellow eyes (A, B) and with actual axon counts in ExpG eyes (C, D). The absolute value of GDx measures considering all eyes was also correlated with axon counts (E, F). Similar correlations were found with other GDx measures (superior average and inferior average). More axon count values were available for ExpG eyes than for Fellow eyes (open symbols indicate ExpG eyes where there were no corresponding Fellow eye axon counts, also see Table 4).
Figure 2.
 
TSNIT or average thickness changes in ExpG compared with Fellow eyes as a function of axon counts. Common GDx measures were highly correlated with percent change (%Δ) in axon counts in ExpG versus Fellow eyes (A, B) and with actual axon counts in ExpG eyes (C, D). The absolute value of GDx measures considering all eyes was also correlated with axon counts (E, F). Similar correlations were found with other GDx measures (superior average and inferior average). More axon count values were available for ExpG eyes than for Fellow eyes (open symbols indicate ExpG eyes where there were no corresponding Fellow eye axon counts, also see Table 4).
Figure 3.
 
Morphology of optic nerve damage as a result of ExpG. (AC) Schematic drawings showing typical distributions of severely damaged (red), slightly damaged (blue), and histologically unchanged (white) areas in eyes with axon counts of (A) approximately 800,000; (B) approximately 500,000 to 600,000; and (C) approximately 400,000–500,000. (DF) Semithin cross-sections of optic nerves (Richardson's stain). (D) Micrograph of a less damaged area (blue areas in the schematic drawings AC). The nerve fiber bundles are still separated from each other by connective tissue septae (arrows), which, at places, are thickened and show a thickened sheath of glial cells (asterisks). Singular axons are destroyed and appear as spherical inclusions of myelin figures (arrowheads). (E) Micrograph of a severely damaged area (red areas in the schematic drawings AC). Parts of the connective tissue septae appear destroyed (arrows) and displaced by numerous cells with large nuclei (asterisk). In the region of the previous bundles, remnants of myelin (arrowheads) are present. (F) Normal unaffected region of a nerve with the nerve fiber bundles separated from each other by connective tissue septae (arrows).
Figure 3.
 
Morphology of optic nerve damage as a result of ExpG. (AC) Schematic drawings showing typical distributions of severely damaged (red), slightly damaged (blue), and histologically unchanged (white) areas in eyes with axon counts of (A) approximately 800,000; (B) approximately 500,000 to 600,000; and (C) approximately 400,000–500,000. (DF) Semithin cross-sections of optic nerves (Richardson's stain). (D) Micrograph of a less damaged area (blue areas in the schematic drawings AC). The nerve fiber bundles are still separated from each other by connective tissue septae (arrows), which, at places, are thickened and show a thickened sheath of glial cells (asterisks). Singular axons are destroyed and appear as spherical inclusions of myelin figures (arrowheads). (E) Micrograph of a severely damaged area (red areas in the schematic drawings AC). Parts of the connective tissue septae appear destroyed (arrows) and displaced by numerous cells with large nuclei (asterisk). In the region of the previous bundles, remnants of myelin (arrowheads) are present. (F) Normal unaffected region of a nerve with the nerve fiber bundles separated from each other by connective tissue septae (arrows).
There was strong positive correlation between the percentage change (100% × [ExpG − Cont]/Cont) in GDx parameters from scans taken just prior to euthanasia compared with the axon loss ratio (Figs. 2A, 2B, Table 2). Strong correlations were also found with the percentage change in GDx parameters in the ExpG eyes and the actual axon counts (Figs. 2C, 2D) as well as with the actual GDx parameter values for all eyes and the actual axon counts (Figs. 2E, 2F). 
Nerve fiber layer thickness was significantly decreased in ExpG compared with Fellow eyes in both memantine and no-memantine groups (Table 3). There were no significant differences in GDx VCC parameters comparing ExpG eyes from memantine-treated and no-memantine–treated monkeys by the unpaired t-test. Data are from terminal scans closest to the date of euthanasia. 
Table 3.
 
Terminal GDx VCC Parameters: No-Memantine Versus Memantine
Table 3.
 
