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The guinea pig is becoming an increasingly popular model for studying human myopia, which carries an increased risk of glaucoma. As a step towards understanding this association, this study sought to characterize the normal, developmental intraocular pressure (IOP) profiles, as well as the anatomy of the optic nerve head (ONH) and adjacent sclera of young guinea pigs. IOP was tracked in pigmented guinea pigs up to 3 months of age. One guinea pig was imaged in vivo with OCT and one with a fundus camera. The eyes of pigmented and albino guinea pigs (ages 2 months) were enucleated and sections from the posterior segment, including the ONH and surrounding sclera, processed for histological analyses - either hematoxylin and eosin (H&E) staining of paraffin embedded, sectioned tissue (n = 1), or cryostat sectioned tissue, processed for immunohistochemistry (n = 3), using primary antibodies against collagen types I-V, elastin, fibronectin and glial fibrillary acidic protein (GFAP). Transmission and scanning electron microscopy (TEM, SEM) studies of ONHs were also undertaken (n = 2 & 5 respectively). Mean IOPs ranged from 17.33 to 22.7 mmHg , increasing slightly across the age range studied, and the IOPs of individual animals also exhibited diurnal variations, peaking in the early morning (mean of 25.8, mmHg, ~9 am), and decreasing across the day. H&E-stained sections showed retinal ganglion cell axons organized into fascicles in the prelaminar and laminar region of the ONHs, with immunostained sections revealing collagen types I, III, IV and V, as well as elastin, GFAP and fibronectin in the ONHs. SEM revealed a well-defined lamina cribrosa (LC), with radially-oriented collagen beams. TEM revealed collagen fibrils surrounding non-myelinated nerve fiber bundles in the LC region, with myelination and decreased collagen posterior to the LC. The adjacent sclera comprised mainly crimped collagen fibers in a crisscross arrangement. Both the sclera and LC were qualitatively similar in structure in pigmented and albino guinea pigs. The well-organized, collagen-based LC of the guinea pig ONH is similar to that described for tree shrews and more similar to the human LC than that of other rodents that lack collagen. Based on these latter structural similarities the guinea pig would seem a promising model for investigating the relationship between myopia and glaucoma.
The guinea pig has become a popular model for the study of human myopia (Howlett and McFadden, 2006, 2009), which is now epidemic in some populations (Vitale et al., 2009). Myopia, or nearsightedness, refers to the condition in which light rays from distant objects come to focus in front of the retina, resulting in blurred retinal images when this focusing error is not corrected. In most cases, the mismatch between the eye's length and its refracting power is a result of the eye being longer than normal. Importantly, the risks of potentially blinding pathological complications, including retinal detachment, macular degeneration and primary open angle glaucoma (POAG) are closely associated with the amount of myopia (Casson et al., 2007; Jonas and Budde, 2005; Liang et al.; Xu et al., 2007b). As the prevalence of high myopia, commonly defined as greater than −6 D, has also risen along with myopia prevalence overall, high myopia is expected to result in a higher number of associated pathologies (Pan et al., 2013; Pierro et al., 1992). In addition, uncorrected myopia is a leading cause of functional blindness (Pascolini and Mariotti, 2012).
In relation to POAG, a number of studies have reported increased risks for myopes, by two- to three-fold, with high myopes being more at risk (Jonas and Budde, 2005; Mitchell et al., 1999). In the Beaver Dam study, it was found that compared to emmetropes, myopes recorded higher IOPs and were also 60% more likely to have POAG (Wong et al., 2003). While glaucoma appears to be a multi-factorial ocular disease, damage to the retinal ganglion cells (RGCs) and vision loss represent unifying end-points. Also of note in two recent studies, glaucomatous visual field damage and progression were found to be worse with increasing myopia (Perdicchi et al., 2007); optic nerve fiber loss was also more pronounced in highly myopic eyes than in less myopic eyes, implying greater susceptibility for optic nerve fiber damage in more myopic eyes, which also had larger optic discs (Jonas and Budde, 2005). Some of the evidence linking myopia with glaucoma and other sight-threatening pathologies is summarized in a recent review by Flitcroft (Flitcroft, 2012). However, note that some studies have reported no relationship between myopia and glaucoma progression in normal tension glaucoma (Sohn et al., 2010) and POAG (Hung et al., 2015).