Terminal GDx VCC Parameters: No-Memantine Versus Memantine
ExpG Fellow ExpG BL Fellow BL
No memantine (n = 7)
TSNIT 44.11 ± 3.77†‡ 55.20 ± 2.08* 50.69 ± 1.20 51.74 ± 1.61
Avg. thickness 39.00 ± 2.81†‡ 47.29 ± 1.90* 43.14 ± 1.24 44.14 ± 1.61
Superior avg. 52.62 ± 4.41*†‡ 67.99 ± 2.74* 62.32 ± 1.51 63.65 ± 1.57
Inferior avg. 50.08 ± 5.33 61.38 ± 3.16 57.30 ± 1.74 59.20 ± 2.75
Memantine (n = 8)
TSNIT 41.45 ± 2.58† 50.28 ± 1.47 49.77 ± 1.49 51.03 ± 1.46
Avg. thickness 37.25 ± 1.84† 43.38 ± 1.12 42.25 ± 1.15 44.08 ± 1.43
Superior avg. 50.69 ± 4.28 58.79 ± 3.44 62.77 ± 2.62 62.25 ± 1.87
Inferior avg. 43.74 ± 4.13*† 57.36 ± 2.26 57.10 ± 1.75 56.46 ± 1.64
Table 4.
 
Axon Counts: No-Memantine Versus Memantine
Table 4.
 
Axon Counts: No-Memantine Versus Memantine
Axon Count Total Optic Nerve Area (mm2) Septa Including Glia (% Optic Nerve Area) Connective Tissue Septa (% Optic Nerve Area)
Monkey No. ExpG Fellow ExpG Fellow ExpG Fellow ExpG Fellow
No memantine
K545 622,640 975,188 4.00 5.71 14.0 n.a. 1.64 1.75
K547 614,813 942,941 4.74 4.94 15.5 10.7 5.22 2.34
K640 823,680 n.a. 7.20 n.a. 10.0 n.a. 3.29 1.67
K568 746,941 922,756 4.38 4.27 8.7 9.4 1.96 2.00
K570 401,857 957,187 5.04 5.65 15.2 7.5 2.65 2.75
K581 563,581 1,053,519 3.97 5.43 16.0 n.a. 2.06 2.55
K639 667,722† 925,936 5.74 5.02 11.2 n.a. 2.83 2.50
Mean 634,462* 962,921 5.01 5.17 12.94 9.20 2.81 2.22
SEM 50,994 19,809 0.43 0.22 1.11 0.93 0.46 0.16
Memantine
K544 612,797 964,429 3.93 4.91 11.0 6.7 4.11 1.91
K549 802,935 n.a. 5.23 4.81 11.0 n.a. 3.61 3.26
K560 475,151 999,648 6.30 6.18 9.3 12.0 2.76 2.98
K564 474,918† 961,779 4.07 4.22 10.3 7.3 1.13 1.07
K576 818,209 n.a 6.51 6.09 14.5 n.a. 3.92 n.a.
K645 828,028† 943,033 5.11 5.90 25.6 16.2 5.60 4.33
K630 1,003,953 1,024,456 4.31 4.14 10.0 8.0 2.89 1.62
Mean 716,570* 990,179 5.07 5.18 13.10 10.04 3.43 2.53
SEM 70,022 16,602 0.39 0.33 2.18 1.80 0.52 0.49
Mean all 675,516* 976,550 5.04 5.17 13.02* 9.73 3.12* 2.36
SEM 45,275 12,989 0.28 0.20 1.17 1.13 0.34 0.24
Optic Nerve Changes and Axon Counts
There were marked differences between animals in the amount of optic nerve damage in the ExpG eyes. The percent change in axon counts in ExpG versus Fellow eyes was correlated with the mean change in IOP exposure with two exceptions in the memantine group. The mean change in IOP was calculated from the CII/duration of IOP elevation from the time IOP was 5 mmHg or more different from the Fellow eye until euthanasia. 
The axon counts in ExpG eyes varied from 400,000 to 500,000 (three eyes), 500,000 to 700,000 (five eyes), and 700,000 to 1,000,000 (six eyes). The distribution of axon damage showed regional differences within the nerve fiber cross-sections. In most nerves with axon counts of 700,000 to 1,000,000, there was a nearly polar orientation of the damaged areas, which were only seen in the periphery of opposing parts of the circumference (Fig. 3A). The morphology of the damaged areas was different in the two regions. In the less damaged areas (blue areas in the schematic drawing), the nerve fiber bundles were still clearly separated from each other by connective tissue septae, which were slightly thickened compared with the normal control eye and showed a thickened sheath of astroglial cells (Fig. 3D). Within the bundles, the size of the astroglial cells appeared increased and there were spherical inclusions of myelin figures (Fig. 3D). 
In areas marked as red in the schematic drawing, parts of the connective tissue septae appeared destroyed and displaced by numerous cells, most of them with large nuclei and some with dark inclusions. In between the cells, remnants of myelin and single myelinated axons were present (Fig. 3E). Most parts of the nerve, however, still appeared unchanged (white areas in Fig. 3A, corresponding to 3F). 
With increasing loss of axons, the morphology of areas drawn blue and red in the schematic drawings were larger. In most eyes with axon counts of 500,000 to 700,000, there were still pronounced regional differences. In three of the five eyes, the center of the nerve was still unchanged. However, nearly the entire periphery showed the severe changes (red, Fig. 3B). This was also true for the other two eyes, but in these eyes slight changes were present throughout the entire cross-section of the nerve. In the three eyes with only 400,000 to 500,000 remaining axons, the entire nerve was damaged but more apparent in the periphery than the center of the nerve (Fig. 3C). 
Axon counts in ExpG eyes both from monkeys that did not receive memantine and from those that did receive memantine were significantly decreased relative to Fellow eyes. There was no significant difference in axon loss comparing ExpG with Fellow eyes from no-memantine– and memantine-treated monkeys (unpaired t-test, P = 0.54) (Table 4). Of the seven eyes treated with memantine, two had axon counts of 400,000 to 500,000, one had counts of 600,000, and four had axon counts between 800,000 and 1,000,000. There were no differences in patterns of axon loss, areas with axon damage, and morphology of these areas in ExpG optic nerves from monkeys that did not receive memantine compared with those that did receive memantine. In all ExpG optic nerves (memantine and no-memantine), the center of the nerve remained unchanged in the less affected eyes, and the periphery was more damaged than the central area. 
The percentage of the optic nerve area composed of connective tissue septa was significantly greater in ExpG than in Fellow eyes from all monkeys examined. There was no difference in the percentage of the optic nerve containing connective tissue septa in ExpG as a result of memantine in the diet. Total optic nerve area was no different in ExpG compared with Fellow eyes. 
Electrophysiology
At baseline, there were no significant differences between the eyes (ExpG or Fellow) in RMS amplitude SNR for either the no-memantine or memantine groups (Table 5). Baseline values for the memantine group were lower (but not significantly) than for the no-memantine group. As expected, in animals that did not receive memantine, the ExpG eyes exhibited significantly lower final RMS amplitude SNR compared with baseline determinations (P = 0.004) and compared with Fellow eyes (P = 0.007). Note also that none of the two-sample t-test statistical comparisons for the memantine group were statistically significant (Baseline ExpG vs. Baseline Fellow; Final ExpG vs. Final Fellow; Baseline ExpG vs. Final ExpG; Baseline Fellow vs. Final Fellow). Final mean amplitudes for memantine ExpG eyes were higher (but not significantly) than were those for no-memantine ExpG eyes. Final amplitudes for Fellow eyes remained lower in the memantine group compared with the no-memantine group, as they did at baseline. 
Table 5.
 
Multifocal VEP K2.1 RMS SNR in ExpG and Fellow Eyes: Baseline and Terminal
Table 5.
 