In relation to nerve fiber loss in glaucoma, much attention has been paid to the lamina cribrosa (LC), which, in the human eye, is comprised of a collagenous meshwork spanning the scleral canal, deep in the optic nerve head, through which RGC axons pass to form the optic nerve. Changes in its structure have been strongly implicated in glaucomatous damage (Burgoyne et al., 2005; Quigley et al., 1983). Specifically, in glaucoma the LC is reported to deform, with the entire structure bowing posteriorly and its components compressed (Quigley et al., 1983; Yang et al., 2007). The deformation of the LC is postulated to generate shearing forces that disrupt critical transport processes within the axons of RGCs (Quigley et al., 1979; Sossi and Anderson, 1983). Other possible etiologies of axonal damage include impaired blood flow (Hayreh, 1969), laminar microarchitecture remodeling (Roberts et al., 2009), and biochemical alterations in extracellular matrix (Morrison et al., 1990). When IOP is artificially increased, the LC undergoes an anterior-posterior deformation, along with scleral canal expansion (Sigal et al., 2011), consistent with the suggestion that the biomechanical properties of the peripapillary sclera play an important role in the ONH changes in glaucoma (Girard et al., 2009a). Other glaucoma-related structural changes in the LC, specifically, increases in the area of laminar pores as well as shape changes (elongation) of the LC pores, have been observed in monkey eyes using advanced in vivo adaptive optics imaging (Vilupuru et al., 2007).
Of relevance to the current study, a previous study of enucleated highly myopic human eyes with and without glaucoma revealed the LCs of highly myopic eyes to be significantly thinner compared to those of less myopic eyes, and even thinner in highly myopic eyes with glaucoma (Jonas et al., 2004). The LCs of myopic eyes have also been reported to be more have more anterior surface irregularities (Miki et al., 2015). Either or both of these differences could contribute to the apparently greater susceptibility of myopes to glaucomatous optic disc changes (Fong et al., 1990; Scott and Grosvenor, 1993).
Of animal models used to study myopia, the chicken is one of the most widely used (Troilo et al., 1987; Wallman et al., 1987), yet it lacks a collagenous LC, and also lacks a concentration of astrocytic filaments in the retinal optic nerve junction (Morcos and Chan-Ling, 2000). Of animals currently being used for glaucoma research, well-organized collagenous LCs are present in the pig (Brooks et al., 1998), cat (Radius and Bade, 1982), dog (Brooks et al., 1989), and monkey (Gaasterland and Kupfer, 1974), but only one, the monkey, is also used as a myopia model.
While rodent models have been developed for many ocular diseases, including myopia and glaucoma (Faulkner et al., 2007; Gross et al., 2003), it is of interest that two of them, the mouse and rat, have non-collagenous LCs (Table 1)(Johansson, 1987; May and Lutjen-Drecoll, 2002). Astrocytes and oligodendrocytes represent the main non-neuronal, support component of the optic nerve head of rats and mice (Morcos and Chan-Ling, 2000). In a comprehensive study of OHN structures involving 18 different rodent species (Rodriguez-Ramos Fernandez and Dubielzig, 2013), the presence of an LC was confirmed in 4 species, including porcupine, capybara, flying squirrel and western gray squirrel, while the Norway rat and three species of mice were found to lack a LC. The lack of relevant histological sections of the optic nerve precluded evaluation of the LC for several species, including the guinea pig, which along with the mouse, also has application in myopia research. Nonetheless, several other studies have suggested that the guinea pig does have a LC, although its structure has not been studied in detail (Fujita et al., 2000; Furuta et al., 1993; Johansson, 1987). The study described here aimed to correct this deficiency – using a variety of microscopy techniques to fully characterize the ONH and adjacent sclera of nonmyopic guinea pig eyes, as well as to establish developmental intraocular pressure (IOP) profiles for the same.