Multifocal VEP K2.1 RMS SNR in ExpG and Fellow Eyes: Baseline and Terminal
Baseline RMS SNR Final RMS SNR
Monkey No. ExpG Fellow ExpG Fellow
No memantine
K543 5.906 4.522 4.350 3.204
K547 10.899 11.819 4.700 10.863
K568 6.355 5.491 4.795 4.039
K570 9.172 10.966 1.614 12.095
K574 5.920 5.333 3.378 9.475
K639 3.885 10.315 1.752‡ 7.638
K640 5.839 3.831 3.599 9.804
K625 8.379 5.081 5.052 6.465
Mean ± SEM 7.04 ± 0.85 7.17 ± 1.23 3.66 ± 0.51*† 7.95 ± 1.21
Memantine
K541 8.564 7.640 3.586 4.936
K544 7.665 5.106 2.685 11.751
K549 7.575 6.692 1.617 2.920
K560 5.009 6.064 8.554 8.105
K564 11.061 6.839 7.618‡ 3.586
K576 5.162 4.172 5.497 11.029
K630 3.802 11.533 4.470 6.237
K645 4.614 4.472 4.575‡ 2.062
K595 1.968 11.245 3.180 5.368
K608 3.944 2.035 1.708 2.613
Mean ± SEM 5.94 ± 0.91 6.58 ± 1.00 4.35 ± 0.78 5.86 ± 1.15
Discussion
In conducting GDx VCC measurements in nonhuman primates, there are several potential sources of variability that should be monitored. Subjects cannot fixate, so the operator has greater responsibility for alignment. Vigilance is required to align images consistently from one session to the next, as with human patients who do not fixate well or vary in the ability to comfortably position their head and neck from visit to visit. Contact lenses, which increase image quality and are useful to maintain corneal hydration, can change refraction, apparent corneal curvature, and axial length values. There was a tendency in the current study for monkeys to become myopic over time in the ExpG eye. Refraction values cannot be assumed to be constant. This change might impact the computation of some values made by the software. Collecting session-specific information will help assess the impact of this potential source of variability. Collecting multiple discrete scans at each time point, especially at baseline, to get a measure of individual eye variability, can reduce confidence intervals, increasing the likelihood of identifying meaningful change. Inter- and intrasession variability reported in the current study were similar to those obtained in an unrelated study of eyes of 10 normal cynomolgus monkeys (unreported data). 
Terminal GDx parameters, especially TSNIT, were highly correlated with axon counts and c/d ratio changes. The correlation of individual eye GDx parameter values with the corresponding axon counts, although significant, was not as strong as when the GDx results were first expressed as a percentage change in ExpG compared with Fellow eyes (Fig. 2). This suggests that there are individual animal traits that can cause variation in the GDx measures or in the axon counts. Unlike the Hare study, 10 the current study did not detect any memantine-related effects on structural parameters during ExpG. However, only monkeys with the highest mean IOPs were studied by Hare, and the structural measures were done with the Heidelberg Retina Tomograph. The current study also did not detect any significant decrease in optic nerve area, presumably because of the relatively mild loss of axons (<35% loss comparing ExpG to Fellow axon counts) and shorter duration of IOP elevation as compared with other studies. 1,28  
Evidence for a neuroprotective effect of memantine on ganglion cell function in this study could manifest as either enhanced or stabilized mfVEP from ExpG eyes. The authors found that mfVEP from the central stimulus element was sensitive to ExpG: Animals receiving no memantine exhibited significantly lower mfVEP amplitudes in ExpG eyes compared with baseline in the same eye or the final value in the Fellow eye. In contrast, ExpG eyes from memantine-treated animals had higher overall mean amplitudes that were not significantly different relative to baseline in the same eye and final test in the Fellow eye (Table 5). Note that at baseline the mfVEP RMS SNR determinations of the ExpG and Fellow eyes (5.94 ± 0.91 and 6.58 ± 1.00) of the group of animals that were administered memantine tended to be lower (but not significantly) than for the ExpG and Fellow eyes (7.04 ± 0.85 and 7.17 ± 1.23) of the group of animals that did not receive memantine. In addition to inherent variability in mfVEP recordings, memantine plasma levels at the time of sacrifice also were quite variable. Serum levels of memantine were not maintained at the 1 μM level achieved in the Hare studies although early on in their study, levels fluctuated as well. 9  
Given baseline differences, serum memantine levels, and the variability between animals and test sessions in this study, intra-ocular comparisons rather than between-group comparisons are best suited for evaluating the effects of memantine. As noted, there was a significant interocular difference between the mfVEP of ExpG and Fellow eyes of the no-memantine group; however, there was no statistical difference between ExpG and Fellow eyes in memantine-treated animals. The absence of a difference in mfVEP between ExpG and Fellow eyes in the memantine group is therefore consistent with a stabilization of mfVEP of the ExpG eyes, and thus also consistent with, but not probative of, a possible neuroprotective role of memantine on retinal ganglion cells. 
There are several possible reasons why the functional (mfVEP) and structural measures (GDx and axon counts) were not always correlated. Animals with electrophysiologic testing were a smaller subset of the animals with both GDx and axon counts. There are also differences in the variance of the functional and structural measures. The coefficient of variation (SD/mean) for mfVEP RMS SNR is approximately double that of GDx and axon counts. In addition, the relationship between functional and structural measures is not likely to be linear across cell layers or uniform within all animals. Most importantly, the mfVEP measure is derived from the macular stimulus whereas the most severe axonal damage was located in the peripheral optic nerve (Fig. 3). 
Despite these limitations, the authors' mfVEP results are similar to the VEP findings of Hare 9 in that they suggest that memantine may be providing some neuroprotection of the retinal ganglion cells or other cellular structures subserving the central cortical response. In the Hare studies, 9 functional measures demonstrated that memantine treatment delayed but did not prevent the amplitude reduction in the multifocal electroretinogram and visually evoked cortical potential. Amplitude differences were most noticeable at 3 to 5 months after IOP elevation. For monkeys with moderate IOP elevation, memantine treatment was associated with enhanced survival of retinal ganglion cells, especially in the inferior retina. However, they were uncertain if memantine was enhancing the electrophysiology response versus protecting retinal ganglion cells and their axons. It is possible that memantine treatment enhances the ability of surviving retinal ganglion cells to drive activity in the visual cortex, that is, memantine treatment may be associated with plastic changes occurring at more central levels of the visual pathway. Indeed, there was significantly less neuron shrinkage in the lateral geniculate nucleus (LGN) of the memantine-treated than in the vehicle-treated control group even though there was no difference in optic nerve fiber loss. 29 LGN neurons showed reduced dendrite complexity and length that were modified by NMDA receptor blockade with memantine. 30  
As shown by Harwerth, 4 electrophysiologic methods can be as sensitive as standard automated perimetry (SAP) in assessing neural loss from ExpG in nonhuman primates. Visual sensitivity losses were not correlated with retinal ganglion cell losses until a substantial number of neurons were lost. There is a period of progressive neural loss that cannot be detected by SAP as is the case with human glaucoma. 31 However, objective measures such as the photopic negative response, which represents the linear sum of signals from all of the retinal ganglion cells, might detect a proportional decrease in neuronal loss. 4  
At any given point of glaucoma progression, it is speculated that the total retinal ganglion cell population includes a mixed population of normal, dysfunctional, nonviable, and atrophic retinal ganglion cells in various stages of degeneration. Current clinical imaging technologies are capable only of quantifying structural changes in retinal ganglion cell axons but do not specify the level of retinal ganglion cell dysfunction. 32  
Several imaging technologies are now available that are useful for detecting progression during early stages of the glaucoma before functional changes can be detected. 7,3335 Our studies confirm that GDx VCC can be used in monkey ExpG studies to detect early retinal structural changes that may or may not lead to central functional changes. Although the authors' studies show a strong correlation between GDx VCC parameters and axon loss in ExpG, this correlation may not always hold if acute axonal injury affecting birefringence precedes structural loss. Fortune et al. found that a decline in GDx parameters preceded retinal nerve fiber layer (RNFL) thickness changes in monkeys after optic nerve transection 36 and after intravitreal colchicine injection. 37 Thus, measures of birefringence may provide data on RNFL disease that are complementary to other imaging modalities. 
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Footnotes
 Supported by grants from NIH/NEI (R01 EY002698), (R01 EY014041), (P30 EY016665); Research to Prevent Blindness, Inc., New York, NY; unrestricted departmental and Physician–Scientist awards; Ocular Physiology Research and Education Foundation; and the Walter Helmerich Chair from the Retina Research Foundation.
Footnotes
 Disclosure: B.T. Gabelt, None; C.A. Rasmussen, None; O.Y. Tektas, None; C.B.Y. Kim, None; J.C. Peterson, None; T.M. Nork, None; J.N. Ver Hoeve, None; E. Lütjen-Drecoll, None; P.L. Kaufman, None
Figure 1.
 