Pigmented and albino guinea pigs were obtained from Elm Hill Labs (MA, USA). Albino animals were included because of their availability, reports of refractive error abnormalities (Jiang et al., 2014; Wang et al., 2007), and use in other ocular studies (Pucker et al., 2014). Animals were maintained on a 12-hour light/dark cycle and provided food and water ad libitum. For in vivo imaging, animals were anesthetized with ketamine (30 mg/ml) and xylazine (3 mg/ml). For in vitro studies of ocular tissue, animals were euthanized with an intracardial injection of sodium pentobarbital and eyes then enucleated and processed as described in detail below. The procedures used and numbers of animals used in each case are summarized in Table 2. Protocols were approved by the UC Berkeley and University of Houston Animal Care and Use Committees and conformed to the ARVO statement for the Use of Animals in Ophthalmic and Vision Research.
Pigmented guinea pigs (n=6) underwent intraocular pressure (IOP) measurements on a weekly basis from ages 2 to 7 weeks, then monthly up to 3 months of age. Measurements were always taken at the same time of day (afternoon), to avoid any confounding effect of diurnal rhythms. Guinea pigs were awake and handheld for measurement, which made use of a rebound tonometer, following manufacturer instructions and set to the rat calibration (TonoLab, Colonial Medical Supply, NH, USA). At each time point, three sets of six measurements were recorded on the right and left eyes, and averaged for each eye.
Diurnal IOP rhythms were evaluated in 12 adult pigmented guinea pigs (age 12-18 months). Using a rebound tonometer as described above, IOPs were recorded from their right eyes at two-hour intervals across a 24-hour period. Ten measurements were recorded at each time point and averaged. During the dark phase when lights were off (7:00 pm – 7:00 am), measurements were made in the dark using a dim red LED headlamp.
One 4 month-old pigmented guinea pig underwent in vivo fundus imaging. After pupil dilation with 2.5% phenylephrine and 1% tropicamide, fundus images were captured with a Visucam Pro NM fundus camera (Zeiss, Dublin, CA). Another 2 month-old pigmented guinea pig was imaged in vivo with spectral domain optical coherence tomography (SD-OCT, Bioptigen, NC, USA), which uses a wavelength of 840 nm, and a scan rate of approximately 32,000 A-scans per second, yielding a resolution better than 3 μm. Scan parameters included a 14 mm × 14 mm rectangle with 1000 A-scans per B-scan, 100 B-scans, and 3 B-scans per frame. For imaging, the guinea pig was anesthetized and positioned on a custom-built stage. A speculum was inserted in the eye to be imaged; the eye was then aligned with the optics of the instrument, the position of the reference arm adjusted appropriately to obtain a flat B-scan, a fundus image captured, and the retina then scanned using a custom rectangular volume protocol centered over the optic nerve head. Images were registered and averaged off-line.
Four different techniques were applied to characterize the optic nerve head architecture – standard histology with hematoxylin and eosin (H&E) staining applied to paraffin-embedded sections (n=1 pigmented eye), immunohistochemistry applied to cryostat sections (n=3 pigmented eyes), transmission electron microscopy (TEM; n=1 pigmented eye, n= 1 albino eye), and scanning electron microscopy (SEM; n=2 pigmented eyes, n= 3 albino eyes).
For H&E staining, one eye of a pigmented euthanized guinea pig was enucleated and fixed overnight in 4% paraformaldehyde. The eye then underwent dehydration and paraffin infiltration. Following sectioning, the slides were de-paraffinized with xylene and hydrated. The slides were stained with hematoxylin, rinsed, and stained with eosin. After a final dehydration, slides were mounted with coverslips and imaged.
For immunohistochemistry, the eyes of three euthanized pigmented guinea pigs (aged 2 months) were enucleated and fixed overnight at 4°C in a solution of 4% paraformaldehyde and 3% sucrose, then cryoprotected in 20% sucrose at 4°C for 6 h, before being embedded in a 1:1 solution of OCT and 20% sucrose and snap frozen with liquid nitrogen. Eight μm cryostat sections were cut from the posterior segment of the eye, which included the ONH. Sections including the proximal optic nerve were stained with primary antibodies for collagen types I-V, elastin, fibronectin and glial fibrillary acidic protein (GFAP), selected on the basis of the known composition of human, non-human primate, and tree shrew ONHs. After incubation in primary antibodies, the sections were then incubated in appropriate secondary AlexaFluor 488 antibodies. Images were captured using a DeltaVision Spectris deconvolution microscope (Applied Precision, Issequah, WA), as z-stacks through appropriate filters for DAPI and FITC fluorescence. Z-stacks were later deconvolved and shown as projections. As a control for nonspecific muscarinic staining, additional sections were prepared by omitting the primary antibody, then incubating the sections in the secondary antibody.
For both transmission and scanning electron microscopy (TEM and SEM, respectively), the optic nerve and surrounding 2 mm ring of sclera was collected from individual eyes and fixed with 2% gluteraldehyde. For TEM, the tissue underwent a 1% osmium tetroxide fixation followed by dehydration. Samples were then embedded in resin using a vacuum microwave infiltration method. Ultrathin sections were cut with a diamond knife and placed on grids. Samples were viewed using TEM (FEI Tecnai 12).
For SEM, the tissue then underwent alkali maceration with 10% NaOH for 48-76 h to remove cellular components, was rinsed and stained with 1% osmium tetroxide for 2 h, and then dehydrated through a graded ethanol series and critical point drying. Samples were mounted on aluminum stubs and imaged with an SEM (Hitachi TM-1000, Japan). Images were analyzed off-line with ImageJ (NIH, MD, USA), to determine maximum and minimum diameters and areas.
IOP data for right and left eyes are presented in Figure 1a. Values for the two eyes of individual animals were similar (p>0.05). Across the age range studied here, 2 weeks to 3 months, IOPs showed an early small increase and thereafter appeared to stabilize. This pattern is reflected in the following mean values of 17.6 ± 2.65 mmHg (mean ± SD) at 2 weeks of age and 22.7 ± 2.3 mmHg at 3 months of age. The means for individual eyes of individual animals ranged over the course of the 3-month study period from 17.3 to 25.7 mmHg.
Diurnal IOP data for right eyes of adults are shown in Figure 1b. The highest average IOP of 25.8 ± 2.5 mmHg (mean ± SE), was recorded at 9:00 am, with IOP thereafter decreasing across the day to a minimum at 9:00 pm of 20.1 ± 0.9 mmHg.
A representative normal fundus picture from a 4 months-old pigmented guinea pig is shown in Figure 2. The retina is largely avascular, allowing an uninterrupted view of the nerve fiber striations radiating from the optic nerve head (disc). In this example, the camera was focused on the nerve fiber layer, rendering the optic disc rim and cup slightly out-of-focus. The optic disc has distinct margins and a barely visible cup, with a network of fine blood vessels, which in this case, did not extend onto the neural retina.
Representative images captured using the Bioptogen SD-OCT instrument from another younger (2 months-old) pigmented guinea pig are shown in Figure 3. The low resolution, fundus image (Figure 3a) shows the optic nerve head and surrounding avascular retina, while the cross-sectional OCT image shows the various retinal layers, including the nerve fiber layer, which are readily visible, as is the retina-optic disc boundary, where Bruch's membrane terminates. The fine structural organization of the optic nerve cannot be resolved but were subsequently characterized from fixed tissue samples.