Example of a GDx VCC scan from a monkey with ExpG. The GDx scan for monkey K560 shows severe thinning of the nerve fiber layers in the superior and inferior quadrants of the glaucomatous right eye (see also Table 2 for terminal GDx VCC values).
Figure 1.
 
Example of a GDx VCC scan from a monkey with ExpG. The GDx scan for monkey K560 shows severe thinning of the nerve fiber layers in the superior and inferior quadrants of the glaucomatous right eye (see also Table 2 for terminal GDx VCC values).
Figure 2.
 
TSNIT or average thickness changes in ExpG compared with Fellow eyes as a function of axon counts. Common GDx measures were highly correlated with percent change (%Δ) in axon counts in ExpG versus Fellow eyes (A, B) and with actual axon counts in ExpG eyes (C, D). The absolute value of GDx measures considering all eyes was also correlated with axon counts (E, F). Similar correlations were found with other GDx measures (superior average and inferior average). More axon count values were available for ExpG eyes than for Fellow eyes (open symbols indicate ExpG eyes where there were no corresponding Fellow eye axon counts, also see Table 4).
Figure 2.
 
TSNIT or average thickness changes in ExpG compared with Fellow eyes as a function of axon counts. Common GDx measures were highly correlated with percent change (%Δ) in axon counts in ExpG versus Fellow eyes (A, B) and with actual axon counts in ExpG eyes (C, D). The absolute value of GDx measures considering all eyes was also correlated with axon counts (E, F). Similar correlations were found with other GDx measures (superior average and inferior average). More axon count values were available for ExpG eyes than for Fellow eyes (open symbols indicate ExpG eyes where there were no corresponding Fellow eye axon counts, also see Table 4).
Figure 3.
 
Morphology of optic nerve damage as a result of ExpG. (AC) Schematic drawings showing typical distributions of severely damaged (red), slightly damaged (blue), and histologically unchanged (white) areas in eyes with axon counts of (A) approximately 800,000; (B) approximately 500,000 to 600,000; and (C) approximately 400,000–500,000. (DF) Semithin cross-sections of optic nerves (Richardson's stain). (D) Micrograph of a less damaged area (blue areas in the schematic drawings AC). The nerve fiber bundles are still separated from each other by connective tissue septae (arrows), which, at places, are thickened and show a thickened sheath of glial cells (asterisks). Singular axons are destroyed and appear as spherical inclusions of myelin figures (arrowheads). (E) Micrograph of a severely damaged area (red areas in the schematic drawings AC). Parts of the connective tissue septae appear destroyed (arrows) and displaced by numerous cells with large nuclei (asterisk). In the region of the previous bundles, remnants of myelin (arrowheads) are present. (F) Normal unaffected region of a nerve with the nerve fiber bundles separated from each other by connective tissue septae (arrows).
Figure 3.
 
Morphology of optic nerve damage as a result of ExpG. (AC) Schematic drawings showing typical distributions of severely damaged (red), slightly damaged (blue), and histologically unchanged (white) areas in eyes with axon counts of (A) approximately 800,000; (B) approximately 500,000 to 600,000; and (C) approximately 400,000–500,000. (DF) Semithin cross-sections of optic nerves (Richardson's stain). (D) Micrograph of a less damaged area (blue areas in the schematic drawings AC). The nerve fiber bundles are still separated from each other by connective tissue septae (arrows), which, at places, are thickened and show a thickened sheath of glial cells (asterisks). Singular axons are destroyed and appear as spherical inclusions of myelin figures (arrowheads). (E) Micrograph of a severely damaged area (red areas in the schematic drawings AC). Parts of the connective tissue septae appear destroyed (arrows) and displaced by numerous cells with large nuclei (asterisk). In the region of the previous bundles, remnants of myelin (arrowheads) are present. (F) Normal unaffected region of a nerve with the nerve fiber bundles separated from each other by connective tissue septae (arrows).
Table 1.
 