Nerve fibers traverse through the scleral opening to form the optic nerve, which expands in diameter after exiting the globe. The organization of retinal ganglion cell axons into fascicles begins in the prelaminar region, becoming more clearly defined in the laminar region, as evident in the H & E-stained sections of the ONH (Figure 4). Immunostained sections of the optic nerve head confirmed the presence collagen types I, III, IV and V, as well as elastin, GFAP and fibronectin in the structural elements of the ONH (Figure 5). Collagen also predominates in the fibrous sclera, which lies external to the choroid and is continuous with the dura mater surrounding the optic nerve.
TEM images of the guinea pig ONH revealed many parallels with the organization of the human ONH. In the prelaminar LC region, there are bundles of non-myelinated nerve fibers (retinal ganglion cell axons), surrounded by collagen fibrils (Figures 6A, D), while in the post-laminar region, the nerve axons are myelinated (Figures 6B, E). In the adjacent sclera, densely packed collagen fibrils are arranged in a criss-cross pattern. Images from the eyes of albino and pigmented animals were qualitatively similar in all respects.
SEM images of digested ONH preparations provided additional insight into the structural organization of the ONH, revealing a well-defined, multilayered lamina cribrosa, with radially-oriented bundles of connective tissue, including collagen beams (Figure 7). The central aggregation of collagen corresponds to the location of blood vessels visible in fundus images (Figure 2b), and presumably representing supporting collagenous sheaths. The scleral canals (openings) are elliptical in shape, with average dimensions of the longest and shortest axes of 352.4 ± 57.41 μm and 285.4 ± 34 μm respectively, corresponding to an average scleral canal area of 3.15 × 105 μm2. The orientation of the long and short axes of the ONH in the intact eye is not known, the nature of tissue processing precluding orientation markers being applied and retained in dissected optic nerve specimens. Here also there were no qualitative or quantitative differences between measurements obtained from pigmented and albino animals.
This study, which was largely focused on the structure of the optic nerve head in the guinea pig, found it to share many similarities in structure and biochemical composition to that of higher order mammals, non-human primates and humans. Specifically, the optic nerve head has a well-defined collagenous lamina cribrosa (LC), spanning the scleral opening, with the axons of retinal ganglion cells organized into fascicles, beginning in the pre-laminar region, and becoming myelinated as they emerge from the distal side of the LC. We elaborate on these comparisons in the following discussion as the basis for arguing that the guinea pig is a potentially valuable model for investigating the association between myopia and glaucoma.
Our findings for the guinea pig optic nerve head contrast with the descriptions for the mice and rats of non-collagenous optic nerve heads. Interestingly, while all belong to the rodentia class, it has often been argued that the guinea pig is, in fact, not a rodent (D'Erchia et al., 1996; Frederiksen and Heeno Andersen, 2003; Graur et al., 1991), with some suggesting that the guinea pig may have diverged before the separation of the primates from other rodents (Graur et al., 1991). It has also been noted that the mitochondrial genome of the guinea pig contradicts rodent monophyly (D'Erchia et al., 1996).
In terms of biochemical composition and structural organization, the optic nerve head of the guinea pig bears closest resemblance to the optic nerve head of the tree shrew. For example, the collagenous beams of the guinea pig LC were found to be radially arranged, similar to the pattern described for the tree shrew (Albon et al., 2007), although qualitatively, the beams appear to be less dense in the guinea pig ONH (Albon et al., 2007). As in the tree shrew, the guinea pig LC contains collagen types I, III, IV and V, and the ONHs of both species include elastin and glial fibrillary acidic protein (GFAP). Elastin is commonly found in connective tissue, where it plays an important role in allowing tissue to return to their usual shape after stretching. In the ONH, elastin may help to minimize the stress generated by the deforming influence of IOP on axons passing through the LC. GFAP, an intermediate filament protein, is a marker of glial cells. This protein is thought to contribute to the resilience and strength of astrocytes (Cullen et al., 2007), which have been shown to undergo reorientation in response to elevated IOP (Tehrani et al., 2014). It has thus been speculated that they play an important role in early glaucomatous optic nerve head changes. All of the above proteins have also been described in human ONHs (Albon et al., 1995; Hernandez et al., 1986; Morrison et al., 1989). These parallels are also important in the context of primary open angle glaucoma models; in humans, this disease causes elastin within the LC collagen beams to become disorganized and diminished (Quigley et al., 1991), and collagen type IV, normally localized to the septa, to extend into the nerve fiber bundles (Hernandez et al., 1990). While the magnification of antibody-labeled images in the current study (i.e., Figure 5) precluded localization of these various biochemical components, it was sufficient to confirm their presence in the optic nerve head.
In both humans and non-human primates, the collagen beams of the LC are surrounded by glial cells, forming channels that support the bundles of nerve fibers traversing the LC (Anderson, 1969; Furuta et al., 1993). H&E stained sections show numerous darkly stained nuclei outlining the surfaces of nerve fascicles, consistent with abundant GFAP labeling observed and thus a similar arrangement in the guinea pig ONH.
From SEM images, we were able to measure the dimensions of the scleral canal in a normal juvenile guinea pig; recorded diameters were also used to calculate a scleral canal area. However, these values are likely to underestimate in vivo dimensions, because of tissue shrinkage following fixation and dehydration, which may be as high as 20-30 percent (Johansson, 1987). Follow-up studies are warranted to characterize both changes in scleral canal size with age and with myopia, given that large ONHs, corresponding to large scleral canals, are known to be associated with early onset of glaucoma (Bellezza et al., 2003).
The LC is continuous with the sclera, which is intimately involved in myopic eye “growth” (enlargement), being the outer coat of the eye and ultimately the determinant of eye size (Rada et al., 2006). It thus seems plausible that the structure of the LC is also altered during myopic eye growth, and results from a number of different studies tend to be supportive of this idea. For example, like the LC, the parapapillary sclera of highly myopic human eyes is thinner than normal (Jonas et al., 2011) and the optic nerve heads of highly myopic eyes are reported to be different in appearance from those of eyes with lower myopia (Jonas et al., 1988; Xu et al., 2007a). In addition, longer eyes are associated with shallower LC depths, presumably due to changes in the scleral configuration with axial growth (Seo et al., 2014). It has been speculated that the posterior sclera exerts important biomechanical influences on the LC (Girard et al., 2009b; Norman et al.; Sigal et al.), and thus, it is of interest that in experimental myopia, increased eye elongation is associated with changes in both scleral composition (Gentle et al., 2003) and biomechanical properties (Siegwart and Norton, 1999). However, the LC has not been studied in a model of experimental myopia to-date.
One of the primary motivators for the current study was interest in finding a suitable animal model for studying the mechanism(s) underlying the apparent increased risk of primary open angle glaucoma in human myopes compared to non-myopes. The mouse, rat, rabbit and rhesus monkey are among the most widely used animal models of glaucoma and all have also been used in experimental myopia studies, albeit only on a limited scale in the case of the rabbit and rat (Barathi et al., 2008; Pickett-Seltner et al., 1988; Smith et al., 1987; Tokoro, 1970). Because the LC has been implicated in glaucomatous nerve damage, an animal model that possesses a collagenous LC is most relevant. However, of the above-mentioned animal models of glaucoma, neither the mouse, nor rat nor rabbit possess a collagenous LC. Although glaucoma can be induced in chickens through exposure to constant light (Kinnear et al., 1974), the chicken has not been widely used in glaucoma research, despite its wide use in myopia research. The presence in the chicken of an ocular pecten, which precludes direct visibility of the optic nerve head in vivo, represents one obstacle to its adoption. Thus by a process of elimination alone, it can be argued that the guinea pig represents a most promising model for investigating the link between myopia and glaucoma. While yet to be tested directly, it is expected that methods used to increase IOP in other animal models, for example, the microbead method used in mice (Frankfort et al., 2013), and laser trabeculoplasty, as used in non-human primate (Ivers et al., 2015), can be adapted for use in guinea pigs.