GDx VCC Parameters Versus c/d Changes in ExpG
Table 1.
 
GDx VCC Parameters Versus c/d Changes in ExpG
Δc/d
Control Eyes 0–0.1 0.15–0.2 ≥ 0.4
N = 9 N = 9 N = 7 N = 4
TSNIT ellipse avg. 52.96 ± 1.99 48.74 ± 1.52 47.55 ± 2.96 37.68 ± 3.80
Avg. thickness 45.00 ± 1.49 42.67 ± 1.11 41.86 ± 2.22 36.75 ± 2.95
Superior avg. 64.56 ± 2.99 61.28 ± 2.57 56.63 ± 4.54 40.37 ± 2.47
Inferior avg. 59.11 ± 2.74 55.48 ± 2.09 51.94 ± 3.82 39.57 ± 5.79
SD 22.80 ± 2.05 21.97 ± 1.31 18.30 ± 1.94 9.43 ± 1.87
Change from baseline
TSNIT ellipse avg. 0.10 ± 0.31 −3.86 ± 0.96* −6.12 ± 2.35* −12.74 ± 4.28
Avg. thickness −0.05 ± 0.28 −2.78 ± 1.04* −3.31 ± 1.83 −6.92 ± 4.12
Superior avg. 0.03 ± 0.46 −5.30 ± 1.89* −9.57 ± 3.02* −18.67 ± 4.61*
Inferior avg. 0.59 ± 0.53 −4.01 ± 1.39* −9.06 ± 3.22* −19.72 ± 5.51*
SD 0.19 ± 0.46 −2.95 ± 0.94* −6.73 ± 1.19* −14.30 ± 2.91*
Table 2.
 
Terminal GDx VCC Values for Axon Comparisons in Figure 2
Table 2.
 
Terminal GDx VCC Values for Axon Comparisons in Figure 2
GDx VCC Parameter (μm)
TSNIT (Ellipse Average) Average Thickness Superior Average Inferior Average
Monkey No. ExpG Cont ExpG Cont ExpG Cont ExpG Cont
K568 56.38 66.46 49.00 57.00 62.34 81.62 70.83 79.18
K639 37.67 55.23 36.00 47.00 44.67 63.73 41.20 61.11
K640 45.84 54.27 41.00 47.00 56.32 72.44 50.55 61.11
K560 31.02 53.38 30.00 46.00 42.10 62.30 25.94 60.89
K564 33.96 50.57 32.00 43.00 38.92 65.54 31.07 52.87
K576 42.48 47.06 40.00 42.00 39.34 39.21 51.31 53.41
K630 46.17 46.32 42.00 42.00 58.28 55.13 49.48 53.97
K645 50.07 52.63 44.00 46.00 68.48* 54.38 51.28 60.24
Table 3.
 
Terminal GDx VCC Parameters: No-Memantine Versus Memantine
Table 3.
 
Terminal GDx VCC Parameters: No-Memantine Versus Memantine
ExpG Fellow ExpG BL Fellow BL
No memantine (n = 7)
TSNIT 44.11 ± 3.77†‡ 55.20 ± 2.08* 50.69 ± 1.20 51.74 ± 1.61
Avg. thickness 39.00 ± 2.81†‡ 47.29 ± 1.90* 43.14 ± 1.24 44.14 ± 1.61
Superior avg. 52.62 ± 4.41*†‡ 67.99 ± 2.74* 62.32 ± 1.51 63.65 ± 1.57
Inferior avg. 50.08 ± 5.33 61.38 ± 3.16 57.30 ± 1.74 59.20 ± 2.75
Memantine (n = 8)
TSNIT 41.45 ± 2.58† 50.28 ± 1.47 49.77 ± 1.49 51.03 ± 1.46
Avg. thickness 37.25 ± 1.84† 43.38 ± 1.12 42.25 ± 1.15 44.08 ± 1.43
Superior avg. 50.69 ± 4.28 58.79 ± 3.44 62.77 ± 2.62 62.25 ± 1.87
Inferior avg. 43.74 ± 4.13*† 57.36 ± 2.26 57.10 ± 1.75 56.46 ± 1.64
Table 4.
 