The majority of experiments described here involved relatively young, 2-4 month-old guinea pigs. Nonetheless, guinea pigs are precocial animals, being well developed at birth, and reaching sexual maturity early, around 2 months of age. Studies have shown that visual function is also well developed by 2 months of age (Ostrin et al, 2011, IOVS E-Abstract 6296)(Huang et al., 1990). Thus it is likely that the ONH structural characteristics closely approximate those of healthy adult animals.
As a side note, it must be acknowledged that the guinea pig possesses a largely avascular retina. However, in terms of glaucoma, the vascularity of the ONH is likely of greater importance. In this context, blood vessels have been described in the laminar beams of the guinea pig ONH in a previous study (Furuta et al., 1993), and the fundus image captured for this study (i.e., Figure 2b), represents further supporting evidence that the ONH of the guinea pig is vascularized. In addition, the fundus image shows a barely visible cup. It is yet to be established whether the cup becomes more visible with axonal loss, as observed in humans. Nonetheless, OCT imaging of nerve fiber layer was shown to be feasible in the guinea pig (i.e., Figure 3), and potentially offers an important, additional method of following the course of glaucomatous changes as well as evaluating structural changes associated with myopic eye growth.
A suitable animal model for glaucoma requires that IOP can be measured in an efficient, reliable manner and that the range of normal IOPs are similar to those reported in humans, as they determine, at least in part, the stresses experienced by the retinal ganglion cell axons as they pass through the LC. Our study made use of the TonoLab, a rebound tonometer calibrated for the rat eye, whereas another study involving guinea pigs made use of the TonoVet, a rebound tonometer calibrated for much larger animal eyes, i.e., dog, cat and horse (Tao et al., 2013). In that study, absolute values were also not reported, IOP data being described only in terms of statistical significance of differences between treated and fellow control eyes for given conditions. Two other studies involving guinea pigs made use of applanation tonometers (Coster et al., 2008; Williams and Sullivan, 2010). In the first study using a Tonopen applanation tonometer to measure 100 normal guinea pigs (age unknown), an average IOP of 16.5 ± 3.2 mmHg was reported (Williams and Sullivan, 2010), similar to the mean IOP of our 2 weeks-old animals (17.6 ± 2.6 mmHg), but significantly lower than our mean value for older animals (22.7 ± 2.3 mmHg). The other study using applanation tonometry reported a mean IOP of 18.27 ± 4.55 mmHg for 31 normal guinea pigs (age unknown)(Coster et al., 2008). In both of these studies, measurements were made in awake animals using a topical anesthetic. Note that while our study used a TonoLab, we found results to be no different from those collected with a Tonopen in a study of 30 guinea pig eyes (data not shown, p = 0.87). While manometric calibration for the guinea pig eyes is currently lacking for both instruments, the range of recorded IOP values are consistent with normal ranges reported for other animals. In our study, we also avoided the use of general anesthesia, after confirming in a pilot study that general anesthesia induced with ketamine/xylazine has a profound hypotensive effect, just as reported in other animals; measurements made on guinea pigs recovering from this anesthesia averaged 13.17 mmHg. Our choice of instrument had the added advantage of avoiding the need for topical corneal anesthesia.
In summary, this study showed that the ONH of guinea pig has a well-organized, collagen-based LC, similar in composition to that of humans. Thus, as a substitute for primate models, the guinea pig shows promise as a model for human ocular diseases that are known to affect the ONH, including myopia and glaucoma.
NIH NEI K08 EY022696 to LO and NIH NEI R01 EY012392 to CW, Thanks to Jessie Lee for assistance with TEM imaging
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