Axon Counts: No-Memantine Versus Memantine
Table 4.
 
Axon Counts: No-Memantine Versus Memantine
Axon Count Total Optic Nerve Area (mm2) Septa Including Glia (% Optic Nerve Area) Connective Tissue Septa (% Optic Nerve Area)
Monkey No. ExpG Fellow ExpG Fellow ExpG Fellow ExpG Fellow
No memantine
K545 622,640 975,188 4.00 5.71 14.0 n.a. 1.64 1.75
K547 614,813 942,941 4.74 4.94 15.5 10.7 5.22 2.34
K640 823,680 n.a. 7.20 n.a. 10.0 n.a. 3.29 1.67
K568 746,941 922,756 4.38 4.27 8.7 9.4 1.96 2.00
K570 401,857 957,187 5.04 5.65 15.2 7.5 2.65 2.75
K581 563,581 1,053,519 3.97 5.43 16.0 n.a. 2.06 2.55
K639 667,722† 925,936 5.74 5.02 11.2 n.a. 2.83 2.50
Mean 634,462* 962,921 5.01 5.17 12.94 9.20 2.81 2.22
SEM 50,994 19,809 0.43 0.22 1.11 0.93 0.46 0.16
Memantine
K544 612,797 964,429 3.93 4.91 11.0 6.7 4.11 1.91
K549 802,935 n.a. 5.23 4.81 11.0 n.a. 3.61 3.26
K560 475,151 999,648 6.30 6.18 9.3 12.0 2.76 2.98
K564 474,918† 961,779 4.07 4.22 10.3 7.3 1.13 1.07
K576 818,209 n.a 6.51 6.09 14.5 n.a. 3.92 n.a.
K645 828,028† 943,033 5.11 5.90 25.6 16.2 5.60 4.33
K630 1,003,953 1,024,456 4.31 4.14 10.0 8.0 2.89 1.62
Mean 716,570* 990,179 5.07 5.18 13.10 10.04 3.43 2.53
SEM 70,022 16,602 0.39 0.33 2.18 1.80 0.52 0.49
Mean all 675,516* 976,550 5.04 5.17 13.02* 9.73 3.12* 2.36
SEM 45,275 12,989 0.28 0.20 1.17 1.13 0.34 0.24
Table 5.
 
Multifocal VEP K2.1 RMS SNR in ExpG and Fellow Eyes: Baseline and Terminal
Table 5.
 
Multifocal VEP K2.1 RMS SNR in ExpG and Fellow Eyes: Baseline and Terminal
Baseline RMS SNR Final RMS SNR
Monkey No. ExpG Fellow ExpG Fellow
No memantine
K543 5.906 4.522 4.350 3.204
K547 10.899 11.819 4.700 10.863
K568 6.355 5.491 4.795 4.039
K570 9.172 10.966 1.614 12.095
K574 5.920 5.333 3.378 9.475
K639 3.885 10.315 1.752‡ 7.638
K640 5.839 3.831 3.599 9.804
K625 8.379 5.081 5.052 6.465
Mean ± SEM 7.04 ± 0.85 7.17 ± 1.23 3.66 ± 0.51*† 7.95 ± 1.21
Memantine
K541 8.564 7.640 3.586 4.936
K544 7.665 5.106 2.685 11.751
K549 7.575 6.692 1.617 2.920
K560 5.009 6.064 8.554 8.105
K564 11.061 6.839 7.618‡ 3.586
K576 5.162 4.172 5.497 11.029
K630 3.802 11.533 4.470 6.237
K645 4.614 4.472 4.575‡ 2.062
K595 1.968 11.245 3.180 5.368
K608 3.944 2.035 1.708 2.613
Mean ± SEM 5.94 ± 0.91 6.58 ± 1.00 4.35 ± 0.78 5.86 ± 1.15
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